Abstract
O(6)-Methylguanine-DNA methyltransferase (MGMT), a ubiquitous DNA repair protein, reverses mutagenic and cytotoxic effects of O(6)-alkylguanine in DNA induced by chemotherapeutic N-alkyl N-nitrosourea and procarbazine type drugs by dealkylating the adduct. MGMT expression is down-regulated by wild-type p53 (WTp53) in human tumor cells. Here we report that p53 sequesters the Sp1 transcription factor to prevent its binding to the cognate cis elements in the MGMT promoter and thus inhibits MGMT expression. Sp1 overexpression abrogated the inhibitory effect of p53 on the MGMT promoter activity in a dose-dependent manner. Stable interaction of Sp1 with WTp53 was observed in HCT116 cells. Moreover, WTp53 overexpression reduced the binding of the nuclear extract to the Sp1 consensus sequence, even though recombinant p53 alone did not bind to the same sequence. Taken together, these results suggest that sequestration of Sp1 could be one of the mechanisms by which p53 negatively regulates MGMT expression, thus enhancing sensitivity of tumor cells to O(6)-alkylguanine generating drugs.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents, Alkylating / pharmacology
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Colonic Neoplasms / enzymology
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Colonic Neoplasms / genetics
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Colonic Neoplasms / metabolism
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Consensus Sequence
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DNA Repair*
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Dacarbazine / analogs & derivatives
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Dacarbazine / pharmacology
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Down-Regulation
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Glioblastoma / drug therapy
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Glioblastoma / genetics
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Glioblastoma / metabolism
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HCT116 Cells
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Humans
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Lung Neoplasms / enzymology
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Lung Neoplasms / genetics
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Lung Neoplasms / metabolism
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O(6)-Methylguanine-DNA Methyltransferase / antagonists & inhibitors
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O(6)-Methylguanine-DNA Methyltransferase / biosynthesis
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O(6)-Methylguanine-DNA Methyltransferase / genetics
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O(6)-Methylguanine-DNA Methyltransferase / metabolism*
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Promoter Regions, Genetic
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Protein Binding
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Sp1 Transcription Factor / genetics
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Sp1 Transcription Factor / metabolism*
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Temozolomide
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Tumor Suppressor Protein p53 / biosynthesis
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Tumor Suppressor Protein p53 / deficiency
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Tumor Suppressor Protein p53 / genetics
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Tumor Suppressor Protein p53 / metabolism*
Substances
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Antineoplastic Agents, Alkylating
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Sp1 Transcription Factor
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TP53 protein, human
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Tumor Suppressor Protein p53
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Dacarbazine
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O(6)-Methylguanine-DNA Methyltransferase
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Temozolomide