Glucose regulated protein 78: A critical link between tumor microenvironment and cancer hallmarks

被引:127
作者
Li, Zongwei [1 ]
Li, Zhuoyu [1 ]
机构
[1] Shanxi Univ, Educ Minist, Key Lab Chem Biol & Mol Engn, Inst Biotechnol, Taiyuan 030006, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2012年 / 1826卷 / 01期
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
Glucose regulated protein 78; Microenvironment; Cancer hallmarks; CELL-SURFACE GRP78; ENDOPLASMIC-RETICULUM CHAPERONE; MESENCHYMAL STEM-CELLS; COOH-TERMINAL DOMAIN; HEAT-SHOCK PROTEINS; BREAST-CANCER; DOWN-REGULATION; REPLICATIVE SENESCENCE; INDUCED APOPTOSIS; CHROMOSOMAL INSTABILITY;
D O I
10.1016/j.bbcan.2012.02.001
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
Glucose regulated protein 78 (GRP78) has long been recognized as a molecular chaperone in the endoplasmic reticulum (ER) and can be induced by the ER stress response. Besides its location in the ER, GRP78 has been found to be present in cell plasma membrane, cytoplasm, mitochondria, nucleus as well as cellular secretions. GRP78 is implicated in tumor cell proliferation, apoptosis resistance, immune escape, metastasis and angiogenesis, and its elevated expression usually correlates with a variety of tumor microenvironmental stresses, including hypoxia, glucose deprivation, lactic acidosis and inflammatory response. GRP78 protein acts as a centrally located sensor of stress, which feels and adapts to the alteration in the tumor microenvironment. This article reviews the potential contributions of GRP78 to the acquisition of cancer hallmarks based on intervening in stress responses caused by tumor niche alterations. The paper also introduces several potential GRP78 relevant targeted therapies. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 22
页数:10
相关论文
共 157 条
[1]   Involvement of the cyclin-dependent kinase inhibitor p16 (INK4a) in replicative senescence of normal human fibroblasts [J].
Alcorta, DA ;
Xiong, Y ;
Phelps, D ;
Hannon, G ;
Beach, D ;
Barrett, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13742-13747
[2]  
[Anonymous], NOVARTIS FDN S
[3]  
[Anonymous], NOVARTIS FDN S
[4]   Cell surface expression of the stress response chaperone GRP78 enables tumor targeting by circulating ligands [J].
Arap, MA ;
Lahdenranta, J ;
Mintz, PJ ;
Hajitou, A ;
Sarkis, AS ;
Arap, W ;
Pasqualini, R .
CANCER CELL, 2004, 6 (03) :275-284
[5]   Glucose-regulated protein 78: A new partner of p53 in trophoblast [J].
Arnaudeau, Serge ;
Arboit, Patrizia ;
Bischof, Paul ;
Shin-ya, Kasuo ;
Tomida, A. ;
Tsuruo, T. ;
Irion, Olivier ;
Cohen, Marie .
PROTEOMICS, 2009, 9 (23) :5316-5327
[6]   Effectiveness of HSV-tk Suicide Gene Therapy Driven by the Grp78 Stress-Inducible Promoter in Esophagogastric Junction and Gastric Adenocarcinomas [J].
Azatian, Armen ;
Yu, Hong ;
Dai, Wande ;
Schneiders, Fiona I. ;
Botelho, Natalia K. ;
Lord, Reginald V. N. .
JOURNAL OF GASTROINTESTINAL SURGERY, 2009, 13 (06) :1044-1051
[7]   Chaperone-Targeting Cytotoxin and Endoplasmic Reticulum Stress-Inducing Drug Synergize to Kill Cancer Cells [J].
Backer, Joseph M. ;
Krivoshein, Arcadius V. ;
Hamby, Carl V. ;
Pizzonia, John ;
Gilbert, Kenneth S. ;
Ray, Yonaton S. ;
Brand, Harrison ;
Paton, Adrienne W. ;
Paton, James C. ;
Backer, Marina V. .
NEOPLASIA, 2009, 11 (11) :1165-U72
[8]   Transcriptional induction of GRP78/BiP by histone deacetylase inhibitors and resistance to histone deacetylase inhibitor-induced apoptosis [J].
Baumeister, Peter ;
Dong, Dezheng ;
Fu, Yong ;
Lee, Amy S. .
MOLECULAR CANCER THERAPEUTICS, 2009, 8 (05) :1086-1094
[9]   Reversal of human cellular senescence:: roles of the p53 and p16 pathways [J].
Beauséjour, CM ;
Krtolica, A ;
Galimi, F ;
Narita, M ;
Lowe, SW ;
Yaswen, P ;
Campisi, J .
EMBO JOURNAL, 2003, 22 (16) :4212-4222
[10]   p53: new roles in metabolism [J].
Bensaad, Karim ;
Vousden, Karen H. .
TRENDS IN CELL BIOLOGY, 2007, 17 (06) :286-291