Skip to main content

Main menu

  • Home
  • Current Issue
  • Archive
  • Info for
    • Authors
    • Editorial Policies
    • Subscribers
    • Advertisers
    • Editorial Board
    • Special Issues 2025
  • Journal Metrics
  • Other Publications
    • In Vivo
    • Cancer Genomics & Proteomics
    • Cancer Diagnosis & Prognosis
  • More
    • IIAR
    • Conferences
    • 2008 Nobel Laureates
  • About Us
    • General Policy
    • Contact
  • Other Publications
    • Anticancer Research
    • In Vivo
    • Cancer Genomics & Proteomics

User menu

  • Register
  • Subscribe
  • My alerts
  • Log in
  • My Cart

Search

  • Advanced search
Anticancer Research
  • Other Publications
    • Anticancer Research
    • In Vivo
    • Cancer Genomics & Proteomics
  • Register
  • Subscribe
  • My alerts
  • Log in
  • My Cart
Anticancer Research

Advanced Search

  • Home
  • Current Issue
  • Archive
  • Info for
    • Authors
    • Editorial Policies
    • Subscribers
    • Advertisers
    • Editorial Board
    • Special Issues 2025
  • Journal Metrics
  • Other Publications
    • In Vivo
    • Cancer Genomics & Proteomics
    • Cancer Diagnosis & Prognosis
  • More
    • IIAR
    • Conferences
    • 2008 Nobel Laureates
  • About Us
    • General Policy
    • Contact
  • Visit us on Facebook
  • Follow us on Linkedin
Review ArticleReview
Open Access

Sun Exposure - Hazards and Benefits

PELLE G. LINDQVIST, ELISABETH EPSTEIN and MONA LANDIN-OLSSON
Anticancer Research April 2022, 42 (4) 1671-1677; DOI: https://doi.org/10.21873/anticanres.15644
PELLE G. LINDQVIST
1Department of Obstetrics and Gynecology, Södersjukhuset, and Department of Clinical Sciences and Education, Karolinska Institute, Stockholm, Sweden;
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: Pelle.lindqvist@ki.se
ELISABETH EPSTEIN
1Department of Obstetrics and Gynecology, Södersjukhuset, and Department of Clinical Sciences and Education, Karolinska Institute, Stockholm, Sweden;
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
MONA LANDIN-OLSSON
2Department of Endocrinology, Clinical Sciences, Lund University, Lund, Sweden
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & Metrics
  • PDF
Loading

Abstract

There are carcinogenic effects of sun exposure that increase the risk for skin cancer, especially for fair-skinned individuals. Therefore, there are recommendations to avoid sun exposure and to apply sun blockers. A more nuanced and balanced message for sun safety guidelines is now advocated. Despite an increased risk of death due to skin cancer, fair skinned women seem to have an overall survival advantage. In addition, an inverse association between sun exposure and hypertension, thromboembolism, and type 2 diabetes mellitus has been shown. Furthermore, low sun exposure habits result in increased risk of cardiovascular disease (CVD), and non-CVD/non-cancer mortality among women. There are also data supporting that the prognosis of cancer is improved with increasing levels of vitamin D/sun exposure. In this narrative review we will provide a brief update of hazards and benefits of sun exposure focused on an updated, balanced, and evidence-based view.

Key Words:
  • UV exposure
  • diabetes mellitus
  • cancer
  • melanoma
  • cardiovascular disease
  • mortality
  • review

A US National Cancer Institute sponsored interdisciplinary meeting was gathered in 2016 to improve sun protection guidelines (1). Among other, they called for nuanced messages for at-risk populations, that reducing risk for one disease should not come at the cost of increasing risk for another. They concluded that although harms associated with overexposure of sun outweigh the benefits and should be avoided, the beneficial effects of ultraviolet radiation (UVR) exposure should not be ignored in developing new sun safety guidelines (1).

MISS Cohort

Our studies are mainly performed within the large melanoma in southern Sweden (MISS) cohort (2). Since 1990, we have followed ~30,000 women with written questionnaires every 10 years. We included ~750 Swedish-born women from each year between 1927 and 1966, without a diagnosis of cancer at inclusion. The women were randomized from the Swedish population registry and comprise 20% of the south Swedish population in the selected age-groups. By means of personal identification number (PIN) it was possible to crosslink data from the National prescription register and National discharge register. The rate of dropouts was neglectable. The few women who emigrated remained in the study until emigration.

Sun exposure habits are related to exercise, body mass index (BMI), skin color, and socio-economic factors. We have therefore adjusted for these variables in order to compensate for confounding factors. We used odds ratio as a measure of risk. Sweden is a country at latitude 55° to 68° North with scarcity of sun, and there are only few days per year when ultraviolet (UV) index is >6 and more than half of the year the UV index is ≤3.

Our studies based on a prospective cohort design will not give causal results, but only hypothesis generating associations that may suggest causality. The finding of dose-dependency, correct temporal and consistency of association’s effect, and a plausible relationship in a prospective cohort study increase the likelihood of causality. Similar data as other well-established relationships or experimental research may provide additional support. A prospective cohort study has advantage over retrospective cohort or case-control studies due to the correct baseline status and independence from recall data.

In contrast to most other sun exposure studies, we were not interested in those with highest exposure habits, but instead the group with the lowest habits. We assessed low sun exposure as the possible 4th major lifestyle factor for our health, together with low exercise habits, smoking, and obesity. In these MISS studies, we categorized sun exposure according to the answer to four selected questions; Do you sunbath during summer? Do you travel south to sun bath? Do you use solarium? Do you sunbath during winter vacations? Women answering no to all of these questions were categorized as having low sun exposure habits, one or two “yes” as moderate sun exposure and “yes” to three or four as greatest sun exposure habits. Self-reported UVR levels have been shown to better predict objectively measured UVR compared to ambient UVR (3).

Skin Cancer and Cancer Mortality

UVR is the most important environmental risk factor for both cutaneous malignant melanoma (MM) and non-melanoma skin cancer (NMSC). The risk factor for NMSC is mainly the cumulative UV exposure and NMSC is rarely a risk factor for death. MM is caused mainly by overexposure to UVR. Sun exposure and solarium are the dominant sources of UV exposure and high UV exposure is estimated to increase the risk of MM up to 2-fold. In our 20-year follow-up, the total incidence of MM was 0.9%, 0.81% for low and 1.1% for greatest exposure (OR=1.34, 95%CI=0.8-2.3) (4).

