The role of S6K1 in ER-positive breast cancer

被引:56
作者
Holz, Marina K. [1 ,2 ]
机构
[1] Yeshiva Univ, Stern Coll Women, Dept Biol, New York, NY 10033 USA
[2] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10467 USA
关键词
mTORC1; S6K1; ER alpha; estrogen; rapamycin; 17q23; amplicon; ESTROGEN-RECEPTOR-ALPHA; ENDOCRINE THERAPY RESISTANCE; CELL-CYCLE PROGRESSION; MTOR SIGNALING PATHWAY; GENE-EXPRESSION; ANTIESTROGEN RESISTANCE; MEDIATED DEGRADATION; TUBEROUS SCLEROSIS; 17Q23; AMPLICON; COPY NUMBER;
D O I
10.4161/cc.21194
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The 40S ribosomal S6 kinase 1 (S6K1) is a conserved serine/threonine protein kinase that belongs to the AGC family of protein kinases, which also includes Akt and many others. S6K1 is the principal kinase effector downstream of the mammalian target of rapamycin complex 1 (mTORC1). S6K1 is sensitive to a wide range of signaling inputs, including growth factors, amino acids, energy levels and hypoxia. S6K1 relays these signals to regulate a growing list of substrates and interacting proteins in control of oncogenic processes, such as cell growth and proliferation, cell survival and apoptosis and cell migration and invasion. Several lines of evidence suggest an important role for S6K1 in estrogen receptor (ER)-positive breast cancer. S6K1 directly phosphorylates and activates ER alpha. Furthermore, S6K1 expression is estrogenically regulated. Therefore, hyperactivation of mTORC1/S6K1 signaling may be closely related to ER-positive status in breast cancer and may be utilized as a marker for prognosis and a therapeutic target.
引用
收藏
页码:3159 / 3165
页数:7
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