Departments of Microbiology, Cell Biology, and Biomedical Engineering, Cardiovascular Research Center and Mellon Urological Cancer Research Institute, University of Virginia, Charlottesville, VA 22908, USA.
Mol Biol Cell. 2010 Feb 15;21(4):499-500. doi: 10.1091/mbc.e09-07-0602.
In 1992, Jere Meredith and I followed up on a serendipitous observation and showed that matrix deprivation can lead to apoptosis. Our article in Molecular Biology of the Cell, together with work form Steve Frisch's lab, helped establish the paradigm that integrin signals control cell survival in a variety of systems. It has been a pleasure to watch that work take on a life of its own as other investigators have explored its role in processes such as cavitation, regression of the mammary gland at the end of pregnancy, cancer metastasis, and tumor resistance to chemotherapy. Recently, we described an exception to the paradigm: In some tumors, reagents that activate integrin signaling enhance apoptosis in response to chemotherapy.
1992 年,Jere Meredith 和我对一个偶然的观察结果进行了跟进,结果表明基质剥夺会导致细胞凋亡。我们在《Molecular Biology of the Cell》上发表的文章,以及 Steve Frisch 实验室的工作,有助于确立这样一种模式,即整合素信号在各种系统中控制细胞存活。当其他研究人员探索其在空泡形成、妊娠末期乳腺退化、癌症转移和肿瘤对化疗的耐药性等过程中的作用时,很高兴看到这项工作有了自己的生命。最近,我们描述了一个例外:在某些肿瘤中,激活整合素信号的试剂会增强对化疗的细胞凋亡反应。