In the MISS cohort, women who used solarium were at a 20% increased risk of MM [hazard ratio (HR)=1.2, 95%CI=1.0-1.6], but the risk of all-cause mortality was 23% lower (HR=0.77, 95%CI=0.7-0.8) as compared to those that did not use solarium (5). In the MISS study, there was a dose-dependent increase in the risk of death with lower exposure, with a 40% higher risk of cancer-related death in the group with low sun exposure [subHR (sHR)=1.4, 95%CI=1.04-1.6] as compared to those with greatest sun exposure (4).

The incidence of MM is rising 5% annually, while the age standardized total risk of death decreases annually by 2.2% (6). In 2016, the risk for women to be diagnosed with MM in Sweden before the age of 75 was estimated to be 2.3%, comprising 6.6% of all cancers and 2.2% of cancer-related deaths (6). Thus, in terms of cancer mortality, MM is a small contributor to death (6). The mortality rate during the study interval of women who developed MM differed between sun exposure groups, low sun exposure 36%, moderate sun exposure 16%, and greatest sun exposure 11% (4). Thus, women with more active sun exposure habits survived their MM more often. Newton Bishop and co-workers reported the HR for relapse-free survival of MM was 0.79 (95%CI=0.64-0.96; p=0.01) for each 20 nmol/l increase in plasma vitamin D levels (7). An Italian study reported that sun bathing holidays after a diagnosis of MM were related to reduced rates of relapses (HR=0.3, 95%CI=0.1-0.9) (8).

Our results of lower death rate among those with high sun exposure are not new. Already in 1937, Peller and Stephenson reported that soldiers of US Navy, intensively exposed to open air, sun rays, and salt water, had 8-fold higher frequency of skin cancer (MM) and lip cancer, but the death rate among these cases of cancer was 3-fold lower than expected. In addition, they reported a 44% lower incidence of other cancer-related deaths (9).

In agreement with the above, those included in the VITAL trial (n=25871) in the vitamin D arm (2000 U vitamin D daily for 5 years) showed a 25% reduction of death due to cancer (HR=0.75, 95%CI=0.59-0.96), but vitamin D had no effect on incidence (10). Supplementation with 2000 U raised the vitamin D level in the plasma approximately 27 nmol/l from a baseline of ~77 nmol/l. This was followed-up with a meta-analysis of randomized controlled trials (RCT’s) with vitamin D supplementation, that showed no effect on cancer incidence, but a 13% reduced risk of cancer death (HR=0.87, 95%CI=0.79-0.96) among those supplemented with vitamin D (11). The authors suggest that we should aim for vitamin D levels of 54-135 nmol/l in the plasma to reduce cancer mortality. Possible mechanisms for this improved prognosis are decreased invasiveness and immunomodulatory effects of vitamin D (12). Since UV is a carcinogen, inappropriate overexposure should be avoided. However, paradoxically, although sun exposure is the major risk factor for MM, the incidence of death due to cancer is lower among those with greatest exposure, possibly due to improved prognosis. Vitamin D seems to be involved in cancer prognosis, but not cancer incidence.

Redheads or Fair Skin

Red hair, freckles, pale skin, and melanocytic nevus are all genetically determined risk factors for MM, occurring most frequently among Irish, Scottish, and Scandinavian populations (13). The reason for prevalent skin risk factors in the North is presumably due to the evolutionary selection of a sun sensitive skin in these countries because of the low UV intensity. However, UVR may not be an important risk factor for MM among those with skin of color (14). In a recent study, we matched 11993 fair (redhead or having freckles) women one-to-one to non-fair white women and adjusted for age, smoking, education, marital status, income, and comorbidity. We aimed to assess whether fair women had a survival advantage and whether they had an over-risk of death due to skin cancer (15). We found that fair women had a 59% increased risk of death due to skin cancer (OR=1.59, 95%CI=1.3-2.0) while having an 8% overall longer life expectancy (OR=1.08, 95%CI=1.002-1.2) (15). The increase in risk for NMSC among fair women in our study was somewhat lower (OR=1.6, 95%CI=1.3-1.9) than previously reported for other populations (OR=2.0, 95%CI=1.7-2.4) (15, 16). The odds of MM were also lower (OR=1.3, 95%CI=1.03-1.65 vs. 2.4 95%CI=1.7-3.4, respectively) (15, 17).

Our interpretation is that sun sensitive skin is selected in Northern Europe by evolution and the increased risk of skin cancer is the “cost” for this survival advantage. Our conclusion is that fair women should not abstain from sunlight, but they do not need as much sun exposure as non-fair women.

Sunscreen Use

Sunscreen users in Sweden have been reported to be at an 80% increased risk of MM (OR=1.8, 95%CI=1.1-2.9) (18). The subgroup of 19% of women who used sunscreen to enable long time exposure to the sun was at an 8-fold increased risk of MM (OR=8.5, 95%CI=1.0-75.8) (18). A plausible explanation of this increased MM risk might be that the application of a sunscreen inhibits the redness of the skin but allows prolonged UV exposure (=overexposure). Further, this subgroup usually applies low sun protection factor (SPF), while those who use sunscreens for other reasons use higher SPF (18). Only one Lóreal sponsored RCT has shown a 50% reduction (n=11 vs. n=22) of MM (19), but population-based cohort studies have shown increased risk (20). It has been difficult to assess whether sunscreen-use protects against MM or not (20). There is a general agreement that overexposure to UVR should be avoided.

In relation to the National Cancer Institute’s call, it might be effective to address the above highest-risk group who used sunscreen to enable long time exposure to the sun and recommend not to overexpose (1). The prior one size-fits-all approach only focusing on sunscreen use, might give a false sensation of security, explaining part of the rise in MM incidence. Daily short sun exposure, at mid-day, without the use of sunscreens, might be optimal for health. Fair individuals need less sun exposure than those with more pigmented skin (15). A too restrictive sun exposure advice might do more harm than good by increasing the risk of death due to other diseases such as myocardial infarction and stroke (4). Sweden is a country with scarcity of sun; advice will presumably differ in countries with higher UV intensity.

Type 2 Diabetes Mellitus (T2DM)

In 2010, we reported observational evidence of an inverse dose-dependent association to T2DM frequency with increasing sun exposure (21). We showed that the decrease in risk for T2DM was still significant after adjusting for exercise and smoking habits. The risk reduction was inversely associated to BMI, with 40% to 60% reduction of T2DM among lean, 20% to 40% among overweight, and no risk reduction in the obese subgroup (21). A similar relationship with BMI is seen in the risk of endometrial cancer (22). Experimental research on mice given a diabetogenic diet together with long-term sub-erythemal UVR indicated not only an increase in glucose tolerance and decrease in insulin resistance but also suppression of weight gain and cholesterol levels (23). In addition, UVR exposure of obese mice reduced risk factors for cardio-metabolic dysfunction and weight (24, 25).

