The overall goal of this Program Project is to translate recent advances in the understanding of the molecular pathogenesis of cancer and the mechanisms of programmed cell death (apoptosis) into new cancer treatments. This Program Project is a logical development of the scientific collaboration of a group of investigators with major interests in studying apoptotic mechanisms and restoring the cancer cell apoptotic pathway. These investigators have complementary expertise in the areas of clinical trial design, clinical trials in gene transfer, vector technology, experimental radiation research, biochemistry, molecular biology, tumor suppressor genes, cell biology, and animal models. The projects are (1) Induction of Radiation Sensitivity and Apoptosis in Human Cancer Cells By Restoration of Wildtype p53 Expression, (2) Fas/FasL Interations in p53/radiation-induced Apoptosis, and (3) Strategies for Cell Death Manipulation in Cancer. The Cores are (A) Administration, (B) Laboratory Services, and (C) Informatics. The Program combines a clinical trial with laboratory research projects. The Projects are highly integrated so that the research in one project will advance the goals of the other projects and so there will be a bidirectional flow of information to generate new hypotheses. The overall goal of the Program Project is to test the hypothesis that restoration of critical gene function in the cancer cell can mediate therapeutic effects. The major emphasis in the Program Project is on apoptosis-related genes. The therapeutic potential of current vectors will be optimized, apoptotic mechanisms and their interaction with ionizing radiation will be studied, and new gene targets with therapeutic potential will be identified. The studies included in the Program Project could lead to cancer treatments targeted to specific genetic lesions in the cancer cell, thus representing novel mechanisms of action that could complement existing therapies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
3P01CA078778-04S1
Application #
6597285
Study Section
Subcommittee G - Education (NCI)
Program Officer
Rosenfeld, Bobby
Project Start
1999-07-23
Project End
2004-04-30
Budget Start
2002-05-07
Budget End
2003-04-30
Support Year
4
Fiscal Year
2002
Total Cost
$43,500
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Surgery
Type
Other Domestic Higher Education
DUNS #
001910777
City
Houston
State
TX
Country
United States
Zip Code
77030
Pataer, Apar; Kalhor, Neda; Correa, Arlene M et al. (2012) Histopathologic response criteria predict survival of patients with resected lung cancer after neoadjuvant chemotherapy. J Thorac Oncol 7:825-32
Kadowaki, Yoshihiko; Chari, Nikhil S; Teo, Albert E K et al. (2011) PI3 Kinase inhibition on TRAIL-induced apoptosis correlates with androgen-sensitivity and p21 expression in prostate cancer cells. Apoptosis 16:627-35
Pataer, Abujiang; Swisher, Stephen G; Roth, Jack A et al. (2009) Inhibition of RNA-dependent protein kinase (PKR) leads to cancer cell death and increases chemosensitivity. Cancer Biol Ther 8:245-52
Pataer, Abujiang; Chada, Sunil; Roth, Jack A et al. (2008) Development of Ad-mda7/IL-24-resistant lung cancer cell lines. Cancer Biol Ther 7:103-8
Pataer, Abujiang; Hu, Wenxian; Xiaolin, Lu et al. (2008) Adenoviral endoplasmic reticulum-targeted mda-7/interleukin-24 vector enhances human cancer cell killing. Mol Cancer Ther 7:2528-35
Pataer, A; Bocangel, D; Chada, S et al. (2007) Enhancement of adenoviral MDA-7-mediated cell killing in human lung cancer cells by geldanamycin and its 17-allyl- amino-17-demethoxy analogue. Cancer Gene Ther 14:12-8
Peng, Henry H; Wu, Shuhong; Davis, John J et al. (2006) A rapid and efficient method for purification of recombinant adenovirus with arginine-glycine-aspartic acid-modified fibers. Anal Biochem 354:140-7
Pataer, A; Fanale, M A; Roth, J A et al. (2006) Induction of apoptosis in human lung cancer cells following treatment with amifostine and an adenoviral vector containing wild-type p53. Cancer Gene Ther 13:806-14
Li, Zhongkui; Niu, Jiangong; Uwagawa, Tadashi et al. (2005) Function of polo-like kinase 3 in NF-kappaB-mediated proapoptotic response. J Biol Chem 280:16843-50
Sclabas, Guido M; Fujioka, Shuichi; Schmidt, Christian et al. (2005) Overexpression of tropomysin-related kinase B in metastatic human pancreatic cancer cells. Clin Cancer Res 11:440-9

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