Abstract | AIM: METHODS: Human lung cancer cell model expressing antisense PKC alpha was established and characterized by gene transfection and immunoblotting. Northern blotting was used to analyze the expression of multiple drug resistance (mdr-1) gene and antisense PKC alpha mRNA. IC50 for some anticancer drugs in cultured cells were measured. RESULTS: Expression of antisense PKC alpha mRNA inhibited mdr-1 gene expression in lung cancer cells and improved sensitivity to anticancer drugs ( harringtonine, carboplatin, bleomycin A5, vincristine and doxorubicin) in lung cancer cells. IC50 for harringtonine, carboplatin, bleomycin A5, vincristine, and doxorubicin was decreased by 46.4%, 42.1%, 79%, 69.9%, and 61.6% respectively. CONCLUSION: PKC alpha plays an important regulation role of mdr-1 gene expression and drug sensitivity in human lung cancer cells.
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Authors | X Y Wang, H T Liu |
Journal | Zhongguo yao li xue bao = Acta pharmacologica Sinica
(Zhongguo Yao Li Xue Bao)
Vol. 19
Issue 3
Pg. 265-8
(May 1998)
ISSN: 0253-9756 [Print] China |
PMID | 10375741
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Isoenzymes
- RNA, Antisense
- PRKCA protein, human
- Protein Kinase C
- Protein Kinase C-alpha
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Topics |
- Adenocarcinoma
(genetics, metabolism, pathology)
- Antineoplastic Agents
(pharmacology)
- Drug Resistance, Multiple
- Gene Expression Regulation
- Genes, MDR
- Humans
- Isoenzymes
(biosynthesis)
- Lung Neoplasms
(genetics, metabolism, pathology)
- Protein Kinase C
(biosynthesis)
- Protein Kinase C-alpha
- RNA, Antisense
(biosynthesis)
- Tumor Cells, Cultured
(drug effects, metabolism)
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