The relationship between vitamin D and T2DM have attained much interest. Low levels of vitamin D in the plasma in women are associated with high incidence of both T2DM and gestational diabetes (26–28). However, supplementation with 4000 U vitamin D did not lower the incidence of T2DM significantly (29). In Sweden, half of pregnant women are low in vitamin D and an even greater proportion during the winter season (30). Women with active sun exposure habits are reported to have normal vitamin D levels the whole year (31). In response to UV exposure, the increase in vitamin D in the plasma is lower among obese as compared to lean individuals, and there is an inverse relationship between BMI and vitamin D levels (28, 32). A large study using bidirectional Mendelian randomization analysis showed that higher BMI leads to lower vitamin D in the plasma, while the likelihood of low vitamin D levels to increase BMI is small (33). Thus, BMI seems to be in the causal pathway between sun exposure/vitamin D and health effects (33). The association between the adipose tissue and vitamin D levels in the plasma need to be further elucidated.

The low vitamin D values, constantly seen in T2DM cohorts, might be a marker of low sun exposure or an effect of increased BMI/adipose tissue. Sun exposure has additional effects apart from vitamin D production such as an effect on systemic inflammation, immunomodulation, melatonin system, nitric oxide, and calcium transport. In addition, low levels of sun exposure/vitamin D might also be a marker for an unhealthy lifestyle that precedes the diagnosis of T2DM. The combination of similar hypothesis generating and experimental results increase the likelihood of a causal inverse relationship between sun exposure and T2DM.

Cardiovascular Disease (CVD) and CVD Mortality

Venous thromboembolism. We have assessed the risk of venous thromboembolic events (VTE) during 11 years in the MISS cohort (2). For every “yes” of the four questions of sun exposure, the risk of VTE decreased by approximately 30%. The risk of VTE was approximately 50% higher in winter compared to summer. Women with a presence of VTE were at a 4-fold higher risk of being diagnosed with a cancer during the study period. Women with a prior use of combined oral contraceptives were at a significantly 30% lower risk of VTE (2).

Several studies have showed an inverse relationship between vitamin D levels and VTEs (34). Low vitamin D levels have been shown to be associated with increased interleukin 6 (IL-6), homocysteine, plasminogen activator inhibitor-1 (PAI-1), and tissue factor pathway inhibitor (TFPI) levels (35). There is need of experimental studies exploring the relationship between UV exposure, plasma levels of vitamin D, coagulation system and thromboembolism. During the last 10 years, lifestyle advice in the Swedish guidelines for pregnant women at increased risk of thromboembolism has included active sun exposure habits (36).

Hypertension and cardiovascular (CVD) mortality. Hypertension is the major modifiable driver for morbidity and mortality (37) and a procedure that would lower blood pressure on a population level would produce a major difference to the burden of diseases. There are several experimental studies showing a transient effect of UVR on blood pressure, but studies to date have been small and have given divergent results (38–42). Two population based studies report an inverse relationship between ambient UVR and systolic blood pressure (43, 44), with a 59% increased risk of stroke in areas below the median of ambient UVR, as compared to above (43). The effect on blood pressure was reported to be independent of plasma vitamin D (43, 45). A Chinese study reported that women who sunbathed 30 minutes per day had a 40% lower risk of hypertension (46). In a Saudi Arabian study of overweight patients, the prevalence of hypertension decreased from 28.1% to 11.1%, blood pressure decreased from a mean of 118.3/76.0 to 112.6/73.9 and the mean BMI dropped, after recommendation of increased dietary vitamins and 5 to 30 minutes of sun exposure twice a week during one year (47). A recent study comprising dialysis patients in the US shows that higher incident UVR was associated with lower blood pressure (48).

A major breakthrough of our understanding of a possible effect of sun exposure was when Liu and coworkers presented an alternative explanation for the known inverse association between vitamin D levels in the plasma and CVD risk (39, 49). They showed skin mobilization of nitric oxide (NO) in response to UVA radiation, not depending of circulatory nitric oxide synthases (NOS), which caused transient blood pressure reduction through photolysis of cutaneous nitrite or nitrate (39). They suggested vitamin D levels to be a biomarker for sunlight exposure (39). Recently, we assessed whether the level of sun exposure was associated with being treated for hypertension within the MISS cohort (50). In Sweden, all prescription drugs are recorded into a central registry since 2005. The reported sun exposure habits from the questionnaire year 2000 and all antihypertensives prescribed on an individual basis that were registered between 2005 and 2007 were accessed, and all women who had had at least one prescription were considered to have hypertension (n=23,593). Thus, we used prescription of antihypertensive medication as a proxy for hypertension. As compared to the group with greatest sun exposure, those with lowest and moderate sun exposure were at 41% and 15% greater odds of being on hypertensive medication five to seven years later (OR=1.41, 95%CI=1.3-1.6 and OR=1.15, 95%CI=1.1-1.2). There was an age-related ~two-fold increased risk per 10-year increase in age. Other risk factors were lack of exercise 36% increased (OR=1.36, 95%CI=1.2-1.5), non-fair phenotype 8% increased (OR=1.08, 95%CI=1.01-1.15), high chronic stress-related comorbidity 80% increased (OR=1.8, 95%CI=1.4-2.3), lack of university schooling 30% increased (OR=1.3, 95%CI=1.3-1.4) odds of being on antihypertensive medication (50). A Swiss population-based study showed decreasing CVD mortality with increasing altitude, 20% per 1,000 m for coronary heart disease and 12% per 1,000 m for stroke (51). The authors concluded that this was not due to established risk factors and suggested it might be due to the weather (higher UV exposure). In our competing risk analysis, we showed that the risk of CVD mortality was highest among those with low sun exposure habits [60% increased (sHR=1.6, 95%CI=1.3-2.0)](4). As compared to those with the highest sun exposure habits, those with moderate and low were at 50% and 130% increased risk of death within the study interval of 20 years (sHR=1.5, 95%CI=1.2-2.8, and sHR=2.3, 95%CI=1.8-3.1, respectively) (4).

The combination of experimental transient decrease in blood pressure by UVR and a dose-dependent decreased risk antihypertensive medication and CVD mortality with increasing sun exposure increase the likelihood of a causal relationship between sun exposure and CVD. However, effect from confounding factors cannot be excluded.

