A prototypic matricellular protein in the tumor

被引:95
作者
Clark, Clancy J. [2 ]
Sage, E. Helene [1 ]
机构
[1] Benaroya Res Inst Virginia Mason, Seattle, WA 98101 USA
[2] Virginia Mason Med Ctr, Dept Gen Surg, Seattle, WA 98101 USA
关键词
tumor microenvironment; SPARC; matricellular protein; angiogenesis; desmoplasia;
D O I
10.1002/jcb.21688
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
Within the tumor microenvironment is a dynamic exchange between cancer cells and their surrounding stroma. This complex biologic system requires carefully designed models to understand the role of its stromal components in carcinogenesis, tumor progression, invasion, and metastasis. Secreted protein acidic and rich in cysteine (SPARC) is a prototypic matricellular protein at the center of this exchange. Two decades of basic science research combined with recent whole genome analyses indicate that SPARC is an important player in vertebrate evolution, normal development, and maintenance of normal tissue homeostasis. Therefore, SPARC might also play an important role in the tumor microenvironment. Clinical evidence indicates that SPARC expression correlates with tumor progression, but tightly controlled animal models have shown that the role of SPARC in tumor progression is dependent on tissue and tumor cell type. In this Prospectus, we review the current understanding of SPARC in the tumor microenvironment and discuss current and future investigations of SPARC and tumor-stromal interactions that require careful consideration of growth factors, cytokines, proteinases, and angiotropic factors that might influence SPARC activity and tumor progression.
引用
收藏
页码:721 / 732
页数:12
相关论文
共 113 条
[1]   Systems biology: Its practice and challenges [J].
Aderem, A .
CELL, 2005, 121 (04) :511-513
[2]   The tumour microenvironment as a target for chemoprevention [J].
Albini, Adriana ;
Sporn, Michael B. .
NATURE REVIEWS CANCER, 2007, 7 (02) :139-147
[3]   Physicochemical modelling of cell signalling pathways [J].
Aldridge, Bree B. ;
Burke, John M. ;
Lauffenburger, Douglas A. ;
Sorger, Peter K. .
NATURE CELL BIOLOGY, 2006, 8 (11) :1195-1203
[4]   Molecular characterization of the tumor microenvironment in breast cancer [J].
Allinen, M ;
Beroukhim, R ;
Cai, L ;
Brennan, C ;
Lahti-Domenici, J ;
Huang, HY ;
Porter, D ;
Hu, M ;
Chin, L ;
Richardson, A ;
Schnitt, S ;
Sellers, WR ;
Polyak, K .
CANCER CELL, 2004, 6 (01) :17-32
[5]   Secreted protein acidic and rich in cysteine produced by human melanoma cells modulates polymorphonuclear leukocyte recruitment and antitumor cytotoxic capacity [J].
Alvarez, MJ ;
Prada, F ;
Salvatierra, E ;
Bravo, AI ;
Lutzky, VP ;
Carbone, C ;
Pitossi, FJ ;
Chuluyan, HE ;
Podhajcer, OL .
CANCER RESEARCH, 2005, 65 (12) :5123-5132
[6]   Tumor morphology and phenotypic evolution driven by selective pressure from the microenvironment [J].
Anderson, Alexander R. A. ;
Weaver, Alissa M. ;
Cummings, Peter T. ;
Quaranta, Vito .
CELL, 2006, 127 (05) :905-915
[7]   Development of UV-induced squamous cell carcinomas is suppressed in the absence of SPARC [J].
Aycock, RL ;
Bradshaw, AC ;
Sage, EH ;
Starcher, B .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 123 (03) :592-599
[8]   Matricellular homologs in the foreign body response - Hevin suppresses inflammation, but Hevin and SPARC together diminish angiogenesis [J].
Barker, TH ;
Framson, P ;
Puolakkainen, PA ;
Reed, M ;
Funk, SE ;
Sage, EH .
AMERICAN JOURNAL OF PATHOLOGY, 2005, 166 (03) :923-933
[9]  
BELLAHCENE A, 1995, AM J PATHOL, V146, P95
[10]   Stromal osteonectin overexpression is associated with poor outcome in patients with ampullary cancer [J].
Bloomston, Mark ;
Ellison, E. Christopher ;
Muscarella, Peter ;
Al-Saif, Osama ;
Martin, Edward W. ;
Melvin, W. Scott ;
Frankel, Wendy L. .
ANNALS OF SURGICAL ONCOLOGY, 2007, 14 (01) :211-217