期刊文献+

CD44^+/CD24^+表型的宫颈癌Siha细胞对顺铂的耐药及机制研究 被引量:2

Study on the chemoresistance of CD44^+/CD24^+ Siha cells to cisplatin and its mechanisms
在线阅读 下载PDF
导出
摘要 背景与目的:肿瘤干细胞的存在是肿瘤细胞抗拒化疗的原因之一。该研究探讨CD44+/CD24+宫颈癌Siha细胞对顺铂的耐药性及相关机制。方法:体外培养Siha细胞,流式荧光激活细胞分选仪分选CD44+/CD24+Siha细胞,噻唑蓝(thiazolyl blue,MTT)法检测不同浓度顺铂对细胞的体外抑制情况,采用流式细胞仪检测10μg/m L顺铂作用于CD44+/CD24+Siha细胞24、48和72 h时的细胞凋亡率,实时定量聚合酶链式反应(quantitutive real-time polymerase chain reaction,q RT-PCR)和蛋白[质]印迹法(Western blot)检测CD44+/CD24+Siha细胞中Oct-4、ABCG2、Bcl-2的表达,同时设立亲代Siha细胞作为对照。结果:不同浓度顺铂(0.1、1、5、10、15和20μg/m L)对CD44+/CD24+Siha细胞的增殖抑制作用较亲代Siha细胞小[(88.4±1.5)%vs(92.9±1.5)%,(79.9±1.0)%vs(84.7±1.1)%,(69.8±0.8)%vs(75.1±2.9)%,(59.0±0.7)%vs(65.8±2.7)%,(49.6±0.9)%vs(52.1±0.5)%,(45.1±0.7)%vs(48.8±1.0)%,P<0.05];与亲代细胞相比,当10μg/m L顺铂作用于CD44+/CD24+Siha细胞时,发现在24、48和72 h时的细胞凋亡率均较小[(3.05±0.16)%vs(5.17±0.27)%,(17.94±2.02)%vs(32.60±4.28)%和(40.14±3.01)%vs(56.62±5.32)%,P<0.05]。q RT-PCR和Western blot实验均显示CD44+/CD24+Siha细胞高表达Oct-4、ABCG2和Bcl-2,与亲代Siha细胞比较差异有统计学意义(P=0.015)。结论:CD44+/CD24+Siha细胞可以抵抗顺铂诱导的细胞凋亡,具有化疗抵抗性,并且高表达肿瘤干细胞表面标志物如Oct-4和ABCG2,该结果在宫颈癌肿瘤干细胞的有效分选以及肿瘤靶向治疗方面有深远意义。 Background and purpose:One of the reasons why cancer cells are resistant to chemotherapy is the existence of cancer stem cells. The purpose of this study was to investigate the chemoresistance of CD44+/CD24+ Siha cells to cisplatin and its mechanisms.Methods:Siha cells were cultivatedin vitro. The CD44+/CD24+ Siha cells were sorted out by fluorescence activated cell sorter (FACS) andin vitro proliferation was detected by MTT assay after treatment with the different concentrations of cisplatin. The cell apoptosis rate was detected by flow cytometry after 10 μg/mL cisplatin acted on CD44+/CD24+ Siha cells for 24, 48 and 72 h. The relative mRNA and protein expressions of Bcl-2, Oct-4 and ABCG2 were detected by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot, respectively. Results:The survival rates of CD44+/CD24+ Siha cells treated with different concentrations of cisplatin (0.1, 1, 5, 10, 15 and 20 μg/mL) were higher than those of their parental Siha cells [(88.42±1.51)%vs (92.87±1.5)%, (79.94±1.05)%vs (84.72±1.09)%, (69.78±0.81)%vs (75.13±2.86)%, (58.97±0.70)%vs (65.79±2.71)%, (49.60±0.88)%vs (52.10±0.52)%, (45.13±0.69)%vs (48.84±1.02)%,P〈0.05]. Compared with their parental Siha cells, the apoptosis rates of CD44+/CD24+ Siha cells were lower after 10 μg/mL of cisplatin acting on them for 24, 48 and 72 h, respectively [(3.05±0.16)%vs (5.17±0.27)%, (17.94±2.02)%vs (32.60±4.28)% and (40.14±3.01)%vs (56.62±5.32)%,P〈0.05]. The results from both qRT-PCR and Western blot indicated that Oct-4, ABCG2 and Bcl-2 were highly expressed on CD44+/CD24+ Siha cells. A significant difference was found in Oct-4, ABCG2 and Bcl-2 expression between CD44+/CD24+Siha cells and their parental cells (P=0.015〈0.05).Conclusion:CD44+/CD24+ Siha cells could be resistant to apoptosis induced by cisplatin and expressed high levels of cancer stem cell markers such as Oct-4 and ABCG2. This study lays the basis for useful isolation and further targeted therapy of cervical cancer stem cells.
出处 《中国癌症杂志》 CAS CSCD 北大核心 2015年第10期785-790,共6页 China Oncology
基金 河北省科技支撑计划(14277770D) 河北省杰出青年科学基金(C2010002011)
关键词 宫颈癌 肿瘤干细胞 CD44+ CD24+ 顺铂 耐药 凋亡 Cervical cancer Cancer stem cells Cisplatin Drug resistance Apoptosis
  • 相关文献

