| 赵乐 纪新强 刘静 武加利 张文卿.Nanog 基因在卵巢癌和卵巢肿瘤干细胞中的表达及意义[J].现代生物医学进展英文版,2012,12(14):2642-2646. |
| Nanog 基因在卵巢癌和卵巢肿瘤干细胞中的表达及意义 |
| Expression and Significance of Nanog Gene in Ovarian Cancerand Ovarian Cancer Stem Cells |
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| DOI： |
| 中文关键词: 卵巢癌 Nanog 肿瘤干细胞 基因表达 悬浮培养 |
| 英文关键词: Ovarian cancer Nanog Cancer stem cell Gene expression Floating culture system |
| 基金项目:山东省自然科学基金(Y2008c33) |
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| 中文摘要: |
| 目的：探讨胚胎干细胞关键因子Nanog 基因mRNA 及其蛋白在卵巢癌和卵巢癌肿瘤干细胞中的表达及意义。方法：选取10
例正常卵巢上皮组织、10 例卵巢良性肿瘤及60 例卵巢癌组织，采用逆转录酶- 聚合酶链反应(RT-PCR) 方法和免疫组织化学
PV-6000 两步法检测Nanog mRNA 和蛋白表达水平；采用无血清悬浮培养法从SKOV-3 卵巢癌细胞株中分离培养肿瘤干细胞，
流式细胞术鉴定肿瘤干细胞CD117 表达，采用RT-PCR 和Western Blot 方法检测SKOV-3 卵巢癌细胞及肿瘤干细胞中Nanog
mRNA 及其蛋白的表达水平。结果：Nanog mRNA 在卵巢癌组织中的表达水平均高于正常卵巢组织和卵巢良性肿瘤组织(P<0.
05)；Nanog mRNA 在不同分化程度及临床分期的卵巢癌组织中表达水平不同，低分化组高于高分化组(P<0.05)；III-IV 期高于I-II
期(P<0.05)；免疫组化结果同RT-PCR。从SKOV-3 卵巢癌细胞株中成功分离出肿瘤干细胞，SKOV-3 卵巢癌细胞和肿瘤干细胞
Nanog mRNA 相对含量分别为0.6044±0.0368,0.8736±0.0537，差异具有统计学意义(P<0.05)，两种细胞Nanog 蛋白相对含量分
别为0.6364±0.0169 1.2788±0.0314，差别具有统计学意义(P<0.05)。结论：Nanog 基因在卵巢癌组织和SKOV-3 细胞系中均高表
达，其在组织中的表达强度与临床分期及病理分级关系密切，且在肿瘤干细胞中表达高于一般卵巢癌细胞，其与卵巢癌的发生发
展关系密切，可能是卵巢癌干细胞的表面标志物,有望成为新的标志物。 |
| 英文摘要: |
| Objective: To explore the expression of embryonic stem cells key transcription factor Nanog mRNA and protein in
ovarian cancer and cancer stem cells. Methods: Reverse transcription polymerase chain reaction (RT-PCR) and immunohistochemistry
were performed to detect the expression of Nanog gene in 10 cases of normal ovaries,10 cases of benign ovarian tumors and 60 cases of
ovarian cancer. Ovarian caner stem cells were isolated from ovarian cell line SKOV-3 and cultured in serum free medium by nanosphere
suspension. Flow cytometry analysis was used to examine the expression of the cell surface marker CD117 in SKOV-3 and ovarian cancer
stem cells. We examined the expression of Nanog gene in SKOV-3 and ovarian cancer stem cells by RT-PCR and Western Blot. Results:
Nanog gene expression in ovarian cancer was significantly higher than in normal ovarian tissue and benign ovarian tumors (P<0.05). The
Nanog expression was higher in ovarian cancer with poorly differentiated grade or advanced stage than well differentiated or early stage,
respectively (P<0.05). Ovarian caner stem cells were isolated, the relative level of Nanog mRNA was 0.6044±0.0368 in SKOV-3 and
0.8736±0.0537 in ovarian tumor stem cell (P<0.05). The relative level of Nanog protein was 0.6364±0.0169 in SKOV-3, and 1.2788±
0.0314 in ovarian tumor stem cell (P<0.05). Conclusions: Nanog gene is highly expressed in ovarian cancer and SKOV-3, which is
associated with the differentiation and clinic stage. And Nanog gene is more highly expressed in ovarian cancer stem cell than SKOV-3,
which is associated with the development and progression of ovarian cancer. Nanog maybe the antigen marker of ovarian cancer stem
cells and could be as novel marker for ovarian cancer. |
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