Cancer Research SABCS  Sign up for Cancer Research eTOC's
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

Cancer Research 68, 9107, November 15, 2008. doi: 10.1158/0008-5472.CAN-08-2556
© 2008 American Association for Cancer Research

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yang, L.
Right arrow Articles by Moses, H. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yang, L.
Right arrow Articles by Moses, H. L.
Related Collections
Right arrow Cellular Pathobiology: Proliferation, Senescence, and Death
Right arrow Cancer Immunology
Right arrow Cancer Immunology: Adaptive Immunity

Reviews

Transforming Growth Factor β: Tumor Suppressor or Promoter? Are Host Immune Cells the Answer?

Li Yang and Harold L. Moses

Department of Cancer Biology, the Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tenessee

Requests for reprints: Li Yang or Harold Moses, Vanderbilt-Ingram Cancer Center, 612 PRB, 2220 Pierce Avenue, Nashville, TN 37232. Phone: 615-936-1507; Fax: 615-936-1790; E-mail: li.yang{at}vanderbilt.edu or hal.moses{at}vanderbilt.edu.

Key Words: immune • TGFβ • tumor microenvironment

Therapies targeting transforming growth factor β (TGFβ) signaling using neutralizing antibodies and small molecular inhibitors are in multiple clinical trails. However, TGFβ is known to work as both a tumor suppressor and a tumor promoter, and current knowledge does not provide sufficient information on what factors mediate this switch in function and when this switch occurs. Recent advances in multiple disciplines suggest that immune cells from the tumor host may provide the answer. [Cancer Res 2008;68(22):9107–11]




This article has been cited by other articles:


Home page
DevelopmentHome page
K. Wharton and R. Derynck
TGF{beta} family signaling: novel insights in development and disease
Development, November 15, 2009; 136(22): 3691 - 3697.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
A. Moustakas and C.-H. Heldin
The regulation of TGF{beta} signal transduction
Development, November 15, 2009; 136(22): 3699 - 3714.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
S. L. Nishimura
Integrin-Mediated Transforming Growth Factor-{beta} Activation, a Potential Therapeutic Target in Fibrogenic Disorders
Am. J. Pathol., October 1, 2009; 175(4): 1362 - 1370.
[Abstract] [Full Text] [PDF]


Home page
aacredbookHome page
X. Li and N. A. Bhowmick
Stromal TGF-{beta} Responsiveness in the Initiation and Progression of Tumorigenesis
Am. Assoc. Cancer Res. Educ. Book, April 18, 2009; 2009(1): 143 - 147.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2008 by the American Association for Cancer Research.