The transcriptional coactivators megakaryoblastic leukemia 1/2 mediate the effects of loss of the tumor suppressor deleted in liver cancer 1

被引:42
作者
Muehlich, S. [1 ]
Hampl, V. [1 ]
Khalid, S. [1 ]
Singer, S. [2 ]
Frank, N. [1 ]
Breuhahn, K. [2 ]
Gudermann, T. [1 ]
Prywes, R. [3 ]
机构
[1] Univ Munich, Walther Straub Inst Pharmacol & Toxicol, D-80336 Munich, Germany
[2] Univ Heidelberg Hosp, Inst Pathol, Heidelberg, Germany
[3] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
关键词
DLC1; MKL1; MKL2; MRTF; Rho; SRF; SERUM RESPONSE FACTOR; TISSUE GROWTH-FACTOR; HEPATOCELLULAR-CARCINOMA; HUMAN HEPATOCARCINOGENESIS; ACTIN CYTOSKELETON; CELL-MIGRATION; TARGET GENES; METASTASIS; SRF; PROGRESSION;
D O I
10.1038/onc.2011.560
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Deleted in Liver Cancer 1 (DLC1) is a tumor suppressor whose allele is lost in 50% of liver, breast, lung and 70% of colon cancers. Here, we show that the transcriptional coactivators Megakaryoblastic Leukemia 1 and 2 (MKL1/2) are constitutively localized to the nucleus in hepatocellular and mammary carcinoma cells that lack DLC1. Moreover, DLC1 loss and MKL1 nuclear localization correlate in primary human hepatocellular carcinoma. Nuclear accumulation of MKL1 in DLC1 deficient cancer cells is accomplished by activation of the RhoA/actin signaling pathway and concomitant impairment of MKL1 phosphorylation, which results in constitutive activation of MKL1/2 target genes. We provide evidence that MKL1/2 mediates cancerous transformation in DLC1-deficient hepatocellular and mammary carcinoma cells. Depletion of MKL1/2 suppresses cell migration, cell proliferation and anchorage-independent cell growth induced by DLC1 loss. Oncogene (2012) 31, 3913-3923; doi:10.1038/onc.2011.560; published online 5 December 2011
引用
收藏
页码:3913 / 3923
页数:11
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