TGFalpha is produced as a biologically active, high molecular weight integral membrane glycoprotein that undergoes complex processing to its mature 5.6kd form. We have shown that TGFalpha is produced by normal and transformed epithelial cells. While its precise role in neoplasia is unknown, we have recently demonstrated that overproduction of TGFalpha targeted to the mammary gland in transgenic mice leads to mammary carcinoma. In this model, however, events in addition to overexpression of TGFalpha are required for the malignant phenotype. By use of polyclonal antibodies that we have generated to different regions of the proTGFalpha molecule, we propose to fully characterize its production and processing in representative normal and transformed epithelial cell and tissues. In addition, we propose to identify likely second events that accompany the malignant phenotype in the mouse mammary transgenic model. Finally in transgenic models in which TGFalpha is overexpressed in the colon, we propose to test the hypothesis that TGFalpha acts as a tumor promoter. These studies are likely to provide important new understanding into the role of TGFalpha in the development of two commonly encountered human malignancies, mammary and colonic neoplasia.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA046413-06
Application #
3189671
Study Section
Metabolic Pathology Study Section (MEP)
Project Start
1988-05-01
Project End
1996-04-30
Budget Start
1993-05-01
Budget End
1994-04-30
Support Year
6
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Herring, Charles A; Banerjee, Amrita; McKinley, Eliot T et al. (2018) Unsupervised Trajectory Analysis of Single-Cell RNA-Seq and Imaging Data Reveals Alternative Tuft Cell Origins in the Gut. Cell Syst 6:37-51.e9
Schulte, Michael L; Fu, Allie; Zhao, Ping et al. (2018) Pharmacological blockade of ASCT2-dependent glutamine transport leads to antitumor efficacy in preclinical models. Nat Med 24:194-202
Banerjee, Amrita; McKinley, Eliot T; von Moltke, Jakob et al. (2018) Interpreting heterogeneity in intestinal tuft cell structure and function. J Clin Invest 128:1711-1719
Choi, Eunyoung; Lantz, Tyler L; Vlacich, Gregory et al. (2018) Lrig1+ gastric isthmal progenitor cells restore normal gastric lineage cells during damage recovery in adult mouse stomach. Gut 67:1595-1605
Yang, Yu-Ping; Ma, Haiting; Starchenko, Alina et al. (2017) A Chimeric Egfr Protein Reporter Mouse Reveals Egfr Localization and Trafficking In Vivo. Cell Rep 19:1257-1267
Wang, Jing; Mouradov, Dmitri; Wang, Xiaojing et al. (2017) Colorectal Cancer Cell Line Proteomes Are Representative of Primary Tumors and Predict Drug Sensitivity. Gastroenterology 153:1082-1095
Starchenko, Alina; Graves-Deal, Ramona; Yang, Yu-Ping et al. (2017) Clustering of integrin ?5 at the lateral membrane restores epithelial polarity in invasive colorectal cancer cells. Mol Biol Cell 28:1288-1300
Lu, Yuanyuan; Zhao, Xiaodi; Liu, Qi et al. (2017) lncRNA MIR100HG-derived miR-100 and miR-125b mediate cetuximab resistance via Wnt/?-catenin signaling. Nat Med 23:1331-1341
Short, Sarah P; Kondo, Jumpei; Smalley-Freed, Whitney G et al. (2017) p120-Catenin is an obligate haploinsufficient tumor suppressor in intestinal neoplasia. J Clin Invest 127:4462-4476
Li, Cunxi; Singh, Bhuminder; Graves-Deal, Ramona et al. (2017) Three-dimensional culture system identifies a new mode of cetuximab resistance and disease-relevant genes in colorectal cancer. Proc Natl Acad Sci U S A 114:E2852-E2861

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