{"title":"Genes Correlated with Gemcitabine Efficacy in Non-small Cell Lung Cancer","authors":"Chunhong Li, Meiyan Liu, Hailing Lu, Wei Liu, L. Cai, Xiaoqun Dong","doi":"10.4172/1948-5956.1000540","DOIUrl":null,"url":null,"abstract":"Objective: Gemcitabine in combination with platinum improves survival of patients with non-small cell lung cancer (NSCLC). The purpose of the study was to explore genes related to gemcitabine efficacy. Methods: The sensitivity of NSCLC cell lines to anticancer drugs was tested via MTT assay. Gene expression analysis was performed by cDNA microarray, and qRT-PCR was used for verification of the microarray results on highly sensitive genes. Fluorouracil (5-Fu) was used as the negative control of gemcitabine. Results: Gemcitabine-related and fluorouracil-related genes were pooled into different clusters. Genes negatively related to 5-Fu sensitivity were positively related to gemcitabine efficacy. Metallothionein, Cathepsin B, TIMP1 and Galectin-1 genes which were resisted to certain anticancer drugs were sensitive to gemcitabine (P<0.05). Conclusion: Metallothionein, Cathepsin B, TIMP1 and Galectin-1 can be considered as the predictors for gemcitabine sensitivity.","PeriodicalId":15170,"journal":{"name":"Journal of Cancer Science & Therapy","volume":"19a 1","pages":"169-172"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cancer Science & Therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/1948-5956.1000540","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Objective: Gemcitabine in combination with platinum improves survival of patients with non-small cell lung cancer (NSCLC). The purpose of the study was to explore genes related to gemcitabine efficacy. Methods: The sensitivity of NSCLC cell lines to anticancer drugs was tested via MTT assay. Gene expression analysis was performed by cDNA microarray, and qRT-PCR was used for verification of the microarray results on highly sensitive genes. Fluorouracil (5-Fu) was used as the negative control of gemcitabine. Results: Gemcitabine-related and fluorouracil-related genes were pooled into different clusters. Genes negatively related to 5-Fu sensitivity were positively related to gemcitabine efficacy. Metallothionein, Cathepsin B, TIMP1 and Galectin-1 genes which were resisted to certain anticancer drugs were sensitive to gemcitabine (P<0.05). Conclusion: Metallothionein, Cathepsin B, TIMP1 and Galectin-1 can be considered as the predictors for gemcitabine sensitivity.