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2015 Fiscal Year Final Research Report

Differential proteome analysis identifies TGF-beta related pro-metastatic proteins in a 4T1 murine breast cancer model

Research Project

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Project/Area Number 25871241
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Tumor biology
Genome biology
Research InstitutionOsaka City University

Principal Investigator

Matsubara, Sato Misako (佐藤三佐子)  大阪市立大学, 大学院医学研究科, 特任助教 (00635120)

Project Period (FY) 2013-04-01 – 2016-03-31
KeywordsTGF-beta / Proteomics / eIF signaling / metastatic mouse model / Breast cancer
Outline of Final Research Achievements

Although TGF-β antagonists have been proposed as anti-metastatic therapies for patients with advanced stage cancer, how TGF-β mediates metastasis-promoting effects is poorly understood. In the present study, we found that systemic administration of the TGF-β receptor kinase inhibitor, SB-431542, significantly inhibited lung metastasis from transplanted 4T1 mammary tumors in Balb/c mice. The differentially expressed proteins in the comparison of lung metastases from SB-431542 treated and control vehicle-treated groups were analyzed by proteomics analysis. Our proteomic approach newly identified eIF pathway proteins as novel potential mediators of TGF-β tumor-promoting activity.

Free Research Field

分子生物学

URL: 

Published: 2017-05-10  

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