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Relationship between MAPK1 gene polymorphism and gefitinib hepatotoxicity in NSCLC patients with activating EGFR mutations
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Wei FENG1, Xi CHEN2, Shao-xing GUAN1, Li ZHANG2, Min HUANG1, Xue-ding WANG1, *
Acta Pharmaceutica Sinica | 2018, 53(5) : 760 - 764
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Acta Pharmaceutica Sinica | 2018, 53(5): 760-764
ORIGINAL ARTICLES·Pharmacology
Relationship between MAPK1 gene polymorphism and gefitinib hepatotoxicity in NSCLC patients with activating EGFR mutations
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Wei FENG1, Xi CHEN2, Shao-xing GUAN1, Li ZHANG2, Min HUANG1, Xue-ding WANG1, *
Affiliations
  • 1. Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510060, China
  • 2. Cancer Centre, Sun Yat-sen University, Guangzhou 510060, China
Published: 2018-05-12 doi: 10.16438/j.0513-4870.2018-0048
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The hepatotoxicity of gefitinib is an important factor limiting its clinical application. In order to control the toxicity, we conducted this study to find the gene variation that can explain and predict the occurrence and severity of hepatotoxicity of gefitinib. Ninety patients with non-small cell lung cancer were included in the retrospective clinical study. Detailed hepatotoxicity induced by gefitinib and epidemiological characteristics were recorded. Twenty-six candidate single-nucleotide polymorphisms of molecular targets, metabolic enzymes, transporters and chemokines were genotyped by matrix-assisted laser desorption/ionization time-of-flight platform. Various confounding factors, such as age, gender and smoking status, were included in the follow-up analysis and variability in the extent of hepatotoxicity was best explained by a multivariate logistic regression model incorporating. The severity of hepatotoxicity was associated with mitogen-activated protein kinase 1 rs13515 (OR=9.467, P=0.074). The research about pharmacogenomic of gefitinib identified the determinants of the drug-induced liver injury. These findings provide a basis to design clinical trials targeting a particular toxicity of gefitinib or similarly targeted agents to benefit patients on long-term gefitinib treatment.

gefitinib  /  non-small cell lung cancer  /  liver toxicity  /  pharmacogenomics
Wei FENG, Xi CHEN, Shao-xing GUAN, Li ZHANG, Min HUANG, Xue-ding WANG. Relationship between MAPK1 gene polymorphism and gefitinib hepatotoxicity in NSCLC patients with activating EGFR mutations[J]. Acta Pharmaceutica Sinica, 2018 , 53 (5) : 760 -764 . DOI: 10.16438/j.0513-4870.2018-0048
Year 2018 volume 53 Issue 5
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doi: 10.16438/j.0513-4870.2018-0048
  • Receive Date:2018-01-12
  • Online Date:2026-01-15
  • Published:2018-05-12
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  • Received:2018-01-12
  • Revised:2018-02-22
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    1. Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510060, China
    2. Cancer Centre, Sun Yat-sen University, Guangzhou 510060, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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