Multifaceted roles of adiponectin in cancer

被引:68
作者
Hebbard, Lionel [1 ,2 ]
Ranscht, Barbara [3 ]
机构
[1] Westmead Millennium Inst, Storr Liver Unit, Westmead, NSW 2145, Australia
[2] Univ Sydney, Westmead, NSW 2145, Australia
[3] Sanford Burnham Med Res Inst, NIH Designated Canc Ctr, Tumor Microenvironm Program, La Jolla, CA 92037 USA
基金
英国医学研究理事会;
关键词
Adiponectin; AdipoR1; AdipoR2; T-cadherin; cancer; signaling; ACTIVATED PROTEIN-KINASE; COA-CARBOXYLASE-ALPHA; T-CADHERIN; PLASMA ADIPONECTIN; INSULIN-RESISTANCE; ADIPOSE-TISSUE; STIMULATES ANGIOGENESIS; MOLECULAR-MECHANISMS; SIGNAL-TRANSDUCTION; TUMOR-GROWTH;
D O I
10.1016/j.beem.2013.11.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity is linked to increased cancer risk. Pathological expansion of adipose tissue impacts adipocyte function and secretion of hormonal factors regulating tissue homeostasis and metabolism. Adiponectin is an adipocyte-secreted, circulating hormone with pleiotropic functions in lipid and glucose metabolism, and beneficial roles in cardiovascular functions and inflammation. In obesity, decreased Adiponectin plasma levels correlate with tumor development and progression. The association of Adiponectin with potential tumor-limiting functions has raised significant interest in exploring this adipokine as a target for cancer-diagnostic and therapeutic applications. Recent studies, however, also implicate Adiponectin in supporting malignancy. This review highlights the evidence that links Adiponectin signaling to either cancer-protective or cancer-supporting functions. In this context, we discuss Adiponectin interactions with its receptors and associated signaling pathways. Despite significant advances in understanding Adiponectin functions and signaling mechanisms, its role in cancer remains multifaceted and subject to controversy. (C) 2013 Published by Elsevier Ltd.
引用
收藏
页码:59 / 69
页数:11
相关论文
共 103 条
[71]   T-CADHERIN, A NOVEL CADHERIN CELL-ADHESION MOLECULE IN THE NERVOUS-SYSTEM LACKS THE CONSERVED CYTOPLASMIC REGION [J].
RANSCHT, B ;
DOURSZIMMERMANN, MT .
NEURON, 1991, 7 (03) :391-402
[72]  
Ranscht B., 2003, HDB CELL SIGNALING, P889
[73]   Sialic Acid Modification of Adiponectin Is Not Required for Multimerization or Secretion but Determines Half-Life in Circulation [J].
Richards, Ayanthi A. ;
Colgrave, Michelle L. ;
Zhang, Jialiang ;
Webster, Julie ;
Simpson, Fiona ;
Preston, Elaine ;
Wilks, Donna ;
Hoehn, Kyle L. ;
Stephenson, Matthew ;
Macdonald, Graeme A. ;
Prins, John B. ;
Cooney, Gregory J. ;
Xu, Aimin ;
Whitehead, Jonathan P. .
MOLECULAR ENDOCRINOLOGY, 2010, 24 (01) :229-239
[74]   A NOVEL SERUM-PROTEIN SIMILAR TO C1Q, PRODUCED EXCLUSIVELY IN ADIPOCYTES [J].
SCHERER, PE ;
WILLIAMS, S ;
FOGLIANO, M ;
BALDINI, G ;
LODISH, HF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :26746-26749
[75]   Plasma adiponectin complexes have distinct biochemical characteristics [J].
Schraw, Todd ;
Wang, Zhao V. ;
Halberg, Nils ;
Hawkins, Meredith ;
Scherer, Philipp E. .
ENDOCRINOLOGY, 2008, 149 (05) :2270-2282
[76]   Regulation of the mTOR Complex 1 Pathway by Nutrients, Growth Factors, and Stress [J].
Sengupta, Shomit ;
Peterson, Timothy R. ;
Sabatini, David M. .
MOLECULAR CELL, 2010, 40 (02) :310-322
[77]   The LKB1-AMPK pathway: metabolism and growth control in tumour suppression [J].
Shackelford, David B. ;
Shaw, Reuben J. .
NATURE REVIEWS CANCER, 2009, 9 (08) :563-575
[78]   The crystal structure of a complement-1q family protein suggests an evolutionary link to tumor necrosis factor [J].
Shapiro, L ;
Scherer, PE .
CURRENT BIOLOGY, 1998, 8 (06) :335-338
[79]   Adiponectin Antagonizes the Oncogenic Actions of Leptin in Hepatocellular Carcinogenesis [J].
Sharma, Dipali ;
Wang, Jason ;
Fu, Ping P. ;
Sharma, Shvetank ;
Nagalingam, Arumugam ;
Mells, Jamie ;
Handy, Jeffrey ;
Page, Andrew J. ;
Cohen, Cynthia ;
Anania, Frank A. ;
Saxena, Neeraj K. .
HEPATOLOGY, 2010, 52 (05) :1713-1722
[80]   Ras, PI(3)K and mTOR signalling controls tumour cell growth [J].
Shaw, Reuben J. ;
Cantley, Lewis C. .
NATURE, 2006, 441 (7092) :424-430