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癌症干细胞标志物OCT4和CD133在移行细胞癌中的表达

Expression of Cancer Stem Cell Markers OCT4 and CD133 in Transitional Cell Carcinomas.

作者信息

Sedaghat Shirin, Gheytanchi Elmira, Asgari Mojgan, Roudi Raheleh, Keymoosi Hossein, Madjd Zahra

机构信息

*Oncopatholgy Research Center †Department of Pathology ‡Department of Pathology, Hasheminejad Urology-Nephrology Center §Department of Molecular Medicine, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.

出版信息

Appl Immunohistochem Mol Morphol. 2017 Mar;25(3):196-202. doi: 10.1097/PAI.0000000000000291.

Abstract

BACKGROUND

Treatment failure, recurrence, and metastasis in bladder cancer are attributed to a subset of tumor cells expressing cancer stem cell (CSC) markers. This study aimed to explore the expression levels and the clinical significance of putative CSC markers OCT4 and CD133 in bladder cancer.

MATERIALS AND METHODS

Tissue microarray-based immunohistochemical analysis was applied to investigate the expression patterns of potential CSC markers OCT4 and CD133 in bladder cancer samples. The correlation between the expressions of each marker and clinicopathologic parameters was then analyzed.

RESULTS

There was a significant association between OCT4 expression and the TNM stage of bladder cancer (P<0.001). Our analysis demonstrated a significant association between the intensity of staining and the presence of lamina propria and muscularis propria invasion (P=0.02 and 0.02, respectively), whereas a relative inverse correlation was found between CD133 expression with lamina propria invasion (P=0.051) and muscularis propria invasion (P=0.07).

CONCLUSIONS

The correlation of OCT4, but not CD133, with the invasiveness of bladder cancer revealed that OCT4 can be considered as a key regulator of tumor progression, aggressive behavior, and metastasis; therefore, OCT4 can be a potential marker for targeted therapy of bladder cancer.

摘要

背景

膀胱癌的治疗失败、复发和转移归因于表达癌症干细胞(CSC)标志物的肿瘤细胞亚群。本研究旨在探讨假定的CSC标志物OCT4和CD133在膀胱癌中的表达水平及其临床意义。

材料与方法

应用基于组织芯片的免疫组化分析来研究潜在的CSC标志物OCT4和CD133在膀胱癌样本中的表达模式。然后分析每个标志物的表达与临床病理参数之间的相关性。

结果

OCT4表达与膀胱癌的TNM分期之间存在显著关联(P<0.001)。我们的分析表明,染色强度与固有层和肌层浸润的存在之间存在显著关联(分别为P=0.02和0.02),而CD133表达与固有层浸润(P=0.051)和肌层浸润(P=0.07)之间存在相对负相关。

结论

OCT4而非CD133与膀胱癌侵袭性的相关性表明,OCT4可被视为肿瘤进展、侵袭行为和转移的关键调节因子;因此,OCT4可作为膀胱癌靶向治疗的潜在标志物。

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