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
Research ArticleExperimental Studies

Enhancement of Sodium Butyrate-induced Cell Death by Hyperthermia in HCT 116 Human Colorectal Cancer Cells

ZHENG-LI WEI, QING-LI ZHAO, DA-YONG YU, MARIAME A. HASSAN and TAKASHI KONDO
Anticancer Research May 2008, 28 (3A) 1693-1700;
ZHENG-LI WEI
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
QING-LI ZHAO
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DA-YONG YU
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
MARIAME A. HASSAN
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
TAKASHI KONDO
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: kondot@med.u-toyama.ac.jp
  • Article
  • Info & Metrics
  • PDF
Loading

Abstract

Aim: The possible enhancing effect of the combined use of sodium butyrate (SB) and hyperthermia to kill HCT 116 cells was evaluated. Materials and Methods: HCT 116 cells were subjected to SB (1 mM) treatment followed by hyperthermia (44°C 60 min) and the effects on cell death, cell proliferation and the cell cycle were examined. Apoptosis-indicating protein expressions and intracellular superoxide formation were also analysed. Results: A marked reduction in the growth rate of the combined-treatment group was observed compared to those of the single-treatment groups. This involved the increased expression of p53 and p21, the alteration of the balance of anti- and proapoptotic Bcl-2 family proteins and enhanced superoxide formation. However, the death receptor pathway played no role. Conclusion: Hyperthermia synergistically promoted cell death induced by SB. Thus, the combined treatment led to mutual potentiation of the killing effects of each agent.

  • Sodium butyrate
  • hyperthermia
  • cell death
  • apoptosis
  • HCT 116 colorectal cancer cells

Footnotes

  • Received January 11, 2008.
  • Revision received March 21, 2008.
  • Accepted March 27, 2008.
  • Copyright© 2008 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved
PreviousNext
Back to top

In this issue

Anticancer Research: 28 (3A)
Anticancer Research
Vol. 28, Issue 3A
May-June 2008
  • Table of Contents
  • Table of Contents (PDF)
  • Index by author
  • Front Matter (PDF)
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.
Enhancement of Sodium Butyrate-induced Cell Death by Hyperthermia in HCT 116 Human Colorectal Cancer Cells
(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.
3 + 1 =
Solve this simple math problem and enter the result. E.g. for 1+3, enter 4.
Citation Tools
Enhancement of Sodium Butyrate-induced Cell Death by Hyperthermia in HCT 116 Human Colorectal Cancer Cells
ZHENG-LI WEI, QING-LI ZHAO, DA-YONG YU, MARIAME A. HASSAN, TAKASHI KONDO
Anticancer Research May 2008, 28 (3A) 1693-1700;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Reprints and Permissions
Share
Enhancement of Sodium Butyrate-induced Cell Death by Hyperthermia in HCT 116 Human Colorectal Cancer Cells
ZHENG-LI WEI, QING-LI ZHAO, DA-YONG YU, MARIAME A. HASSAN, TAKASHI KONDO
Anticancer Research May 2008, 28 (3A) 1693-1700;
Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
  • Info & Metrics
  • PDF

Related Articles

  • No related articles found.
  • PubMed
  • Google Scholar

Cited By...

  • No citing articles found.
  • Google Scholar

More in this TOC Section

  • CA9-Positive Keloid Fibroblasts: Modulator of Local Inflammation Induced by the Hypoxic and Glycolysis-enhanced Microenvironment
  • Predictive Factors for Multiple Metastases of Clear-cell Renal Cell Carcinoma
  • Acyclic Retinoid Overcomes Vemurafenib Resistance in Melanoma Cells via Dual Inhibition of MAPK and PI3K/AKT/mTOR Pathways
Show more Experimental Studies

Similar Articles

Anticancer Research

© 2025 Anticancer Research

Powered by HighWire