Abstract
DNA repair capacity (DRC) is correlated with sensitivity of cancer cells toward platinum-based chemotherapy. We hypothesize that genetic polymorphisms in DNA repair gene XPA (xeroderma pigmentosum group A) and XPG (xeroderma pigmentosum group G) (ERCC5, excision repair cross-complementation group 5), which result in inter-individual differences in DNA repair efficiency, may predict clinical response to platinum agents in advanced non-small cell lung cancer (NSCLC) patients. In this study, we find that the Aright curved arrow G change of XPA A23G polymorphism significantly increased response to platinum-based chemotherapy. Polymorphism in XPG His46His was associated with a decreased treatment response, but was not statistically significant.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Aged, 80 and over
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Carboplatin / administration & dosage
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Carcinoma, Non-Small-Cell Lung / drug therapy*
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Carcinoma, Non-Small-Cell Lung / genetics
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Carcinoma, Non-Small-Cell Lung / pathology
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Cisplatin / administration & dosage
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DNA-Binding Proteins / genetics
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Deoxycytidine / administration & dosage
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Deoxycytidine / analogs & derivatives
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Docetaxel
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Endonucleases / genetics
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Female
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Gemcitabine
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Gene Frequency
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Genotype
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Humans
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Logistic Models
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Lung Neoplasms / drug therapy*
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Lung Neoplasms / genetics
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Lung Neoplasms / pathology
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Male
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Middle Aged
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Nuclear Proteins / genetics
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Paclitaxel / administration & dosage
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Polymorphism, Single Nucleotide*
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Taxoids / administration & dosage
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Transcription Factors / genetics
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Treatment Outcome
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Vinblastine / administration & dosage
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Vinblastine / analogs & derivatives
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Vinorelbine
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Xeroderma Pigmentosum Group A Protein / genetics*
Substances
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DNA excision repair protein ERCC-5
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DNA-Binding Proteins
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Nuclear Proteins
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Taxoids
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Transcription Factors
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XPA protein, human
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Xeroderma Pigmentosum Group A Protein
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Deoxycytidine
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Docetaxel
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Vinblastine
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Carboplatin
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Endonucleases
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Paclitaxel
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Cisplatin
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Vinorelbine
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Gemcitabine