Hishikawa K, Oemar B S, Tanner F C, Nakaki T, Lüscher T F, Fujii T
Department of Pharmacology, Teikyo University School of Medicine, Tokyo 173-8605, Japan.
J Biol Chem. 1999 Dec 24;274(52):37461-6. doi: 10.1074/jbc.274.52.37461.
Connective tissue growth factor (CTGF) is a member of an emerging CCN gene family that is implicated in various diseases associated with fibro-proliferative disorder including scleroderma and atherosclerosis. The function of CTGF in human cancer is largely unknown. We now show that CTGF induces apoptosis in the human breast cancer cell line MCF-7. CTGF mRNA was completely absent in MCF-7 but strongly induced by treatment with transforming growth factor beta (TGF-beta). TGF-beta by itself induced apoptosis in MCF-7, and this effect was reversed by co-treatment with CTGF antisense oligonucleotide. Overexpression of CTGF gene in transiently transfected MCF-7 cells significantly augmented apoptosis. Moreover, recombinant CTGF protein significantly enhanced apoptosis in MCF-7 cells as evaluated by DNA fragmentation, Tdt-mediated dUTP biotin nick end-labeling staining, flow cytometry analysis, and nuclear staining using Hoechst 33258. Finally, recombinant CTGF showed no effect on Bax protein expression but significantly reduced Bcl2 protein expression. Taken together, these results suggest that CTGF is a major inducer of apoptosis in the human breast cancer cell line MCF-7 and that TGF-beta-induced apoptosis in MCF-7 cells is mediated, in part, by CTGF.
结缔组织生长因子(CTGF)是新兴的CCN基因家族的成员,该家族与包括硬皮病和动脉粥样硬化在内的各种与纤维增殖性疾病相关的疾病有关。CTGF在人类癌症中的功能在很大程度上尚不清楚。我们现在表明,CTGF可诱导人乳腺癌细胞系MCF-7凋亡。MCF-7中完全不存在CTGF mRNA,但用转化生长因子β(TGF-β)处理可强烈诱导其表达。TGF-β本身可诱导MCF-7凋亡,而与CTGF反义寡核苷酸共同处理可逆转这种效应。在瞬时转染的MCF-7细胞中CTGF基因的过表达显著增强了凋亡。此外,通过DNA片段化、TdT介导的dUTP生物素缺口末端标记染色、流式细胞术分析以及使用Hoechst 33258进行核染色评估,重组CTGF蛋白显著增强了MCF-7细胞的凋亡。最后,重组CTGF对Bax蛋白表达无影响,但显著降低了Bcl2蛋白表达。综上所述,这些结果表明CTGF是人乳腺癌细胞系MCF-7凋亡的主要诱导因子,并且TGF-β诱导的MCF-7细胞凋亡部分是由CTGF介导的。