Enhanced RegIV Expression Predicts the Intrinsic 5-Fluorouracil (5-FU) Resistance in Advanced Gastric Cancer

被引:24
作者
Ying, Li-Sha [1 ]
Yu, Jiang-Liu [1 ]
Lu, Xiao-Xiao [1 ]
Ling, Zhi-Qiang [1 ]
机构
[1] Zhejiang Prov Canc Hosp, Zhejiang Canc Ctr, Zhejiang Canc Res Inst, Hangzhou 310022, Zhejiang, Peoples R China
关键词
Gastric cancer; Regenerating islet-derived family; member; 4; (RegIV); 5-Fluorouracil; ATP-tumor chemosensitivity assay; Real-time reverse transcriptase-PCR; TUMOR CHEMOSENSITIVITY ASSAY; DRUG-RESISTANCE; ESOPHAGEAL CANCER; PROSTATE-CANCER; IV EXPRESSION; CHEMOTHERAPY; FAMILY; OVEREXPRESSION; IDENTIFICATION; SENSITIVITY;
D O I
10.1007/s10620-012-2381-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
RegIV, a member of the Regenerating (REG) gene family, may be a marker for the prediction of resistance to 5-fluorouracil (5-FU)-based chemotherapy. However, the relationship between the intrinsic drug resistance of gastric cancer (GC) cells to 5-FU used alone (single FU) or in multidrug therapeutic regimens (5-FU combinations) and RegIV expression has not been investigated. The patient cohort comprised 45 patients with primary GC. The chemoresistance of GC cells to therapeutic regimens consisting of single 5-FU or FU combinations was investigated using the ATP-tumor chemosensitivity assay. The level of RegIV mRNA transcripts was determined by real-time reverse transcriptase-PCR. RegIV expression was evaluated as a novel predictive biomarker for the intrinsic drug resistance of primary GC cells to single 5-FU or 5-FU combinations. Upregulation of RegIV mRNA transcripts was observed in 36 of the 45 tumor specimens and was positively correlated with the invasive depth of the tumor cells (p = 0.000), the clinical stages (p = 0.000) and the in vitro intrinsic drug resistance of primary GC cells to 5-FU (p = 0.000) or 5-FU combinations. RegIV mRNA transcript level was strongly associated with the intrinsic resistance of GC cells to single 5-FU or 5-FU combinations, suggesting that RegIV may play an important role in the intrinsic resistance of GC cells to 5-FU and that targeted therapy against the RegIV gene could be applied to overcome 5-FU resistance in the treatment of GC.
引用
收藏
页码:414 / 422
页数:9
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