Non-cancer/non-CVD. In our competing risk analysis, we showed the risk of non-cancer/non-CVD mortality was highest among those with low or moderate sun exposure habits. These women were at 70% increased risk of death (sHR=1.7, 95%CI=1.4-2.1) (4), as compared to those with the highest sun exposure habits. Those with moderate and low sun exposure habits were at 60% and 110% increased risk of death within the study interval of 20 years (sHR=1.6, 95%CI=1.3-1.9, and sHR=2.1, 95%CI=1.7-2.8, respectively) (4).

All-cause Mortality and Sun Exposure

Yang and coworkers showed in 2011 that those having > 1 week of sun bathing holiday for 20-30 years were at 30% lower all-cause mortality compared to their background population (52). We showed a dose-dependent inverse relationship between sun exposure and all-cause mortality, with doubled risk among those with low, compared to greatest sun exposure (HR=2.0, 95%CI=1.6-2.5) (5). In our competing risk analysis, smokers had a higher death ratio within the study interval. When also stratifying for sun exposure habits, non-smokers with low sun exposure had a similar death rate as smokers with greatest sun exposure, in each age-interval. We draw the conclusion that low sun exposure is a risk factor for death in the same magnitude as smoking (4). In addition, as compared to those with the greatest sun exposure, woman with age > 55 and low sun exposure had 1 month shorter life expectancy, per year (15). Since we all will die from some cause and the greatest reductions in risk of death were in the CVD and non-cancer/non-CVD groups, death due to cancer will increase. If we live 2-3 years longer, we will increase the risk of attaining a cancer and die from it. However, the age-standardized risk of death due to cancer will not increase.

Conclusion

There is an established relationship between sun exposure and an increased risk of skin cancer. This risk is further increased among fair women, but these women seem to have a survival advantage. There seem to be an inverse association between sun exposure and hypertension, T2DM, venous thromboembolism, CVD, and cancer prognosis. All of these effects might explain the inverse association between sun exposure and all-cause mortality. Both vitamin D and NO seem to be major contributors to the above effects. Although, our results are not in opposition to the results of others, confounding factors cannot be excluded.

Footnotes

  • Authors’ Contributions

    Conception and design of the study: PLT, EE and MLO. Analysis and interpretation of data: PLT. Collection and assembly of data: PLT, EE and MLO, Drafting of the article: PLT, Critical revision and final approval of the article: PLT, EE and MLO.

  • Conflicts of Interest

    The Authors have no competing interests in relation to this study.

  • Received January 13, 2022.
  • Revision received February 24, 2022.
  • Accepted February 25, 2022.
  • Copyright © 2022 The Author(s). Published by the International Institute of Anticancer Research.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY-NC-ND) 4.0 international license (https://creativecommons.org/licenses/by-nc-nd/4.0).

