Grueneberg Dorre A, Degot Sebastien, Pearlberg Joseph, Li Wenliang, Davies Joan E, Baldwin Amy, Endege Wilson, Doench John, Sawyer Jacqueline, Hu Yanhui, Boyce Frederick, Xian Jun, Munger Karl, Harlow Ed
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2008 Oct 28;105(43):16472-7. doi: 10.1073/pnas.0808019105. Epub 2008 Oct 23.
shRNA loss-of-function screens were used to identify kinases that were rate-limiting for promoting cell proliferation and survival. Here, we study the differences in kinase requirements among various human cells, including freshly prepared primary cells, isogenic cells, immortalized cells, and cancer cell lines. Closely related patterns of kinase requirements among the various cell types were observed in three cases: (i) in repeat experiments using the same cells, (ii) with multiple populations of freshly prepared primary epithelial cells isolated from the same tissue source, and (iii) between nearly isogenic cells that differ from each other by the expression of a single gene. Other commonly used cancer cell lines were distinct from one another, even when they were isolated from similar tumor types. Even primary cells of different lineages isolated from the same tissue source showed many differences. The differences in kinase requirements among cell lines observed in this study suggest that the control of proliferation and survival may be significantly different between cell lines and that simple comparisons from any one cell to another may be misleading. Although the regulation of cell proliferation and survival are heavily studied areas, we did not see a bias in these screens toward the identification of previously known and well studied kinases, suggesting that our knowledge of molecular events in these areas is still meager.
使用短发夹RNA(shRNA)功能缺失筛选来鉴定对促进细胞增殖和存活具有限速作用的激酶。在此,我们研究了各种人类细胞之间激酶需求的差异,这些细胞包括新鲜制备的原代细胞、同基因细胞、永生化细胞和癌细胞系。在三种情况下观察到了不同细胞类型之间密切相关的激酶需求模式:(i)在使用相同细胞的重复实验中,(ii)从同一组织来源分离的多个新鲜制备的原代上皮细胞群体中,以及(iii)在仅因单个基因表达不同而彼此有差异的近同基因细胞之间。其他常用的癌细胞系彼此不同,即使它们是从相似的肿瘤类型中分离出来的。即使是从同一组织来源分离的不同谱系的原代细胞也显示出许多差异。本研究中观察到的细胞系之间激酶需求的差异表明,细胞系之间增殖和存活的调控可能存在显著差异,并且从任何一个细胞到另一个细胞的简单比较可能会产生误导。尽管细胞增殖和存活的调控是研究重点领域,但我们在这些筛选中并未发现偏向于鉴定先前已知且深入研究的激酶的倾向,这表明我们在这些领域对分子事件的了解仍然匮乏。