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STAT3特异性抑制剂STA-21对乳腺癌MCF-7B细胞增殖及凋亡的影响

Effects of specific inhibitor of STAT3:STA-21 on the proliferation and apoptosis of breast cancer MCF-7B cells
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摘要 目的:探讨信号传导与转录活化因子3(signal transducers and activators of transcription 3,STAT3)特异性抑制剂STA-21对乳腺癌MCF-7B细胞增殖及凋亡的影响。方法:空白组为单独培养MCF-7B细胞,实验组采用不同浓度STA-21作用于乳腺癌MCF-7B细胞后,用MTT法观察STA-21对MCF-7B细胞生长抑制的作用;流式细胞仪检测细胞周期及凋亡;Westernblot检测MCF-7B细胞P-STAT3、STAT3、细胞周期蛋白D1(CyclinD1)、Bcl-xl蛋白的表达。结果:MCF-7B细胞经各浓度STA-21(10、30、50μmol/L)作用后,其细胞增殖的抑制率及细胞凋亡率较空白组明显增加(P=0.000);流式细胞仪检测发现STA-21可导致MCF-7B细胞阻滞于G1期;Western blot结果显示与空白组相比,STA-21可降低MCF-7B细胞P-STAT3、CyclinD1、Bcl-xl蛋白的表达(P=0.000),但对STAT3蛋白的表达基本无影响(P=0.367)。结论:STA-21可在一定程度上抑制MCF-7B细胞的增殖及促进凋亡,其作用机制可能与抑制STAT3活性有关。 Objective:To investigate the effects of STA-21,a specific inhibitor of signal transducers and activators of transcription 3 (STAT3) on the proliferation and apoptosis of breast cancer MCF-7B cells. Methods :MTY assay was applied to observe the inhibi- tion of STA-21 on growth of MCF-7B cells after MCF-7B cells being treated with different concentrations of STA-21. Apoptosis and cell cycle of MCF-7B cells were examined by flow cytometry(FCM). Expressions of P-STAT3, STAT3, CyclinD1 and Bcl-xl protein in MCF-7B cells were detected by Western blot. Results:After cells being exposed to different concentrations ( 10,30,50 ~mol/L)of STA-21, inhibitory rate and apoptotic rate were increased markedly(P=0.000). It was showed by FCM assay that STA-21 could inhibit the MCF-7B cells at G1 phase. Meanwhile,STA-21 could reduce the expressions of P-STAT3, CyclinD1 and Bcl-xl protein(P=0.000), but STA-21 exerted no effect on STAT3 protein(P=0.367). Conclusions:Our study demonstrates that STA-21 can inhibit prolifer- ation and promote apoptosis of MCF-TB, mechanism of which may be related with the inhibition of STAT3 activity.
出处 《重庆医科大学学报》 CAS CSCD 北大核心 2013年第5期469-473,共5页 Journal of Chongqing Medical University
基金 国家自然科学基金资助项目(编号:31140035) 重庆市自然科学基金资助项目(编号:cstc2011jjA10060)
关键词 MCF-7B细胞 信号传导与转录活化因子3 STA-21 抑制 MCF-7B cells signal transducers and activators of transcription 3 STA-21 inhibition
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  • 1徐兵河.乳腺癌临床研究的进展与未来[J].中华肿瘤杂志,2007,29(12):881-883. 被引量:12
  • 2Ptonka J,Latocha M.Photodynamic therapy in the treatment of breast cancer[J].Pol Merkur Lekarski, 2012,33 (195) : 173-175.
  • 3Behera R,Kumar V,Lohite K, et al.Activation of JAK2/STAT3 sig- naling by osteopontin promotes tumor growth in human breast cancer eells[J].Careinogenesis, 2010,31 (2) : 192-200.
  • 4Zhao X,Sun X,Li X L.Expression and clinical significance of STAT3,P-STAT3 and VEGF-C in small cell lung caneer[J].Asian Pae J Cancer Prev,2012,13(6) :2873-2877.
  • 5Lin L,Liu A,Peng Z,et al.STAT3 is necessary for proliferation and survival in colon cancer-initiating eells[J].Caneer Res, 2011,71 (23): 7226-7237.
  • 6Yu H,Jove R.The STATs of cancer-new molecular targets come of age[J].Nat Rev Cancer,2004,4(2):97-105.
  • 7Buettner R,Mora L B,Jove R.Activated STAT signaling in human tumors provides novel molecular targets for therapeutic intervention[J]. Clin Cancer Res, 2002,8(4) : 945-954.
  • 8Bromberg J F,Wrzeszczynska M H,Devgan G,et al.Stat3 as an oncngene[J].Cell, 1999,98 ( 3 ) : 295 -303.
  • 9Li Z,Wang C,Prendergast G C,et al.Cyclin D1 functions in cell mi- gration[J].Cell Cycle, 2006,5 (21 ) : 2440-2442.
  • 10Song H,Wang R, Wang S, et al.A low-molecular-weight compound discovered through virtual database screening inhibits stat3 function in breast cancer eells[J].Proc Natl Acad Sci U S A, 2005,102 (13) : 4700- 4705.

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