Genetic polymorphisms as potential pharmacogenetic biomarkers for platinum-based chemotherapy in non-small cell lung cancer

被引:1
|
作者
Sito, Hilary [1 ]
Tan, Shing Cheng [1 ]
机构
[1] Univ Kebangsaan Malaysia, UKM Med Mol Biol Inst, Kuala Lumpur, Malaysia
关键词
Non-small cell Lung cancer; Platinum-based chemotherapy; Genetic biomarkers; Genetic testing; Pharmacogenetics; SINGLE-NUCLEOTIDE POLYMORPHISMS; S-TRANSFERASE P1; DNA-REPAIR GENE; COPPER TRANSPORTER CTR1; METHYLENETETRAHYDROFOLATE REDUCTASE MTHFR; GEMCITABINE-BASED CHEMOTHERAPY; ANTICANCER DRUG CISPLATIN; CYTIDINE DEAMINASE; CLINICAL-OUTCOMES; MESSENGER-RNA;
D O I
10.1007/s11033-023-08915-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Platinum-based chemotherapy (PBC) is a widely used treatment for various solid tumors, including non-small cell lung cancer (NSCLC). However, its efficacy is often compromised by the emergence of drug resistance in patients. There is growing evidence that genetic variations may influence the susceptibility of NSCLC patients to develop resistance to PBC. Here, we provide a comprehensive overview of the mechanisms underlying platinum drug resistance and highlight the important role that genetic polymorphisms play in this process. This paper discussed the genetic variants that regulate DNA repair, cellular movement, drug transport, metabolic processing, and immune response, with a focus on their effects on response to PBC. The potential applications of these genetic polymorphisms as predictive indicators in clinical practice are explored, as are the challenges associated with their implementation.
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页数:25
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