Stress signaling and the shaping of the mammary tissue in development and cancer

被引:21
作者
Avivar-Valderas, A. [1 ,2 ,3 ]
Wen, H. C. [3 ,4 ]
Aguirre-Ghiso, J. A. [1 ,2 ,3 ,5 ]
机构
[1] Mt Sinai Sch Med, Dept Med, Div Hematol & Oncol, New York, NY 10029 USA
[2] Mt Sinai Sch Med, Dept Otolaryngol, New York, NY 10029 USA
[3] Mt Sinai Sch Med, Tisch Canc Inst, New York, NY 10029 USA
[4] Mt Sinai Sch Med, Dept Oncol Sci, New York, NY 10029 USA
[5] Mt Sinai Sch Med, Black Family Stem Cell Inst, New York, NY 10029 USA
关键词
stress; anoikis; mammary gland; ECM; breast cancer; autophagy; UNFOLDED PROTEIN RESPONSE; EXTRACELLULAR-MATRIX DETACHMENT; ANCHORAGE-DEPENDENT FIBROBLASTS; HEAT-SHOCK PROTEINS; P38 MAP KINASE; EPITHELIAL-CELLS; BREAST-CANCER; ER STRESS; LUMEN FORMATION; TUMOR-GROWTH;
D O I
10.1038/onc.2013.554
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
The postnatal mammary gland develops extensively through cycles of proliferation, branching, involution and remodeling. We review recent advances made in the field of stress signaling pathways and its roles in mammary gland organogenesis, how they contribute to normal organ specification and homeostasis and how its subversion by oncogenes leads to cancer. We analyze stress signaling in mammary gland biology taking into account the interrelationship with the extracellular matrix and adhesion signaling during morphogenesis. By integrating the information gathered from in vivo and three dimensional in vitro organogenesis studies, we review the novel contribution of p38(SAPK), c-Jun NH2-terminal kinase and PKR-like endoplasmic reticulum kinase ( PERK) signaling pathways to the timely activation of cell death, correct establishment of polarity and growth arrest and autophagy, respectively. We also review the evidence supporting that the activation of the aforementioned stress kinases maintain breast acinar structures as part of a tumor suppressive program and that its deregulation is commonplace during breast cancer initiation.
引用
收藏
页码:5483 / 5490
页数:8
相关论文
共 112 条
[1]   Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21 [J].
Aita, VM ;
Liang, XH ;
Murty, VVVS ;
Pincus, DL ;
Yu, WP ;
Cayanis, E ;
Kalachikov, S ;
Gilliam, TC ;
Levine, B .
GENOMICS, 1999, 59 (01) :59-65
[2]   MYBBP1A suppresses breast cancer tumorigenesis by enhancing the p53 dependent anoikis [J].
Akaogi, Kensuke ;
Ono, Wakana ;
Hayashi, Yuki ;
Kishimoto, Hiroyuki ;
Yanagisawa, Junn .
BMC CANCER, 2013, 13
[3]   Extracellular proteolysis in transgenic mouse models of breast cancer [J].
Almholt, Kasper ;
Green, Kirsty Anne ;
Juncker-Jensen, Anna ;
Nielsen, Boye Schnack ;
Lund, Leif Roge ;
Romer, John .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 2007, 12 (01) :83-97
[4]   Regulation of autophagy during ECM detachment is linked to a selective inhibition of mTORC1 by PERK [J].
Avivar-Valderas, A. ;
Bobrovnikova-Marjon, E. ;
Diehl, J. Alan ;
Bardeesy, N. ;
Debnath, J. ;
Aguirre-Ghiso, J. A. .
ONCOGENE, 2013, 32 (41) :4932-4940
[5]   PERK Integrates Autophagy and Oxidative Stress Responses To Promote Survival during Extracellular Matrix Detachment [J].
Avivar-Valderas, Alvaro ;
Salas, Eduardo ;
Bobrovnikova-Marjon, Ekaterina ;
Diehl, J. Alan ;
Nagi, Chandandeep ;
Debnath, Jayanta ;
Aguirre-Ghiso, Julio A. .
MOLECULAR AND CELLULAR BIOLOGY, 2011, 31 (17) :3616-3629
[6]   Roles of p38 MAPKs in invasion and metastasis [J].
Barrantes, Ivan del Barco ;
Nebreda, Angel R. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2012, 40 :79-84
[7]   Mammalian G1- and S-phase checkpoints in response to DNA damage [J].
Bartek, J ;
Lukas, J .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (06) :738-747
[8]   Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations [J].
Bateman, John F. ;
Boot-Handford, Raymond P. ;
Lamande, Shireen R. .
NATURE REVIEWS GENETICS, 2009, 10 (03) :173-183
[9]   CONTROL OF MESSENGER-RNA PRODUCTION, TRANSLATION AND TURNOVER IN SUSPENDED AND REATTACHED ANCHORAGE-DEPENDENT FIBROBLASTS [J].
BENECKE, BJ ;
BENZEEV, A ;
PENMAN, S .
CELL, 1978, 14 (04) :931-939
[10]   IDENTIFICATION OF NOVEL PHOSPHORYLATION SITES REQUIRED FOR ACTIVATION OF MAPKAP KINASE-2 [J].
BENLEVY, R ;
LEIGHTON, IA ;
DOZA, YN ;
ATTWOOD, P ;
MORRICE, N ;
MARSHALL, CJ ;
COHEN, P .
EMBO JOURNAL, 1995, 14 (23) :5920-5930