p63 controls cell migration and invasion by transcriptional regulation of MTSS1

被引:34
作者
Giacobbe, A. [1 ]
Compagnone, M. [1 ]
Bongiorno-Borbone, L. [1 ]
Antonov, A. [2 ]
Markert, E. K. [3 ]
Zhou, J. H. [4 ]
Annicchiarico-Petruzzelli, M. [5 ]
Melino, G. [1 ,2 ]
Peschiaroli, A. [6 ]
机构
[1] Univ Roma Tor Vergata, Dept Expt Med & Surg, Via Montpellier 1, I-00133 Rome, Italy
[2] Univ Leicester, MRC, Toxicol Unit, Leicester, Leics, England
[3] Inst Adv Study, Simons Ctr Syst Biol, Olden Lane, Princeton, NJ 08540 USA
[4] Radboud Univ Nijmegen, Med Ctr Nijmegen, Dept Human Genet, NL-6525 ED Nijmegen, Netherlands
[5] Univ Roma Tor Vergata, Dept Expt Med & Surg, Biochem Lab IDI IRCCS, Rome, Italy
[6] CNR, IBCN, Rome, Italy
基金
英国医学研究理事会;
关键词
BREAST-CANCER; P53; HOMOLOG; METASTASIS; CARCINOMA; SUPPRESSOR; TARGET; TUMORIGENESIS; DELTA-NP63; SURVIVAL; PATHWAY;
D O I
10.1038/onc.2015.230
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
Metastasis is a multistep cell-biological process, which is orchestrated by many factors, including metastasis activators and suppressors. Metastasis Suppressor 1 (MTSS1) was originally identified as a metastasis suppressor protein whose expression is lost in metastatic bladder and prostate carcinomas. However, recent findings indicate that MTSS1 acts as oncogene and pro-migratory factor in melanoma tumors. Here, we identify and characterized a molecular mechanism controlling MTSS1 expression, which impinges on a pro-tumorigenic role of MTSS1 in breast tumors. We found that in normal and in cancer cell lines Delta Np63 is able to drive the expression of MTSS1 by binding to a p63-binding responsive element localized in the MTSS1 locus. We reported that Delta Np63 is able to drive the migration of breast tumor cells by inducing the expression of MTSS1. Notably, in three human breast tumors data sets the MTSS1/p63 co-expression is a negative prognostic factor on patient survival, suggesting that the MTSS1/p63 axis might be functionally important to regulate breast tumor progression.
引用
收藏
页码:1602 / 1608
页数:7
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