References

  1. ↵
    1. Geller AC,
    2. Jablonski NG,
    3. Pagoto SL,
    4. Hay JL,
    5. Hillhouse J,
    6. Buller DB,
    7. Kenney WL,
    8. Robinson JK,
    9. Weller RB,
    10. Moreno MA,
    11. Gilchrest BA,
    12. Sinclair C,
    13. Arndt J,
    14. Taber JM,
    15. Morris KL,
    16. Dwyer LA,
    17. Perna FM,
    18. Klein WMP and
    19. Suls J
    : Interdisciplinary perspectives on sun safety. JAMA Dermatol 154(1): 88-92, 2018. PMID: 29117315. DOI: 10.1001/jamadermatol.2017.4201
    OpenUrlCrossRefPubMed
  2. ↵
    1. Lindqvist PG,
    2. Epstein E and
    3. Olsson H
    : Does an active sun exposure habit lower the risk of venous thrombotic events? A D-lightful hypothesis. J Thromb Haemost 7(4): 605-610, 2009. PMID: 19335448. DOI: 10.1111/j.1538-7836.2009.03312.x
    OpenUrlCrossRefPubMed
  3. ↵
    1. Soueid L,
    2. Triguero-Mas M,
    3. Dalmau A,
    4. Barrera-Gómez J,
    5. Alonso L,
    6. Basagaña X,
    7. Thieden E,
    8. Wulf HC,
    9. Diffey B,
    10. Young AR,
    11. Nieuwenhuijsen M and
    12. Dadvand P
    : Estimating personal solar ultraviolet radiation exposure through time spent outdoors, ambient levels and modelling approaches. Br J Dermatol 186(2): 266-273, 2022. PMID: 34403140. DOI: 10.1111/bjd.20703
    OpenUrlCrossRefPubMed
  4. ↵
    1. Lindqvist PG,
    2. Epstein E,
    3. Nielsen K,
    4. Landin-Olsson M,
    5. Ingvar C and
    6. Olsson H
    : Avoidance of sun exposure as a risk factor for major causes of death: a competing risk analysis of the Melanoma in Southern Sweden cohort. J Intern Med 280(4): 375-387, 2016. PMID: 26992108. DOI: 10.1111/joim.12496
    OpenUrlCrossRefPubMed
  5. ↵
    1. Lindqvist PG,
    2. Epstein E,
    3. Landin-Olsson M,
    4. Ingvar C,
    5. Nielsen K,
    6. Stenbeck M and
    7. Olsson H
    : Avoidance of sun exposure is a risk factor for all-cause mortality: results from the Melanoma in Southern Sweden cohort. J Intern Med 276(1): 77-86, 2014. PMID: 24697969. DOI: 10.1111/joim.12251
    OpenUrlCrossRefPubMed
  6. ↵
    1. Custom Nordscan, Projektet NORDCAN
    . The Association of the Nordic Cancer Registries (ANCR); 2012 to 2016. Available at: https://www-dep.iarc.fr/nordcan/sw/frame.asp [Last accessed on February 25, 2022]
  7. ↵
    1. Newton-Bishop JA,
    2. Beswick S,
    3. Randerson-Moor J,
    4. Chang YM,
    5. Affleck P,
    6. Elliott F,
    7. Chan M,
    8. Leake S,
    9. Karpavicius B,
    10. Haynes S,
    11. Kukalizch K,
    12. Whitaker L,
    13. Jackson S,
    14. Gerry E,
    15. Nolan C,
    16. Bertram C,
    17. Marsden J,
    18. Elder DE,
    19. Barrett JH and
    20. Bishop DT
    : Serum 25-hydroxyvitamin D3 levels are associated with breslow thickness at presentation and survival from melanoma. J Clin Oncol 27(32): 5439-5444, 2009. PMID: 19770375. DOI: 10.1200/JCO.2009.22.1135
    OpenUrlAbstract/FREE Full Text
  8. ↵
    1. Gandini S,
    2. De Vries E,
    3. Tosti G,
    4. Botteri E,
    5. Spadola G,
    6. Maisonneuve P,
    7. Martinoli C,
    8. Joosse A,
    9. Ferrucci PF,
    10. Baldini F,
    11. Cocorocchio E,
    12. Pennacchioli E,
    13. Cataldo F,
    14. Bazolli B,
    15. Clerici A,
    16. Barberis M,
    17. Bataille V and
    18. Testori A
    : Sunny holidays before and after melanoma diagnosis are respectively associated with lower Breslow thickness and lower relapse rates in Italy. PLoS One 8(11): e78820, 2013. PMID: 24223851. DOI: 10.1371/journal.pone.0078820
    OpenUrlCrossRefPubMed
  9. ↵
    1. Peller S and
    2. Stephenson CS
    : Skin irritation and cancer in the United States Navy. Am J M Sc 194: 326-333, 1937.
    OpenUrlCrossRef
  10. ↵
    1. Manson JE,
    2. Cook NR,
    3. Lee IM,
    4. Christen W,
    5. Bassuk SS,
    6. Mora S,
    7. Gibson H,
    8. Gordon D,
    9. Copeland T,
    10. D’Agostino D,
    11. Friedenberg G,
    12. Ridge C,
    13. Bubes V,
    14. Giovannucci EL,
    15. Willett WC,
    16. Buring JE and VITAL Research Group
    : Vitamin D supplements and prevention of cancer and cardiovascular disease. N Engl J Med 380(1): 33-44, 2019. PMID: 30415629. DOI: 10.1056/NEJMoa1809944
    OpenUrlCrossRefPubMed
  11. ↵
    1. Keum N,
    2. Lee DH,
    3. Greenwood DC,
    4. Manson JE and
    5. Giovannucci E
    : Vitamin D supplementation and total cancer incidence and mortality: a meta-analysis of randomized controlled trials. Ann Oncol 30(5): 733-743, 2019. PMID: 30796437. DOI: 10.1093/annonc/mdz059
    OpenUrlCrossRefPubMed
  12. ↵
    1. Brożyna AA,
    2. Hoffman RM and
    3. Slominski AT
    : Relevance of vitamin D in melanoma development, progression and therapy. Anticancer Res 40(1): 473-489, 2020. PMID: 31892603. DOI: 10.21873/anticanres.13976
    OpenUrlAbstract/FREE Full Text
  13. ↵
    1. Newton-Bishop J,
    2. Bishop DT and
    3. Harland M
    : Melanoma genomics. Acta Derm Venereol 100(11): adv00138, 2020. PMID: 32346746. DOI: 10.2340/00015555-3493
    OpenUrlCrossRefPubMed
  14. ↵
    1. Lopes FCPS,
    2. Sleiman MG,
    3. Sebastian K,
    4. Bogucka R,
    5. Jacobs EA and
    6. Adamson AS
    : UV exposure and the risk of cutaneous melanoma in skin of color: a systematic review. JAMA Dermatol 157(2): 213-219, 2021. PMID: 33325988. DOI: 10.1001/jamadermatol.2020.4616
    OpenUrlCrossRefPubMed
  15. ↵
    1. Lindqvist PG,
    2. Epstein E,
    3. Landin-Olsson M,
    4. Åkerlund M and
    5. Olsson H
    : Women with fair phenotypes seem to confer a survival advantage in a low UV milieu. A nested matched case control study. PLoS One 15(1): e0228582, 2020. PMID: 31999788. DOI: 10.1371/journal.pone.0228582
    OpenUrlCrossRefPubMed
  16. ↵
    1. Khalesi M,
    2. Whiteman DC,
    3. Tran B,
    4. Kimlin MG,
    5. Olsen CM and
    6. Neale RE
    : A meta-analysis of pigmentary characteristics, sun sensitivity, freckling and melanocytic nevi and risk of basal cell carcinoma of the skin. Cancer Epidemiol 37(5): 534-543, 2013. PMID: 23849507. DOI: 10.1016/j.canep.2013.05.008
    OpenUrlCrossRefPubMed
  17. ↵
    1. Williams PF,
    2. Olsen CM,
    3. Hayward NK and
    4. Whiteman DC
    : Melanocortin 1 receptor and risk of cutaneous melanoma: a meta-analysis and estimates of population burden. Int J Cancer 129(7): 1730-1740, 2011. PMID: 21128237. DOI: 10.1002/ijc.25804
    OpenUrlCrossRefPubMed
  18. ↵
    1. Westerdahl J,
    2. Ingvar C,
    3. Mâsbäck A and
    4. Olsson H
    : Sunscreen use and malignant melanoma. Int J Cancer 87(1): 145-150, 2000. PMID: 10861466. DOI: 10.1002/1097-0215(20000701)87:1<145::aid-ijc22>3.0.co;2-3
    OpenUrlCrossRefPubMed
  19. ↵
    1. Green AC,
    2. Baade P,
    3. Coory M,
    4. Aitken JF and
    5. Smithers M
