What Makes Growth Factor Switch From Tumor Suppressor to Tumor Promoter?

Dihua Yu, M.D., Ph.D. Hubert L. & Olive Stringer Distinguished Chair in Basic Science Professor and Deputy Chair Department of Molecular and Cellular Oncology Co-Director, Center of Biological Pathways The Univ. Texas MD Anderson Cancer Center Houston, TX 77030MedicalResearch.com Interview with:
Dihua Yu, M.D., Ph.D.
Hubert L. & Olive Stringer Distinguished Chair in Basic Science
Professor and Deputy Chair
Department of Molecular and Cellular Oncology
Co-Director, Center of Biological Pathways
The Univ. Texas MD Anderson Cancer Center Houston, TX 77030

Medical Research: What is the background for this study?

Dr. Yu: Transforming growth factor β (TGF-β) functions as a tumor suppressor in premalignant cells but may also function as a metastasis promoter in cancer cells. This study aimed to understand how the growth factor makes this switch between tumor suppressor to tumor promoter.

Medical Research: What are the main findings?

Dr. Yu: We reported that 14-3-3ζ overexpression (14-3-3ζ+++) can switch TGF-β’s function from tumor suppressor to metastasis promoter by changing Smad partners. Specifically, 14-3-3ζ+++ led to destabilization of p53, a Smad determinant in pre-malignant cells, thus disrupting p53/Smad complex, and consequently inhibiting TGF-β-induced p21 expression and cytostatic function in non-malignant human mammary epithelial cells (HMECs). On the contrary, 14-3-3ζ+++ stabilized Gli2, a Smad partner in cancer cells, and Gli2 complexed with Smads to promote TGF-β-induced parathyroid hormone-related protein (PTHrP) expression, which enhanced breast cancer bone metastasis. Remarkably, both transcriptomic analyses and clinical pathology data indicated that 14-3-3ζ+++ is associated with the loss of TGF-β’s tumor suppressor function and the gain of its metastasis promoter function by changing contextual partners of Smads. Taken together, we have identified 14-3-3ζ as a novel molecular switch of TGF-β’s function by altering Smad partners from p53 in pre-malignant cells to Gli2 in cancer cells. The study provided important answers to the long-standing questions of how and when TGF-β switches its functional roles from a tumor suppressor to a metastasis promoter. The findings established a scientific base for a new strategy of selectively targeting TGF-β signaling in cancer by inhibiting the cancer-specific Smad partner without blocking TGF-β’s tumor suppressor function in normal tissues.

Medical Research: What should clinicians and patients take away from your report?

Dr. Yu: The crucial role of TGF-β in cancer and other diseases has motivated a lot of efforts on developing TGF-β-targeting therapeutics, some of which have been tested in the clinic (Akhurst and Hata, 2012). In limited phase I and II trials for treating cancers that generally overexpress TGF-β, some patients with late-stage cancers received a marginal benefit from TGF-β inhibitors (Bogdahn et al., 2011). A major obstacle for effective TGF-β-targeting therapies has been the complex nature and opposing roles of TGF-β in different stages of cancer development. Thus, understanding the molecular mechanism by which TGF-β switches its role could guide more effective TGF-β-targeting strategies. In this regard, our findings (see Figure 7) suggest that the TGF-β functional switch by 14-3-3ζ and the contextual changes of Smad partners could be utilized as biomarkers to aid in 1) selecting appropriate cancer patients who will benefit from TGF-β antagonists, and 2) determining optimal treatment timing when TGF-β-targeted therapy inhibits cancer.

Medical Research: What recommendations do you have for future research as a result of this study?

Dr. Yu:

1. Develop more specific, second generation drugs to selectively target the TGF-β signaling in cancer and metastasis without impeding TGF-β’s physiological functions in normal tissues.

2. Use biomarker-guided selection of patients who will most likely respond to second generation selective therapies to effectively target TGF-β signaling in the era of personalized medicine

Citation:

14-3-3ζ Turns TGF-β’s Function from Tumor Suppressor to Metastasis Promoter in Breast Cancer by Contextual Changes of Smad Partners from p53 to Gli2

Jia Xu Sunil Acharya Ozgur Sahin Qingling Zhang Yohei Sait, Jun Yao, Hai Wang, Ping Li , Lin Zhang Frank J. Lowery, Wen-Ling Kuo, Yi Xiao Joe Ensor, Aysegul A. Sahin, Xiang H.-F. Zhang, Mien-Chie Hung, Jitao David Zhang, Dihua Yu

Cancer Cell: Volume 27, Issue 2, 9 February 2015, Pages 177–192

[wysija_form id=”1″]

 

MedicalResearch.com Interview with:, & Dihua Yu, M.D., Ph.D. (2015). What Makes Growth Factor Switch From Tumor Suppressor to Tumor Promoter? MedicalResearch.com

Last Updated on March 1, 2015 by Marie Benz MD FAAD

Tags: