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PTEN/β-catenin/Nanog在鼻咽癌组织干细胞中表达相关性的研究

ZHU Wenting ZHANG Gong LI Xiaonan DING Rui REN Jinjin

肿瘤药学2019,Vol.9Issue(2):204-207,218,5.
肿瘤药学2019,Vol.9Issue(2):204-207,218,5.DOI:10.3969/j.issn.2095-1264.2019.02.06

PTEN/β-catenin/Nanog在鼻咽癌组织干细胞中表达相关性的研究

Research on the Expression Correlation of PTEN, β-catenin and Nanog in Nasopharygeal Cancer Stem Cell

ZHU Wenting 1ZHANG Gong 2LI Xiaonan 2DING Rui 1REN Jinjin2

作者信息

  • 1. Shanxi Medical University, Taiyuan, Shanxi, 030001, China
  • 2. Department of Radiotherapy of People’s Hospital Affiliated to Shanxi Medical University, Taiyuan, Shanxi, 030012, China
  • 折叠

摘要

Abstract

Objective PTEN has been suggested to play a role in radiotherapy of head and neck tumors. β-catenin is involved in regu-lating cancer stem cells. Nanog is one of the cancer stem cells markers. This study aims to explore the correlation of the mentioned three proteins in nasopharyngeal carcinoma (NPC) tissue stem cells by testing the expression of PTEN, β-catenin and Nanog. Methods Immuno-histochemistry was used to detect the differential expression of PTEN, β-catenin (cyteblast) and Nanog (cyteblast) on a tumor issue microar-ray consisting of paraffin-embedded NPC samples derived from 130 patients. Results Negative immunostaining for PTEN was found in 62 of 130 tumors (48%).Thirty-eight (61%) out of the sixty-two specimens with negative PTEN staining displayed both nucleus β-catenin and Nanog immunoreactivity. Negative expression of PTEN in NPC was significantly associated with nuclear expression of β-catenin and Nanog. The nuclear expression of β-catenin was positively correlated with the Nanog. Conclusion The PTEN/β-catenin/Nanog axis is involved in the regulation of cancer stem cells in NPC.

关键词

鼻咽癌/肿瘤干细胞/PTEN/β-catenin/Nanog

Key words

Nasopharyngeal carcinoma/Cancer stem cells/PTEN/β-catenin/Nanog

分类

医药卫生

引用本文复制引用

ZHU Wenting,ZHANG Gong,LI Xiaonan,DING Rui,REN Jinjin..PTEN/β-catenin/Nanog在鼻咽癌组织干细胞中表达相关性的研究[J].肿瘤药学,2019,9(2):204-207,218,5.

基金项目

国家自然科学基金(NO.81402458). (NO.81402458)

肿瘤药学

OACSTPCD

2095-1264

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