    : Population-based 20-year survival among people diagnosed with thin melanomas in Queensland, Australia. J Clin Oncol 30(13): 1462-1467, 2012. PMID: 22412152. DOI: 10.1200/JCO.2011.38.8561
    OpenUrlAbstract/FREE Full Text
  20. ↵
    1. Rueegg CS,
    2. Stenehjem JS,
    3. Egger M,
    4. Ghiasvand R,
    5. Cho E,
    6. Lund E,
    7. Weiderpass E,
    8. Green AC and
    9. Veierød MB
    : Challenges in assessing the sunscreen-melanoma association. Int J Cancer 144(11): 2651-2668, 2019. PMID: 30447006. DOI: 10.1002/ijc.31997
    OpenUrlCrossRefPubMed
  21. ↵
    1. Lindqvist PG,
    2. Olsson H and
    3. Landin-Olsson M
    : Are active sun exposure habits related to lowering risk of type 2 diabetes mellitus in women, a prospective cohort study? Diabetes Res Clin Pract 90(1): 109-114, 2010. PMID: 20619913. DOI: 10.1016/j.diabres.2010.06.007
    OpenUrlCrossRefPubMed
  22. ↵
    1. Epstein E,
    2. Lindqvist PG,
    3. Geppert B and
    4. Olsson H
    : A population-based cohort study on sun habits and endometrial cancer. Br J Cancer 101(3): 537-540, 2009. PMID: 19550419. DOI: 10.1038/sj.bjc.6605149
    OpenUrlCrossRefPubMed
  23. ↵
    1. Geldenhuys S,
    2. Hart PH,
    3. Endersby R,
    4. Jacoby P,
    5. Feelisch M,
    6. Weller RB,
    7. Matthews V and
    8. Gorman S
    : Ultraviolet radiation suppresses obesity and symptoms of metabolic syndrome independently of vitamin D in mice fed a high-fat diet. Diabetes 63(11): 3759-3769, 2014. PMID: 25342734. DOI: 10.2337/db13-1675
    OpenUrlAbstract/FREE Full Text
  24. ↵
    1. Fleury N,
    2. Feelisch M,
    3. Hart PH,
    4. Weller RB,
    5. Smoothy J,
    6. Matthews VB and
    7. Gorman S
    : Sub-erythemal ultraviolet radiation reduces metabolic dysfunction in already overweight mice. J Endocrinol 233(1): 81-92, 2017. PMID: 28154004. DOI: 10.1530/JOE-16-0616
    OpenUrlAbstract/FREE Full Text
  25. ↵
    1. Ferguson AL,
    2. Kok LF,
    3. Luong JK,
    4. Van Den Bergh M,
    5. Bell- Anderson KS,
    6. Fazakerley DJ and
    7. Byrne SN
    : Exposure to solar ultraviolet radiation limits diet-induced weight gain, increases liver triglycerides and prevents the early signs of cardiovascular disease in mice. Nutr Metab Cardiovasc Dis 29(6): 633-638, 2019. PMID: 30956026. DOI: 10.1016/j.numecd.2019.02.006
    OpenUrlCrossRefPubMed
  26. ↵
    1. Knekt P,
    2. Laaksonen M,
    3. Mattila C,
    4. Härkänen T,
    5. Marniemi J,
    6. Heliövaara M,
    7. Rissanen H,
    8. Montonen J and
    9. Reunanen A
    : Serum vitamin D and subsequent occurrence of type 2 diabetes. Epidemiology 19(5): 666-671, 2008. PMID: 18496468. DOI: 10.1097/EDE.0b013e318176b8ad
    OpenUrlCrossRefPubMed
    1. Triunfo S,
    2. Lanzone A and
    3. Lindqvist PG
    : Low maternal circulating levels of vitamin D as potential determinant in the development of gestational diabetes mellitus. J Endocrinol Invest 40(10): 1049-1059, 2017. PMID: 28555324. DOI: 10.1007/s40618-017-0696-9
    OpenUrlCrossRefPubMed
  27. ↵
    1. Song Y,
    2. Wang L,
    3. Pittas AG,
    4. Del Gobbo LC,
    5. Zhang C,
    6. Manson JE and
    7. Hu FB
    : Blood 25-hydroxy vitamin D levels and incident type 2 diabetes: a meta-analysis of prospective studies. Diabetes Care 36(5): 1422-1428, 2013. PMID: 23613602. DOI: 10.2337/dc12-0962
    OpenUrlAbstract/FREE Full Text
  28. ↵
    1. Pittas AG,
    2. Dawson-Hughes B,
    3. Sheehan P,
    4. Ware JH,
    5. Knowler WC,
    6. Aroda VR,
    7. Brodsky I,
    8. Ceglia L,
    9. Chadha C,
    10. Chatterjee R,
    11. Desouza C,
    12. Dolor R,
    13. Foreyt J,
    14. Fuss P,
    15. Ghazi A,
    16. Hsia DS,
    17. Johnson KC,
    18. Kashyap SR,
    19. Kim S,
    20. LeBlanc ES,
    21. Lewis MR,
    22. Liao E,
    23. Neff LM,
    24. Nelson J,
    25. O’Neil P,
    26. Park J,
    27. Peters A,
    28. Phillips LS,
    29. Pratley R,
    30. Raskin P,
    31. Rasouli N,
    32. Robbins D,
    33. Rosen C,
    34. Vickery EM,
    35. Staten M and D2d Research Group
    : Vitamin D supplementation and prevention of type 2 diabetes. N Engl J Med 381(6): 520-530, 2019. PMID: 31173679. DOI: 10.1056/NEJMoa1900906
    OpenUrlCrossRefPubMed
  29. ↵
    1. Gidlöf S,
    2. Silva AT,
    3. Gustafsson S and
    4. Lindqvist PG
    : Vitamin D and the risk of preeclampsia – a nested case-control study. Acta Obstet Gynecol Scand 94(8): 904-908, 2015. PMID: 25884254. DOI: 10.1111/aogs.12658
    OpenUrlCrossRefPubMed
  30. ↵
    1. Brot C,
    2. Vestergaard P,
    3. Kolthoff N,
    4. Gram J,
    5. Hermann AP and
    6. Sørensen OH
    : Vitamin D status and its adequacy in healthy Danish perimenopausal women: relationships to dietary intake, sun exposure and serum parathyroid hormone. Br J Nutr 86(Suppl 1): S97-103, 2001. PMID: 11520426. DOI: 10.1079/bjn2001345
    OpenUrlCrossRefPubMed
  31. ↵
    1. Wortsman J,
    2. Matsuoka LY,
    3. Chen TC,
    4. Lu Z and
    5. Holick MF
    : Decreased bioavailability of vitamin D in obesity. Am J Clin Nutr 72(3): 690-693, 2000. PMID: 10966885. DOI: 10.1093/ajcn/72.3.690
    OpenUrlAbstract/FREE Full Text
  32. ↵
    1. Vimaleswaran KS,
    2. Berry DJ,
    3. Lu C,
    4. Tikkanen E,
    5. Pilz S,
    6. Hiraki LT,
    7. Cooper JD,
    8. Dastani Z,
    9. Li R,
    10. Houston DK,
    11. Wood AR,
    12. Michaëlsson K,
    13. Vandenput L,
    14. Zgaga L,
    15. Yerges-Armstrong LM,
    16. McCarthy MI,
    17. Dupuis J,
    18. Kaakinen M,
    19. Kleber ME,
    20. Jameson K,
    21. Arden N,
    22. Raitakari O,
    23. Viikari J,
    24. Lohman KK,
    25. Ferrucci L,
    26. Melhus H,
    27. Ingelsson E,
    28. Byberg L,
    29. Lind L,
    30. Lorentzon M,
    31. Salomaa V,
    32. Campbell H,
    33. Dunlop M,
    34. Mitchell BD,
    35. Herzig KH,
    36. Pouta A,
    37. Hartikainen AL, Genetic Investigation of Anthropometric Traits-GIANT Consortium,
    38. Streeten EA,
    39. Theodoratou E,
    40. Jula A,
    41. Wareham NJ,
    42. Ohlsson C,
    43. Frayling TM,
    44. Kritchevsky SB,
    45. Spector TD,
    46. Richards JB,
    47. Lehtimäki T,
    48. Ouwehand WH,
    49. Kraft P,
    50. Cooper C,
    51. März W,
    52. Power C,
    53. Loos RJ,
    54. Wang TJ,
    55. Järvelin MR,
    56. Whittaker JC,
    57. Hingorani AD and
    58. Hyppönen E
    : Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts. PLoS Med 10(2): e1001383, 2013. PMID: 23393431. DOI: 10.1371/journal.pmed.1001383
    OpenUrlCrossRefPubMed
  33. ↵
    1. Wan J,
    2. Yuan J,
    3. Li X,
    4. Bao Y,
    5. Hou Y,
    6. Li Z,
    7. Tan SC,
    8. Low TY and
    9. Chu Y
    : Association between serum vitamin D levels and venous thromboembolism (VTE): A systematic review and meta-analysis of observational studies. Complement Ther Med 54: 102579, 2020. PMID: 33183675. DOI: 10.1016/j.ctim.2020.102579
