Cellular context-dependent "colors" of transforming growth factor-β signaling

被引:71
作者
Ikushima, Hiroaki [1 ]
Miyazono, Kohei [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo, Japan
来源
CANCER SCIENCE | 2010年 / 101卷 / 02期
基金
日本学术振兴会;
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; HORMONE-RELATED PROTEIN; TGF-BETA; MAMMARY-CARCINOMA; STEM-CELLS; DISEASE PROGRESSION; CANCER PROGRESSION; GASTRIC-CARCINOMA; TUMOR SUPPRESSION; KINASE INHIBITOR;
D O I
10.1111/j.1349-7006.2009.01441.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Transforming growth factor (TGF)-beta signaling has interesting characteristics in the context of cancer. Although perturbations of TGF-beta signaling are strongly implicated in cancer progression, TGF-beta signaling has both tumor-suppressive and tumor-promoting effects. For example, TGF-beta inhibits cancer cell proliferation in some cellular contexts, but promotes it in others. Although several approaches to treating cancer have been considered using TGF-beta-based therapeutic strategies, the contradictory behaviors of TGF-beta have made these approaches complex. To put them to practical use, either the tumor-suppressive or tumor-promoting arm needs to be specifically manipulated. However, there is virtually no method to specifically regulate a certain cell response induced by TGF-beta. In this review, we first consider the basic machinery of TGF-beta signaling, and describe several cell responses induced by TGF-beta stimulation in specific contexts. Mechanisms by which TGF-beta can induce several responses in a cellular context-dependent fashion are discussed with established paradigms and models. We also address perspectives on the specific control of only a subset of numerous cell responses induced by TGF-beta stimulation. Such methods will aid specific regulation of either the tumor-suppressive or tumor-promoting arm of the TGF-beta pathway and in realization of TGF-beta-based treatment of malignant tumors. (Cancer Sci 2010; 101: 306-312).
引用
收藏
页码:306 / 312
页数:7
相关论文
共 71 条
[1]   A Mutant-p53/Smad Complex Opposes p63 to Empower TGFβ-Induced Metastasis [J].
Adorno, Maddalena ;
Cordenonsi, Michelangelo ;
Montagner, Marco ;
Dupont, Sirio ;
Wong, Christine ;
Hann, Byron ;
Solari, Aldo ;
Bobisse, Sara ;
Rondina, Maria Beatrice ;
Guzzardo, Vincenza ;
Parenti, Anna R. ;
Rosato, Antonio ;
Bicciato, Silvio ;
Balmain, Allan ;
Piccolo, Stefano .
CELL, 2009, 137 (01) :87-98
[2]   TGF-β signaling in fibroblasts modulates the oncogenic potential of adjacent epithelia [J].
Bhowmick, NA ;
Chytil, A ;
Plieth, D ;
Gorska, AE ;
Dumont, N ;
Shappell, S ;
Washington, MK ;
Neilson, EG ;
Moses, HL .
SCIENCE, 2004, 303 (5659) :848-851
[3]   TGFβ:: the molecular Jekyll and Hyde of cancer [J].
Bierie, Brian ;
Moses, Harold L. .
NATURE REVIEWS CANCER, 2006, 6 (07) :506-520
[4]   High TGFβ-Smad activity confers poor prognosis in glioma patients and promotes cell proliferation depending on the methylation of the PDGF-B gene [J].
Bruna, Alejandra ;
Darken, Rachel S. ;
Rojo, Federico ;
Ocana, Alberto ;
Penuelas, Silvia ;
Arias, Alexandra ;
Paris, Raquel ;
Tortosa, Avelina ;
Mora, Jaume ;
Baselga, Jose ;
Seoane, Joan .
CANCER CELL, 2007, 11 (02) :147-160
[5]   Loss of TGF-β type II receptor in fibroblasts promotes mammary carcinoma growth and invasion through upregulation of TGF-α-, MSP- and HGF-mediated signaling networks [J].
Cheng, N ;
Bhowmick, NA ;
Chytil, A ;
Gorksa, AE ;
Brown, KA ;
Muraoka, R ;
Arteaga, CL ;
Neilson, EG ;
Hayward, SW ;
Moses, HL .
ONCOGENE, 2005, 24 (32) :5053-5068
[6]  
DALAL BI, 1993, AM J PATHOL, V143, P381
[7]   TRANSFORMING GROWTH-FACTOR-BETA INDUCES THE CYCLIN-DEPENDENT KINASE INHIBITOR P21 THROUGH A P53-INDEPENDENT MECHANISM [J].
DATTO, MB ;
LI, Y ;
PANUS, JF ;
HOWE, DJ ;
XIONG, Y ;
WANG, XF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5545-5549
[8]   TGF-β signaling in tumor suppression and cancer progression [J].
Derynck, R ;
Akhurst, RJ ;
Balmain, A .
NATURE GENETICS, 2001, 29 (02) :117-129
[9]   Smad-dependent and Smad-independent pathways in TGF-β family signalling [J].
Derynck, R ;
Zhang, YE .
NATURE, 2003, 425 (6958) :577-584
[10]   Mechanisms of disease: the role of stem cells in the biology and treatment of gliomas [J].
Dietrich, Joerg ;
Imitola, Jaime ;
Kesari, Santosh .
NATURE CLINICAL PRACTICE ONCOLOGY, 2008, 5 (07) :393-404