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[1]孙建伟,陈瑶,刘青青,等.MDR1基因多态性与乳腺癌的相关性研究[J].慢性病学杂志,2016,(01):48-51.
 SUN Jian-wei,CHEN Yao,LIU Qing-qing,et al.Relationship between MDR1gene polymorphism and breast carcinoma[J].,2016,(01):48-51.
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MDR1基因多态性与乳腺癌的相关性研究(PDF)

《慢性病学杂志》[ISSN:1674-8166/CN:11-5900/R]

卷:
期数:
2016年01期
页码:
48-51
栏目:
论著
出版日期:
2016-02-15

文章信息/Info

Title:
Relationship between MDR1gene polymorphism and breast carcinoma
作者:
孙建伟1陈瑶2刘青青2贾玲1陈居敏1刘春生1纳志明1
云南省第一人民医院/昆明理工大学附属医院(1.乳腺甲状腺肿瘤科;2.药学科),昆明 650034
Author(s):
SUN Jian-weiCHEN YaoLIU Qing-qingJIA LingCHEN Ju-minLIU Chun-shengNA Zhi-ming
FirstPeople’s HospitalofYunnanProvince,Kunming,Yunnan650034, China Correspondingauthor:SUNJian-wei,E-mail:sunjianwei0630@163.com
关键词:
乳腺肿瘤多药耐药基因1多态性
Keywords:
Breast cancer MDR1 Polymorphisms
分类号:
R737.9
DOI:
-
摘要:
目的 探讨MDR1基因多态性与其在乳腺癌患者癌组织中表达水平、药物治疗反应及预后关系。方 法 选取153例乳腺癌组织及40例配对癌旁组织、20例乳腺纤维腺瘤组织,利用PCR-RFLP技术检测 MDR1 exon12(1236)、exon21(2677)、exon26(3435) 3 个位点的多态性,以RT-qPCR 技术对MDR1 mRNA进行相对定量,分析不同基因型患者对药物治疗的反应及预后。结果 153例乳腺癌病例中有65例 有MDR1基因扩增,总体扩增率为42.5%,表达值范围0~1.42×10 5基因拷贝/μl。在13例有效病例中,基 因型CC型占11例、GT型占2例,而TT型则全部无效,TT型与其他型差异有统计学意义(P= 0.031 7),其中C3435T的TT化疗疗效显著低于CC和GT型(P=0.006 5)。结论 MDR1基因在乳腺癌 组织中的高表达,其SNP位点基因型可作为药物治疗反应及预后的预测因子。
Abstract:
Objective To investigate the relationship between MDR1 gene polymorphism, response to drug treatment and prognosis of breast carcinoma patients. Methods A total of153 cases of breast can-cer tissues, 40 cases matched adjacent tissues, and 20 cases of breast fibroadenoma tissue were studied. PCR-RFLP technique was used to detect MDR1 exon12 (1236), exon21 (2677), exon26 (3435), 3 sin-gle nucleotide polymorphic (SNP) loci. RT-qPCR technique was used to detect relative expression level of MDR1 mRNA. Based on the results, response to drug treatment and prognosis of different geno-types were compared. Results Among the153 cases of breast cancer, MDR1 gene amplification was successful in 65 cases, with an overall amplification rate of 42.5%. Expression values ranged from0 to 1.42×10 5 gene copies/μl. Among the 13 cases of effective cases, genotype CC accounted for 11 cases, GT accounted for2 cases. Genotype TT were all invalid. There is a significant difference between the TT and other types (P=0.031 7). The chemotherapy effectiveness in the C3 435T type is signifi-cantly lower than those in the CC and GT type (P=0.006 5). Conclusions The expression level of MDR1 gene in breast cancer, and the gene polymorphism can be predictors of drug response and prog-nosis in chemotherapy treatment.

参考文献/References:

[1] Shabbit JA, Mayer LD. P-glycoprotein modulates ceramide? mediated sensitivity of human breast cancer [J]. Mol Cancer Ther,2002,1(3):205-213.
[2] Noguchi S. Predicitive factors for response to docetaxel in hu? man breastcancer[J].CancerSci,2006,97(9):813-820.
[3] Taheril M, Mahjoubi1 F, Omranipour R. Effect of MDR1 polymorphism on multidrug resistance expression in breast can? cerpatients [J]. Genetand MolRes,2010,9(1):34-40.
[4] Mutoh K, Mitsuhashi J, Kimura Y, et al. A T3587G germ-line mutation of the MDR1gene encodes a nonfunctional P-glycoprotein [J].MolCancerTher,2006,5(4):877-884.
[5] 王健,唐金海,赵建华.紫杉醇药物代谢酶和转运体的遗传多态性与乳腺癌化疗反应[J].分子诊断与治疗杂志,2010,2(1):63-68.
[6] Hoffimeyers S, Burk O, von Richter O,etal.Functionalpoly? morphisms of the human multidrug- resistance gene:multiple sequence variations and correlation of one allele with P-glyco? protein expression and activity in vivo [J]. Pro Natl Acad Sci USA,2000,97(7):3473-3478.
[7] Cizmarikova M, Wagnerova M, Schonova L, et al. MDR1 (C3435T) polymorphism: relation to the risk of breast cancer and therapeutic outcome [J]. Pharmacogenomics J,2009,10(1): 62–69.
[8] Gerloff T, Schaefer M, Johne A, et al. MDR1genotypes do not influence the absorption of a single oral dose of1mg digox? in in healthy white males [J]. Br J Clin Pharmacol, 2002,54(6): 610–616.
[9] Tsutomu N, ToshiyukiS, MasanoriH,etal.Effectofthe mu? tation (C3435T) at exon26of the MDR1gene on expression level of MDR1messenger ribonucleic acid in duodenal entero? cytes of healthy Japanese subjects [J]. Clin Pharmacol Ther, 2002,71(4):297–303.
[10] 刘学敏,王树生.MDR1基因多态性与其在乳腺癌患者中表达 水平的关系[J].现代肿瘤学,2013,21(2):319-321.

备注/Memo

备注/Memo:
作者简介:孙建伟,硕士,副主任医师,研究方向:乳 腺肿瘤的基础与临床研究 通信作者:孙建伟,E-mail: sunjianwei0630@163.com
更新日期/Last Update: 2016-03-18