A Synthetic Lethal Interaction between K-Ras Oncogenes and Cdk4 Unveils a Therapeutic Strategy for Non-small Cell Lung Carcinoma

被引:357
作者
Puyol, Marta [1 ]
Martin, Alberto [1 ]
Dubus, Pierre [4 ]
Mulero, Francisca [2 ]
Pizcueta, Pilar [3 ]
Khan, Gulfaraz [5 ]
Guerra, Carmen [1 ]
Santamaria, David [1 ]
Barbacid, Mariano [1 ]
机构
[1] CNIO, Mol Oncol Programme, E-28029 Madrid, Spain
[2] CNIO, Biotechnol Programme, E-28029 Madrid, Spain
[3] CNIO, Expt Therapeut Programme, E-28029 Madrid, Spain
[4] Univ Bordeaux 2, EA2406, F-33076 Bordeaux, France
[5] United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Microbiol & Immunol, Al Ain, U Arab Emirates
关键词
CHROMOSOME; 12P; MUTATION; CANCER; CYCLE; SENESCENCE; P53; SUPPRESSION; INHIBITION; P27(KIP1); KRAS2;
D O I
10.1016/j.ccr.2010.05.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have unveiled a synthetic lethal interaction between K-Ras oncogenes and Cdk4 in a mouse tumor model that closely recapitulates human non-small cell lung carcinoma (NSCLC). Ablation of Cdk4, but not Cdk2 or Cdk6, induces an immediate senescence response only in lung cells that express an endogenous K-Ras oncogene. No such response occurs in lungs expressing a single Cdk4 allele or in other K-Ras-expressing tissues. More importantly, targeting Cdk4 alleles in advanced tumors detectable by computed tomography scanning also induces senescence and prevents tumor progression. These observations suggest that robust and selective pharmacological inhibition of Cdk4 may provide therapeutic benefit for NSCLC patients carrying K-RAS oncogenes.
引用
收藏
页码:63 / 73
页数:11
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