课题基金 / 基金详情

RESTORATION OF APOPTOSIS IN CANCER

RESTORATION OF APOPTOSIS IN CANCER
癌症细胞凋亡的恢复
批准号:
6751382
负责人:
Jack Roth
金额:
$0.17万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-07-23 至 2004-04-30

项目摘要

项目成果

Jack Roth的其他基金

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中文摘要
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英文摘要
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.
期刊论文(61)
专著(0)
科研奖励(0)
会议论文
Enhancement of adenoviral MDA-7-mediated cell killing in human lung cancer cells by geldanamycin and its 17-allyl- amino-17-demethoxy analogue.
格尔德霉素及其 17-烯丙基-氨基-17-去甲氧基类似物增强腺病毒 MDA-7 介导的人肺癌细胞杀伤作用。
DOI: 10.1038/sj.cgt.7700989
发表时间: 2007
期刊: Cancer gene therapy
影响因子: 6.4
作者: [Pataer,A, Bocangel,D, Chada,S, Roth,JA, Hunt,KK, Swisher,SG]
通讯作者: Swisher,SG
DOI: 10.1016/j.ymthe.2004.01.007
发表时间: 2004-03
期刊: Molecular therapy : the journal of the American Society of Gene Therapy
影响因子: --
作者: [Isao Ito;Tomoyuki Saeki;I. Mohuiddin;Yuji Saito;C. Branch;A. Vaporciyan;J. Roth;R. Ramesh]
通讯作者: Isao Ito;Tomoyuki Saeki;I. Mohuiddin;Yuji Saito;C. Branch;A. Vaporciyan;J. Roth;R. Ramesh
DOI: 10.1158/1535-7163.985.3.8
发表时间: 2004-08
期刊: Molecular cancer therapeutics
影响因子: 5.7
作者: [A. Munshi;J. Kurland;T. Nishikawa;P. Chiao;M. Andreeff;R. Meyn]
通讯作者: A. Munshi;J. Kurland;T. Nishikawa;P. Chiao;M. Andreeff;R. Meyn
P53 gene replacement for cancer--interactions with DNA damaging agents.
P53 基因替换治疗癌症——与 DNA 损伤剂的相互作用。
DOI: 10.1080/02841860152619160
发表时间: 2001
期刊: Acta oncologica (Stockholm, Sweden)
影响因子: --
作者: [Roth,JA, Grammer,SF, Swisher,SG, Komaki,R, Nemunaitis,J, Merritt,J, Meyn,RE]
通讯作者: Meyn,RE
28
    Administrative Core
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    Administrative Core
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    海外基金