GLUTATHIONE S TRANSFERASE MEDIATED MECHANISMS OF DRUG RESISTANCE
GLUTATHIONE S TRANSFERASE MEDIATED MECHANISMS OF DRUG RESISTANCE
批准号:
6239952
负责人:
Hassan Ahmad
金额:
$12.25万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-08-01 至 1998-07-31
关键词:
alkylating agents antineoplastics athymic mouse drug interactions drug metabolism drug resistance electrofocusing enzyme activity enzyme inhibitors glutathione transferase high performance liquid chromatography human tissue immunoaffinity chromatography ion exchange chromatography isozymes laboratory rabbit neoplastic cell protein structure function sulfonamides thin layer chromatography
中文摘要
各种抗癌药物的成功可能会受到严重限制,因为
英文摘要
Success of various anticancer drugs could be severely limited due to
acquired resistance against these drugs. Increasing body of evidence
strongly suggests that glutathione S-transferase (GSTs) might play a
crucial role in the development of drug resistance against alkylating
chemotherapeutic drugs. Over-expression of GST in may alklylating drug
resistant cells may suggest that these multi-functional enzymes provide
enhanced detoxification mechanisms and thereby reduce the cytotoxicity
of chemotherapeutic drugs. Inhibition of GSTs in some cells lines, has
been shown to at least partially reverse the resistance against
alkylating agents. Based on these and a number of other studies, it is
widely assumed that alkylating drugs are intracellularly inactivated
through GSH/GST-dependent metabolism, however, direct role of GST-
dependent drug detoxification in resistant cells in not proved.
Therefore, in the present studies we propose to purify, characterize and
compare the properties of GST isoenzyme(s) associated with the wild type
and drug resistant HS-Sultan myeloma and human small cell lung cancer
(NCI H-69) cells. We will also quantitate the efficiency for alkylating
agent conjugation by these isoenzymes in vitro as well as in the wild
type and drug resistant cells growth in culture, by isolating and
quantitating the drug-GSH conjugates. In addition, various sulfonamides
will be evaluated for their inhibitory effects on the cancer cell
associated GST isoenzymes. Finally, the most effective of the various
proposed sulfonamide inhibitors of GST, will be evaluated for
potentiation of alkylating agent cytotoxicity in the resistant cells as
well as in tumors grown in nude mice from the resistant cells. This will
be achieved by incubating the resistant cells or injecting the nude mice
(having tumors from resistant) cells) along with the alkylating drugs.
The results of these studies are expected to help delineate the role of
GST in alkylating agent drug resistance and will also provide invaluable
information in developing strategies for effective treatment of cancer.
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Mechanism of Anticarcinigenic Effects of Myristicin
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批准号:6804814
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项目类别:
-
资助金额:$20.57万
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财政年份:2004
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负责人:Hassan Ahmad
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依托单位:
GLUTATHIONE/GLUTATHIONE S TRANSFERASE MEDIATED MECHANISMS OF DRUG RESISTANCE
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批准号:6482461
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项目类别:
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资助金额:$6.61万
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财政年份:2001
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负责人:Hassan Ahmad
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依托单位:
GLUTATHIONE/GLUTATHIONE S TRANSFERASE MEDIATED MECHANISMS OF DRUG RESISTANCE
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批准号:6344851
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项目类别:
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资助金额:$14.19万
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财政年份:2000
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负责人:Hassan Ahmad
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依托单位:
GLUTATHIONE/GLUTATHIONE S TRANSFERASE MEDIATED MECHANISMS OF DRUG RESISTANCE
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批准号:6478806
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项目类别:
-
资助金额:$6.61万
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财政年份:2000
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负责人:Hassan Ahmad
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依托单位:
GLUTATHIONE/GLUTATHIONE S TRANSFERASE MEDIATED MECHANISMS OF DRUG RESISTANCE
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批准号:6216572
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项目类别:
-
资助金额:$14.19万
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财政年份:1999
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负责人:Hassan Ahmad
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依托单位:
GLUTATHIONE/GLUTATHIONE S TRANSFERASE MEDIATED MECHANISMS OF DRUG RESISTANCE
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批准号:6204099
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项目类别:
-
资助金额:$14.19万
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财政年份:1999
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负责人:Hassan Ahmad
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依托单位:
GLUTATHIONE/GLUTATHIONE S TRANSFERASE MEDIATED MECHANISMS OF DRUG RESISTANCE
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批准号:6107063
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项目类别:
-
资助金额:$14.19万
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财政年份:1998
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负责人:Hassan Ahmad
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依托单位:
PROTECTIVE MECHANISMS AGAINST CATARACTOGENESIS
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批准号:2164591
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项目类别:
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资助金额:$9.71万
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财政年份:1994
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负责人:Hassan Ahmad
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依托单位:
GLUTATHIONE S TRANSFERASE MEDIATED MECHANISMS OF DRUG RESISTANCE
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批准号:5211568
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:Hassan Ahmad
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依托单位:--
海外基金