SIRT1 promotes proliferation and inhibits the senescence-like phenotype in human melanoma cells.
SIRT1 promotes proliferation and inhibits the senescence-like phenotype in human melanoma cells.
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DOI:
10.18632/oncotarget.1791
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发表时间:
2014-04-30
期刊:
影响因子:
--
通讯作者:
Bertolotto C
中科院分区:
文献类型:
--
作者:
Ohanna M;Bonet C;Bille K;Allegra M;Davidson I;Bahadoran P;Lacour JP;Ballotti R;Bertolotto C
SIRT1 operates as both a tumor suppressor and oncogenic factor depending on the cell context. Whether SIRT1 plays a role in melanoma biology remained poorly elucidated. Here, we demonstrate that SIRT1 is a critical regulator of melanoma cell proliferation. SIRT1 suppression by genetic or pharmacological approaches induces cell cycle arrest and a senescence-like phenotype. Gain and loss of function experiments show that M-MITF regulates SIRT1 expression, thereby revealing a melanocyte-specific control of SIRT1. SIRT1 over-expression relieves the senescence-like phenotype and the proliferation arrest caused by MITF suppression, demonstrating that SIRT1 is an effector of MITF-induced proliferation in melanoma cells. Interestingly, SIRT1 level and activity are enhanced in the PLX4032-resistant BRAFV600E-mutated melanoma cells compared with their sensitive counterpart. SIRT1 inhibition decreases melanoma cell growth and rescues the sensibility to PLX4032 of PLX4032-resistant BRAFV600E-mutated melanoma cells. In conclusion, we provide the first evidence that inhibition of SIRT1 warrants consideration as an anti-melanoma therapeutic option.
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影响因子:
64.8
作者:
Bertolotto, Corine;Lesueur, Fabienne;Bressac-de Paillerets, Brigitte
通讯作者:
Bressac-de Paillerets, Brigitte
影响因子:
10.5
作者:
Larribere, L;Hilmi, C;Bertolotto, C
通讯作者:
Bertolotto, C
影响因子:
5.7
作者:
Cerezo, Michael;Tichet, Melanie;Rocchi, Stephane
通讯作者:
Rocchi, Stephane
影响因子:
11.2
作者:
Giuliano, Sandy;Cheli, Yann;Bertolotto, Corine
通讯作者:
Bertolotto, Corine
影响因子:
3.7
作者:
Kabbarah O;Nogueira C;Feng B;Nazarian RM;Bosenberg M;Wu M;Scott KL;Kwong LN;Xiao Y;Cordon-Cardo C;Granter SR;Ramaswamy S;Golub T;Duncan LM;Wagner SN;Brennan C;Chin L
通讯作者:
Chin L