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Research ArticleClinical Studies

Increase in Circulating Tumor Cells in Invasive Bladder Cancer After Transurethral Resection of Bladder Tumor

NOBUHIRO HAGA, KAZUNA TSUBOUCHI, HIROKO MARUTA, TOMOYUKI KOGUCHI, SEIJI HOSHI, SOICHIRO OGAWA, HIDENORI AKAIHATA, JUNYA HATA and YOSHIYUKI KOJIMA
Anticancer Research August 2020, 40 (8) 4299-4307; DOI: https://doi.org/10.21873/anticanres.14432
NOBUHIRO HAGA
1Department of Urology, Fukushima Medical University School of Medicine, Fukushima, Japan
2Department of Urology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan
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  • For correspondence: nhaga{at}fukuoka-u.ac.jp
KAZUNA TSUBOUCHI
2Department of Urology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan
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HIROKO MARUTA
2Department of Urology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan
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TOMOYUKI KOGUCHI
1Department of Urology, Fukushima Medical University School of Medicine, Fukushima, Japan
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SEIJI HOSHI
1Department of Urology, Fukushima Medical University School of Medicine, Fukushima, Japan
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SOICHIRO OGAWA
1Department of Urology, Fukushima Medical University School of Medicine, Fukushima, Japan
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HIDENORI AKAIHATA
1Department of Urology, Fukushima Medical University School of Medicine, Fukushima, Japan
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JUNYA HATA
1Department of Urology, Fukushima Medical University School of Medicine, Fukushima, Japan
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YOSHIYUKI KOJIMA
1Department of Urology, Fukushima Medical University School of Medicine, Fukushima, Japan
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    Figure 1.

    Typical multi-parametric magnetic resonance imaging in non-muscle invasive bladder cancer. A: Axial T2-weighted image shows a 1.3-cm exophytic tumor, with a sessile/broad-based tumor and a high-signal-intensity, thickened inner layer. B: Dynamic contrast-enhanced image shows early enhancement of the inner layer without early enhancement of muscularis propria. C: Diffusion-weighted image showing high-signal-intensity tumor and muscularis propria with intermediate continuous signal intensity. D: Apparent diffusion coefficient map showing a hypointense tumor. These figures suggest that a Vesical Imaging-Reporting and Data System Score of 1, which was composed of a T2-weighted imaging score of 1, dynamic contrast-enhanced imaging score of 1, and diffusion-weighted imaging score of 1, can be obtained. White and black arrows indicate the bladder tumor.

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    Figure 2.

    Typical multi-parametric magnetic resonance imaging in muscle-invasive bladder cancer. A: T2-Weighted image showing extension of intermediate signal intensity tumor to extravesical fat, representing invasion of the entire bladder wall. B: Dynamic contrast-enhanced image showing tumor with early enhancement that extended to the entire bladder wall and to extravesical fat. C: Diffusion-weighted image showing high-signal-intensity tumor that extends to the entire bladder wall and to extravesical fat. D: Apparent diffusion coefficient map showinq low-signal-intensity tumor that extends to the entire bladder wall and to extravesical fat. These figures suggest that a Vesical Imaging-Reporting and Data System Score of 5, which was composed of a T2-weighted imaging score of 5, dynamic contrast-enhanced imaging score of 5, and diffusion-weighted imaging score of 5, can be obtained. White and black arrows indicate the bladder tumor.

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    Figure 3.

    Flow cytometric detection of circulating tumor cells (CTCs) by the FISHMAN-R. CTCs are defined as cell nuclei-positive, cytokeratin (CK)-positive, epithelial cell adhesion molecule (EpCAM)-positive, and CD45-negative. After cells were detected by both forward scattered light (FSC) and side scattered light (SSC) (A), cell nuclei-positive cells were confirmed using 4’,6-diamidino-2-phenylindole (DAPI) (cell nucleus) (B). Both EpCAM-positive and CK-positive CTCs were identified using phycoerythrin (PE) against fluorescein isothiocyanate (FITC) density plots (C). EpCAM-positive cells were distinguished as CD45-negative using PE-Cy7 against PE density plots (D). CK-positive cells were distinguished as CD45-negative using PE-Cy7 against FITC density plots (E). Finally, the number of CTCs evaluated by FISHMAN-R was calculated using FlowJo software (F).

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    Figure 4.

    Comparison of the number of circulating tumor cells (CTCs) between non-muscle-invasive (NMIBC) and muscle-invasive (MIBC) bladder cancer. A: Number of preoperative CTCs. B: Number of postoperative CTCs. C: Perioperative change in CTCs. Lines indicate the median, boxes indicate the interquartile range, and bars indicate the minimum and maximum. *Significantly different at p<0.05.

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    Figure 5.

    Correlation of the volume of irrigation fluid used during transurethral resection of bladder tumor with the number of CTCs postoperatively (A) and change in the number of CTCs (postoperative–preoperative) (B).

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    Figure 6.

    Correlation of the duration of surgery with the number of circulating tumor cells (CTCs) postoperatively (A) and change in the number of CTCs (postoperative–preoperative).

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Increase in Circulating Tumor Cells in Invasive Bladder Cancer After Transurethral Resection of Bladder Tumor
NOBUHIRO HAGA, KAZUNA TSUBOUCHI, HIROKO MARUTA, TOMOYUKI KOGUCHI, SEIJI HOSHI, SOICHIRO OGAWA, HIDENORI AKAIHATA, JUNYA HATA, YOSHIYUKI KOJIMA
Anticancer Research Aug 2020, 40 (8) 4299-4307; DOI: 10.21873/anticanres.14432

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Increase in Circulating Tumor Cells in Invasive Bladder Cancer After Transurethral Resection of Bladder Tumor
NOBUHIRO HAGA, KAZUNA TSUBOUCHI, HIROKO MARUTA, TOMOYUKI KOGUCHI, SEIJI HOSHI, SOICHIRO OGAWA, HIDENORI AKAIHATA, JUNYA HATA, YOSHIYUKI KOJIMA
Anticancer Research Aug 2020, 40 (8) 4299-4307; DOI: 10.21873/anticanres.14432
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Keywords

  • circulating tumor cells
  • Bladder cancer
  • transurethral resection of bladder tumor
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