    OpenUrlCrossRefPubMed
  34. ↵
    1. Blondon M,
    2. Cushman M,
    3. Jenny N,
    4. Michos ED,
    5. Smith NL,
    6. Kestenbaum B and
    7. de Boer IH
    : Associations of serum 25-hydroxyvitamin D with hemostatic and inflammatory biomarkers in the multi-ethnic study of atherosclerosis. J Clin Endocrinol Metab 101(6): 2348-2357, 2016. PMID: 27023449. DOI: 10.1210/jc.2016-1368
    OpenUrlCrossRefPubMed
  35. ↵
    1. Lindqvist PG,
    2. Bremme K,
    3. Hellgren M and Working Group on Hemostatic Disorders (Hem-ARG), Swedish Society of Obstetrics and Gynecology
    : Efficacy of obstetric thromboprophylaxis and long-term risk of recurrence of venous thromboembolism. Acta Obstet Gynecol Scand 90(6): 648-653, 2011. PMID: 21314819. DOI: 10.1111/j.1600-0412.2011.01098.x
    OpenUrlCrossRefPubMed
  36. ↵
    1. Oparil S,
    2. Acelajado MC,
    3. Bakris GL,
    4. Berlowitz DR,
    5. Cífková R,
    6. Dominiczak AF,
    7. Grassi G,
    8. Jordan J,
    9. Poulter NR,
    10. Rodgers A and
    11. Whelton PK
    : Hypertension. Nat Rev Dis Primers 4: 18014, 2018. PMID: 29565029. DOI: 10.1038/nrdp.2018.14
    OpenUrlCrossRefPubMed
  37. ↵
    1. Opländer C,
    2. Volkmar CM,
    3. Paunel-Görgülü A,
    4. van Faassen EE,
    5. Heiss C,
    6. Kelm M,
    7. Halmer D,
    8. Mürtz M,
    9. Pallua N and
    10. Suschek CV
    : Whole body UVA irradiation lowers systemic blood pressure by release of nitric oxide from intracutaneous photolabile nitric oxide derivates. Circ Res 105(10): 1031-1040, 2009. PMID: 19797169. DOI: 10.1161/CIRCRESAHA.109.207019
    OpenUrlAbstract/FREE Full Text
  38. ↵
    1. Liu D,
    2. Fernandez BO,
    3. Hamilton A,
    4. Lang NN,
    5. Gallagher JMC,
    6. Newby DE,
    7. Feelisch M and
    8. Weller RB
    : UVA irradiation of human skin vasodilates arterial vasculature and lowers blood pressure independently of nitric oxide synthase. J Invest Dermatol 134(7): 1839-1846, 2014. PMID: 24445737. DOI: 10.1038/jid.2014.27
    OpenUrlCrossRefPubMed
    1. Muggeridge DJ,
    2. Sculthorpe N,
    3. Grace FM,
    4. Willis G,
    5. Thornhill L,
    6. Weller RB,
    7. James PE and
    8. Easton C
    : Acute whole body UVA irradiation combined with nitrate ingestion enhances time trial performance in trained cyclists. Nitric Oxide 48: 3-9, 2015. PMID: 25289793. DOI: 10.1016/j.niox.2014.09.158
    OpenUrlCrossRefPubMed
    1. Krause R,
    2. Bühring M,
    3. Hopfenmüller W,
    4. Holick MF and
    5. Sharma AM
    : Ultraviolet B and blood pressure. Lancet 352(9129): 709-710, 1998. PMID: 9728997. DOI: 10.1016/S0140-6736(05)60827-6
    OpenUrlCrossRefPubMed
  39. ↵
    1. Scragg R,
    2. Wishart J,
    3. Stewart A,
    4. Ofanoa M,
    5. Kerse N,
    6. Dyall L and
    7. Lawes CM
    : No effect of ultraviolet radiation on blood pressure and other cardiovascular risk factors. J Hypertens 29(9): 1749-1756, 2011. PMID: 21720260. DOI: 10.1097/HJH.0b013e328349666d
    OpenUrlCrossRefPubMed
  40. ↵
    1. Rostand SG,
    2. McClure LA,
    3. Kent ST,
    4. Judd SE and
    5. Gutiérrez OM
    : Associations of blood pressure, sunlight, and vitamin D in community-dwelling adults. J Hypertens 34(9): 1704-1710, 2016. PMID: 27379541. DOI: 10.1097/HJH.0000000000001018
    OpenUrlCrossRefPubMed
  41. ↵
    1. Cabrera SE,
    2. Mindell JS,
    3. Toledo M,
    4. Alvo M and
    5. Ferro CJ
    : Associations of blood pressure with geographical latitude, solar radiation, and ambient temperature: results from the Chilean health survey, 2009-2010. Am J Epidemiol 183(11): 1071-1073, 2016. PMID: 27188937. DOI: 10.1093/aje/kww037
    OpenUrlCrossRefPubMed
  42. ↵
    1. Kent ST,
    2. McClure LA,
    3. Judd SE,
    4. Howard VJ,
    5. Crosson WL,
    6. Al- Hamdan MZ,
    7. Wadley VG,
    8. Peace F and
    9. Kabagambe EK
    : Short-and long-term sunlight radiation and stroke incidence. Ann Neurol 73(1): 32-37, 2013. PMID: 23225379. DOI: 10.1002/ana.23737
    OpenUrlCrossRefPubMed
  43. ↵
    1. Ke L,
    2. Ho J,
    3. Feng J,
    4. Mpofu E,
    5. Dibley MJ,
    6. Feng X,
    7. Van F,
    8. Leong S,
    9. Lau W,
    10. Lueng P,
    11. Kowk C,
    12. Li Y,
    13. Mason RS and
    14. Brock KE
    : Modifiable risk factors including sunlight exposure and fish consumption are associated with risk of hypertension in a large representative population from Macau. J Steroid Biochem Mol Biol 144 Pt A: 152-155, 2014. PMID: 24189545. DOI: 10.1016/j.jsbmb.2013.10.019
    OpenUrlCrossRefPubMed
  44. ↵
    1. Al-Daghri NM,
    2. Alkharfy KM,
    3. Al-Saleh Y,
    4. Al-Attas OS,
    5. Alokail MS,
    6. Al-Othman A,
    7. Moharram O,
    8. El-Kholie E,
    9. Sabico S,
    10. Kumar S and
    11. Chrousos GP
    : Modest reversal of metabolic syndrome manifestations with vitamin D status correction: a 12-month prospective study. Metabolism 61(5): 661-666, 2012. PMID: 22075268. DOI: 10.1016/j.metabol.2011.09.017
    OpenUrlCrossRefPubMed
  45. ↵
    1. Weller RB,
    2. Wang Y,
    3. He J,
    4. Maddux FW,
    5. Usvyat L,
    6. Zhang H,
    7. Feelisch M and
    8. Kotanko P
    : Does incident solar ultraviolet radiation lower blood pressure? J Am Heart Assoc 9(5): e013837, 2020. PMID: 32106744. DOI: 10.1161/JAHA.119.013837
    OpenUrlCrossRefPubMed
  46. ↵
    1. Wang L,
    2. Song Y,
    3. Manson JE,
    4. Pilz S,
    5. März W,
    6. Michaëlsson K,
    7. Lundqvist A,
    8. Jassal SK,
    9. Barrett-Connor E,
    10. Zhang C,
    11. Eaton CB,
    12. May HT,
    13. Anderson JL and
    14. Sesso HD
    : Circulating 25-hydroxy-vitamin D and risk of cardiovascular disease: a meta-analysis of prospective studies. Circ Cardiovasc Qual Outcomes 5(6): 819-829, 2012. PMID: 23149428. DOI: 10.1161/CIRCOUTCOMES.112.967604
    OpenUrlAbstract/FREE Full Text
  47. ↵
    1. Lindqvist PG,
    2. Landin-Olsson M and
    3. Olsson H
    : Low sun exposure habits is associated with a dose-dependent increased risk of hypertension: a report from the large MISS cohort. Photochem Photobiol Sci 20(2): 285-292, 2021. PMID: 33721253. DOI: 10.1007/s43630-021-00017-x
    OpenUrlCrossRefPubMed
  48. ↵
    1. Faeh D,
    2. Gutzwiller F,
    3. Bopp M and Swiss National Cohort Study Group
    : Lower mortality from coronary heart disease and stroke at higher altitudes in Switzerland. Circulation 120(6): 495-501, 2009. PMID: 19635973. DOI: 10.1161/CIRCULATIONAHA.108.819250
    OpenUrlAbstract/FREE Full Text
  49. ↵
    1. Yang L,
    2. Lof M,
    3. Veierød MB,
    4. Sandin S,
    5. Adami HO and
    6. Weiderpass E
    : Ultraviolet exposure and mortality among women in Sweden. Cancer Epidemiol Biomarkers Prev 20(4): 683-690, 2011. PMID: 21297041. DOI: 10.1158/1055-9965.EPI-10-0982
    OpenUrlAbstract/FREE Full Text
PreviousNext
Back to top

