Kinase requirements in human cells: IV. Differential kinase requirements in cervical and renal human tumor cell lines

被引:27
作者
Grueneberg, Dorre A. [1 ]
Li, Wenliang [1 ]
Davies, Joan E. [1 ]
Sawyer, Jacqueline [1 ]
Pearlberg, Joseph [1 ]
Harlow, Ed [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
关键词
cervical cancer cells; essential kinases; renal cancer cells; shRNA screens; fingerprints;
D O I
10.1073/pnas.0806578105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Functional differences among human cells have been difficult to identify by standard biochemical methods. Loss-of-function shRNA screens provide an unbiased method to compare protein requirements across cell lines. In previous work, we have studied kinase requirements in two settings, either among a panel of cells from numerous tissues or between two cell lines that differ only by the expression of a chosen oncoprotein or tumor suppressor protein. Here we examine the patterns of kinase requirements between two unrelated cells, the cervical carcinoma cell line HeLa and the renal carcinoma cell line 786-O. By using time courses of cell proliferation after shRNA transduction and by introducing different levels of the shRNAs, we were able to carefully compare the kinase requirements. These comparisons identified 10 kinases that were required in HeLa but not 786-O, and 5 kinases that were required in 786-O but not HeLa. The patterns of growth inhibition due to particular sets of shRNAs in a tumor cell line were shown to be similar in some but not all cell lines derived from the same tissue-specific cancer type. Differential kinase requirements promise to be useful in distinguishing important cell-to-cell functional variations and may lead to the identification of fingerprints for different physiological cell states.
引用
收藏
页码:16490 / 16495
页数:6
相关论文
共 24 条
[21]   Lentivirus-delivered stable gene silencing by RNAi in primary cells [J].
Stewart, SA ;
Dykxhoorn, DM ;
Palliser, D ;
Mizuno, H ;
Yu, EY ;
An, DS ;
Sabatini, DM ;
Chen, ISY ;
Hahn, WC ;
Sharp, PA ;
Weinberg, RA ;
Novina, CD .
RNA, 2003, 9 (04) :493-501
[22]   Perspective: machines for RNAi [J].
Tomari, Y ;
Zamore, PD .
GENES & DEVELOPMENT, 2005, 19 (05) :517-529
[23]   A genetic screen for candidate tumor suppressors identifies REST [J].
Westbrook, TF ;
Martin, ES ;
Schlabach, MR ;
Leng, YM ;
Liang, AC ;
Feng, B ;
Zhao, JJ ;
Roberts, TM ;
Mandel, G ;
Hannon, GJ ;
DePinho, RA ;
Chin, L ;
Elledge, SJ .
CELL, 2005, 121 (06) :837-848
[24]   An approach to genomewide screens of expressed small interfering RNAs in mammalian cells [J].
Zheng, LX ;
Liu, J ;
Batalov, S ;
Zhou, DM ;
Orth, A ;
Ding, S ;
Schultz, PG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (01) :135-140