Literature DB >> 28215024

Pharmacogenomics of platinum-based chemotherapy in non-small cell lung cancer: focusing on DNA repair systems.

Yi Xiong1, Bi-Yun Huang2, Ji-Ye Yin3,4.   

Abstract

Drug therapy for non-small cell lung cancer consists mainly of platinum-based chemotherapy regimens. However, toxicity, drug resistance, and high risk of death have been seen in the clinic, which means there is a need for optimizing the use of medications. Platinum resistance could be mediated by a series of DNA repair pathways, and therefore, these pathways should be taken into account for optimizing drug using. The goal of pharmacogenomics is to elucidate genetic factors, such as DNA repair genes, which might underlie drug efficacy and effectiveness, and to improve therapeutic effects or guide personalized therapy as well. Here, we reviewed the current knowledge of pharmacogenomic data on DNA repair systems and examined whether they could be further translated into the clinic with evidence-based perspectives.

Entities:  

Keywords:  Cisplatin; DNA repair pathway(s); Drug response; Single nucleotide polymorphism(s); Survival

Mesh:

Substances:

Year:  2017        PMID: 28215024     DOI: 10.1007/s12032-017-0905-6

Source DB:  PubMed          Journal:  Med Oncol        ISSN: 1357-0560            Impact factor:   3.064


  95 in total

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Journal:  Lung Cancer       Date:  2011-02       Impact factor: 5.705

2.  DNA repair gene polymorphism associated with sensitivity of lung cancer to therapy.

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Journal:  Med Oncol       Date:  2011-07-31       Impact factor: 3.064

3.  Correlation of MSH3 polymorphisms with response and survival in advanced non-small cell lung cancer patients treated with first-line platinum-based chemotherapy.

Authors:  X-L Xu; Y-L Yao; W-Z Xu; J-G Feng; W-M Mao
Journal:  Genet Mol Res       Date:  2015-04-15

Review 4.  Pharmacogenomics of platinum-based chemotherapy sensitivity in NSCLC: toward precision medicine.

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Journal:  Pharmacogenomics       Date:  2016-07-27       Impact factor: 2.533

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6.  Association of ERCC1-C118T and -C8092A polymorphisms with lung cancer risk and survival of advanced-stage non-small cell lung cancer patients receiving platinum-based chemotherapy: a pooled analysis based on 39 reports.

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Authors:  Penny A Jeggo; Markus Löbrich
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9.  ERCC1/BRCA1 expression and gene polymorphisms as prognostic and predictive factors in advanced NSCLC treated with or without cisplatin.

Authors:  M Tiseo; P Bordi; B Bortesi; L Boni; C Boni; E Baldini; F Grossi; F Recchia; F Zanelli; G Fontanini; N Naldi; N Campanini; C Azzoni; C Bordi; A Ardizzoni
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  16 in total

1.  Confused reference in the article entitle: pharmacogenomics of platinum-based chemotherapy in non-small cell lung cancer-focusing on DNA repair systems.

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3.  Sequential Whole Exome Sequencing Reveals Somatic Mutations Associated with Platinum Response in NSCLC.

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5.  Genetic Variations and Cisplatin Nephrotoxicity: A Systematic Review.

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6.  3-deazaneplanocin A protects against cisplatin-induced renal tubular cell apoptosis and acute kidney injury by restoration of E-cadherin expression.

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7.  Mitochondrial markers predict survival and progression in non-small cell lung cancer (NSCLC) patients: Use as companion diagnostics.

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9.  Effect of RIF1 on response of non-small-cell lung cancer patients to platinum-based chemotherapy by regulating MYC signaling pathway.

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10.  Traditional Chinese Medicine Integrated with Chemotherapy for Stage II-IIIA Patients with Non-Small-Cell Lung Cancer after Radical Surgery: A Retrospective Clinical Analysis with Small Sample Size.

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