期刊文献+

浙江台州地区使用伊立替康人群UGT1A1基因多态性相关性研究 被引量:2

Relevance Research of UGT1A1 Gene Polymorphism in Taizhou Area of Zhejiang Province Patients with Irinotecan Chemotherapy
原文传递
导出
摘要 目的研究浙江台州地区使用伊立替康(CPT-11)人群UGT1A1基因多态性和不良反应的相关性。方法以使用含CPT-11化疗的132例台州地区汉族肿瘤患者为研究对象,取其外周血提取基因组DNA,进行UGT1A1基因多态性检测。结果 132例以CPT-11为基础化疗方案的台州地区肿瘤患者中UGT1A1^*28 TA(6/6)野生型93例(70.45%),TA(6/7)杂合突变型共36例(27.27%),TA(7/7)纯合突变型仅3例(2.27%);UGT1A1^*6G/G野生型共97例(73.48%),G/A杂合突变型共35例(26.52%),未找到A/A纯合突变型。UGT1A1^*28非野生型(6/7+7/7)患者发生腹泻的概率显著高于野生型患者(P=0.040)。而粒细胞减少、血小板减少、血红蛋白减少与UGT1A1^*28基因多态性无显著性差异。迟发性腹泻、粒细胞减少、血小板减少、血红蛋白减少水平与UGT1A1^*6基因多态性无显著性差异。结论浙江台州地区UGT1A1基因突变频率较高,TA(6/6)野生型人群相比TA(6/7)和TA(7/7),CPT-11使用后的腹泻风险增加。建议浙江台州地区肿瘤患者使用CPT-11化疗前进行UGT1A1基因多态性检测,以预测患者对CPT-11的耐受性,保证化疗的顺利进行。 OBJECTIVE To investigate UGT1 A1 gene polymorphism and adverse relevance of irinotecan users in Taizhou, Zhejiang. METHODS Choose 132 Han nationality tumor patients treated with irinotecan-based chemotherapy in Taizhou. Take their peripheral blood to extract DNA for test of UGT1 A1 gene polymorphism. RESULTS Among 132 cancer patients in Taizhou collected to detect UGT1 A1 gene polymorphisms, the rates of wide type TA(6/6), heterozygous mutants TA(6/7), homozygous mutants TA(7/7) of UGT1 A1^*28 gene were 70.45%, 27.27%, 2.27%. The rates of UGT1 A1^*6 wide type G/G were 73.48% and heterozygous mutants of G/A were 26.52%. The incidence of diarrhea in UGT1 A1^*28 non-wild type patients(6/7+7/7) was significantly higher than that in wild type patients(P=0.040). There was no significant difference between UGT1 A1^*28 gene polymorphism and neutropenia, thrombocytopenia and hemoglobin reduction. There was no correlation between UGT1 A1^*6 gene polymorphism and delayed diarrhea, neutropenia, thrombocytopenia and hemoglobin reduction. CONCLUSION UGT1 A1 has a high frequency in Taizhou, Zhejiang. To TA(6/7) and TA(7/7) throng, there are obviously more diarrhea after using irinotecan during TA(6/6) wild-type throng. The study suggests that lung and colorectal cancer patients in Taizhou, Zhejiang, should do the test of UGT1 A1 gene promoter polymorphism before chemotherapy with irinotecan. It will assist predicting patients’ resistance so that it can adjust the dosage to help the smooth progress of chemotherapy.
作者 厉世笑 周鹏 LI Shixiao;ZHOU Peng(Taizhou Hospital of Zhejiang Province,Taizhou Enze Medical Center(Group),Department of Laboratory,Linhai 317000,China;Taizhou Hospital of Zhejiang Province,Taizhou Enze Medical Center(Group)Department of Pharmacy,Linhai 317000,China)
出处 《中国现代应用药学》 CAS CSCD 北大核心 2019年第19期2450-2453,共4页 Chinese Journal of Modern Applied Pharmacy
基金 台州市科技计划项目(16KY13)
关键词 伊立替康 UGT1A1 基因多态性 化疗 irinotecan UGT1A1 gene polymorphism chemotherapy
  • 相关文献

参考文献4

二级参考文献69

  • 1杨学宁,吴一龙.实体瘤治疗疗效评价标准——RECIST[J].循证医学,2004,4(2):85-90. 被引量:1469
  • 2Jian-Ming Xu,Yan Wang,Fei-Jiao Ge,Li Lin,Ze-Yuan Liu,Manish R Sharma.Severe irinotecan-induced toxicity in a patient with UGT1A1*28 and UGT1A1*6 polymorphisms[J].World Journal of Gastroenterology,2013,19(24):3899-3903. 被引量:14
  • 3Garcia-Carbonero R,Supko JG.Current perspectives on the clinical experience,pharmacology,and continued development of the camptothecins.Clin Cancer Res 2002; 8:641-661.
  • 4Ulukan H,Swaan PW.Camptothecins:a review of their chemotherapeutic potential.Drugs 2002; 62:2039-2057.
  • 5Saltz LB,Cox JV,Blanke C,Rosen LS,Fehrenbacher L,Moore MJ,Maroun JA,Ackland SP,Locker PK,Pirotta N,Elfring GL,Miller LL.Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer.Irinotecan Study Group.N Engl J Med 2000; 343:905-914.
  • 6Folprecht G,Kohne CH.The role of new agents in the treatment of colorectal cancer.Oncology 2004; 66:1-17.
  • 7Kawato Y,Aonuma M,Hirota Y,Kuga H,Sato K.Intracellular roles of SN-38,a metabolite of the camptothecin derivative CPT-11,in the antitumor effect of CPT-11.Cancer Res 1991; 51:4187-4191.
  • 8Vanhoefer U,Harstrick A,Achterrath W,Cao S,Seeber S,Rustum YM.Irinotecan in the treatment of colorectal cancer:clinical overview.J Clin Oncol 2001; 19:1501-1518.
  • 9Araki E,Ishikawa M,Iigo M,Koide T,Itabashi M,Hoshi A.Relationship between development of diarrhea and the concentration of SN-38,an active metabolite of CPT-11,in the intestine and the blood plasma of athymic mice following intraperitoneal administration of CPT-11.Jpn J Cancer Res 1993; 84:697-702.
  • 10Gupta E,Lestingi TM,Mick R,Ramirez J,Vokes EE,Ratain MJ.Metabolic fate of irinotecan in humans:correlation of glucuronidation with diarrhea.Cancer Res 1994; 54:3723-3725.

共引文献41

同被引文献19

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部