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Dual Roles of RNF2 in Melanoma Progression.

Authors :
Rai K
Akdemir KC
Kwong LN
Fiziev P
Wu CJ
Keung EZ
Sharma S
Samant NS
Williams M
Axelrad JB
Shah A
Yang D
Grimm EA
Barton MC
Milton DR
Heffernan TP
Horner JW
Ekmekcioglu S
Lazar AJ
Ernst J
Chin L
Source :
Cancer discovery [Cancer Discov] 2015 Dec; Vol. 5 (12), pp. 1314-27. Date of Electronic Publication: 2015 Oct 08.
Publication Year :
2015

Abstract

Unlabelled: Epigenetic regulators have emerged as critical factors governing the biology of cancer. Here, in the context of melanoma, we show that RNF2 is prognostic, exhibiting progression-correlated expression in human melanocytic neoplasms. Through a series of complementary gain-of-function and loss-of-function studies in mouse and human systems, we establish that RNF2 is oncogenic and prometastatic. Mechanistically, RNF2-mediated invasive behavior is dependent on its ability to monoubiquitinate H2AK119 at the promoter of LTBP2, resulting in silencing of this negative regulator of TGFβ signaling. In contrast, RNF2's oncogenic activity does not require its catalytic activity nor does it derive from its canonical gene repression function. Instead, RNF2 drives proliferation through direct transcriptional upregulation of the cell-cycle regulator CCND2. We further show that MEK1-mediated phosphorylation of RNF2 promotes recruitment of activating histone modifiers UTX and p300 to a subset of poised promoters, which activates gene expression. In summary, RNF2 regulates distinct biologic processes in the genesis and progression of melanoma via different molecular mechanisms.<br />Significance: The role of epigenetic regulators in cancer progression is being increasingly appreciated. We show novel roles for RNF2 in melanoma tumorigenesis and metastasis, albeit via different mechanisms. Our findings support the notion that epigenetic regulators, such as RNF2, directly and functionally control powerful gene networks that are vital in multiple cancer processes.<br /> (©2015 American Association for Cancer Research.)

Details

Language :
English
ISSN :
2159-8290
Volume :
5
Issue :
12
Database :
MEDLINE
Journal :
Cancer discovery
Publication Type :
Academic Journal
Accession number :
26450788
Full Text :
https://doi.org/10.1158/2159-8290.CD-15-0493