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

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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Mühlich, Susanne (VerfasserIn) , Singer, Stephan (VerfasserIn) , Breuhahn, Kai (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2012
In: Oncogene
Year: 2011, Jahrgang: 31, Heft: 35, Pages: 3913-3923
ISSN:1476-5594
DOI:10.1038/onc.2011.560
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1038/onc.2011.560
Verlag, Volltext: https://www.nature.com/articles/onc2011560
Volltext
Verfasserangaben:S. Muehlich, V. Hampl, S. Khalid, S. Singer, N. Frank, K. Breuhahn, T. Gudermann, R. Prywes
Beschreibung
Zusammenfassung: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.
Beschreibung:Published online: 05 December 2011
Gesehen am 24.05.2018
Beschreibung:Online Resource
ISSN:1476-5594
DOI:10.1038/onc.2011.560