参考文献14

二级参考文献150

共引文献155

同被引文献45

  • 1张伟.生物荧光肿瘤体外药敏检测技术的临床应用及其探讨[J].癌症进展,2005,3(5):427-435. 被引量:12
  • 2吕讷男,孔为民.宫颈癌耐药基因的表达及其与同步放化疗疗效的关系[J].肿瘤学杂志,2006,12(5):385-388. 被引量:8
  • 3Bourguignon LY, Peyrollier K, Xia W, et al. Hyaluronan-CD44 interaction activates stem cell marker Nanog, Stat-3-mediated MDR1 gene expression, and ankyrin-regulated multidrug efflux in breast and ovarian tumor cells. J Biol Chem. 2008; 283(25): 17635-17651.
  • 4Yang J, Lam DH, Goh SS, et al. Tumor tropism of intravenously injected human-induced pluripotent stem cell-derived neural stem cells and their gene therapy application in a metastatic breast cancer model. Stem Cells. 2012;30(5): 1021-1029.
  • 5DevapaUa B, Sanders J, Samuelson DJ. Genetically determined inflammatory-response related cytokine and chemokine transcript profiles between mammary carcinoma resistant and susceptible rat strains. Cytokine. 2012;59(2):223-227.
  • 6Lee Y J, Galoforo SS, Berns CM, et al. Glucose deprivation-induced cytotoxicity and alterations in mitogen-activated protein kinase activation are mediated by oxidative stress in multidrug-resistant human breast carcinoma cells. J Biol Chem. 1998; 273(9):5294-5299.
  • 7Manuvakhova M, Thottassery JV, Hays S, et al. Expression of the SNT-1/FRS2 phosphotyrosine binding domain inhibits activation of MAP kinase and PI3-kinase pathways and antiestrogen resistant growth induced by FGF-1 in human breast carcinoma cells. Oncogene. 2006;25(44):6003-6014.
  • 8Ferguson P J, Brisson AR, Koropatnick J, et al. Enhancement of cytotoxicity of natural product drugs against multidrug resistant variant cell lines of human head and neck squamous cell carcinoma and breast carcinoma by tesmilifene. Cancer Lett. 2009; 274(2): 279-289.
  • 9Lee SA, Jung M. The nucleoside analog sangivamycin induces apoptotic cell death in breast carcinoma MCF7/adriamycin-resistant cells via protein kinase Cdelta and JNK activation. J Biol Chem. 2007; 282(20) 15271- 15783.
  • 10Heimberger AB, Sampson JH. The PEPvlII-KLH (CDX-110) vaccine in glioblastoma multiforme patients. Expert Opin Biol Ther. 2009;9(8): 1087-1098.

引证文献2

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部