In this issue

Anticancer Research: 42 (4)
Anticancer Research
Vol. 42, Issue 4
April 2022
  • Table of Contents
  • Table of Contents (PDF)
  • Index by author
  • Back Matter (PDF)
  • Ed Board (PDF)
  • Front Matter (PDF)
Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word on Anticancer Research.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Sun Exposure - Hazards and Benefits
(Your Name) has sent you a message from Anticancer Research
(Your Name) thought you would like to see the Anticancer Research web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
14 + 5 =
Solve this simple math problem and enter the result. E.g. for 1+3, enter 4.
Citation Tools
Sun Exposure - Hazards and Benefits
PELLE G. LINDQVIST, ELISABETH EPSTEIN, MONA LANDIN-OLSSON
Anticancer Research Apr 2022, 42 (4) 1671-1677; DOI: 10.21873/anticanres.15644

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Reprints and Permissions
Share
Sun Exposure - Hazards and Benefits
PELLE G. LINDQVIST, ELISABETH EPSTEIN, MONA LANDIN-OLSSON
Anticancer Research Apr 2022, 42 (4) 1671-1677; DOI: 10.21873/anticanres.15644
Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • MISS Cohort
    • Skin Cancer and Cancer Mortality
    • Redheads or Fair Skin
    • Sunscreen Use
    • Type 2 Diabetes Mellitus (T2DM)
    • Cardiovascular Disease (CVD) and CVD Mortality
    • All-cause Mortality and Sun Exposure
    • Conclusion
    • Footnotes
    • References
  • Info & Metrics
  • PDF

Related Articles

  • No related articles found.
  • PubMed
  • Google Scholar

Cited By...

  • Regional variation of cancer incidence in Panama
  • Improved Vitamin D Status Is Associated With Lower Incidence of Stillbirth
  • Google Scholar

More in this TOC Section

  • Immunotherapy and Chemotherapy for Advanced or Recurrent Endometrial Carcinoma
  • Cancer Stem Cells in Glioblastoma: The Role of the mTOR Pathway
  • Cannabinoids as Potential Therapeutic Agents in the Treatment of Pancreatic Cancer
Show more Review

Similar Articles

Keywords

  • UV exposure
  • diabetes mellitus
  • cancer
  • Melanoma
  • cardiovascular disease
  • mortality
  • review
Anticancer Research

© 2025 Anticancer Research

Powered by HighWire