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消化道肿瘤MDR1基因和P-糖蛋白的表达与化疗药物耐药的关系 被引量:9

The correlations between the expression of MDR1 gene and P-glycoprotein and chemotherapy drug resistance of gastrointestinal tumor
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摘要 目的探讨消化道肿瘤多药耐药基因MDR1基因和P-糖蛋白(P-gp)的表达与肿瘤化疗药物耐药之间的关系。方法选择72例消化道肿瘤患者的手术标本,采用荧光定量PCR检测MDR1 mRNA表达量,ELISA法检测P-gp表达水平,并与ATP-TCA化疗药物敏感性试验结果作对照。结果 72份消化道肿瘤组织中,MDR1 mRNA阳性表达率为75%,P-gp阳性表达率为67%。72份消化道肿瘤组织中,对10种化疗药物均不敏感的有12份,对1种化疗药物敏感的有15份,对2种化疗药物敏感的9份,对3种化疗药物敏感的有9份,对5种化疗药物敏感的有15份,对8种化疗药物敏感的有9份,对所有化疗药物均敏感的有3份。消化道肿瘤MDR1mRNA、P-gp的阳性表达率与其对化疗药物敏感程度呈负相关(r s值分别为-0.672、-0.715,均P<0.05)。结论 MDR1基因、P-gp表达与肿瘤耐药性相关,MDR1基因、P-gp阳性表达提示患者可能对化疗药物存在获得性耐药。 Objective To investigate the correlations between the expression of muhidrug resistance gene 1 ( MDR1 ) gene and P - glyeoprotein ( P - gp) and chemotherapy drug resistance of gastrointestinal (GI) tumor. Methods The expression of MDR1 mRNA and P - gp in 72 patients with GI cancer was measured by RT - PCR and ELISA. The chemotherapy drug sensitivity test was also conducted for eorrelaion analysis. Results The positive rates of MDR1 and P -gp in GI tumor tissue were 75% and 67%, respectively. There were 12 eases insensitive to 10 chemotherapy drugs; while singledrug, 2 -drug, 3 -drug, 5 -drug, 8 -drug and all- drug sensitive were revealed in 15, 9, 9, 15, 9 and 3 eases, respectively. The positive expression of MDR1 and P - gp was significantly negatively correlated with the sensitivity to chemotherapy in GI cancer ( rs = - 0. 672 and - 0. 715, P 〈 0. 05 ). Conclusion The expression of MDR1 and P - gp is correlated to the drug resistance of GI tumor, which indicates functional linkage of drug resistanee.
出处 《广东医学》 CAS CSCD 北大核心 2013年第20期3120-3123,共4页 Guangdong Medical Journal
基金 广东省自然科学基金面上项目(编号:10151031701000009)
关键词 消化道肿瘤 MDR1基因 P-糖蛋白 ATP-TCA gastrointestinal tumor MDR1 gene P - glyeoprotein ATP - TCA
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  • 1Gottesman MM. Mechanisms of cancer drug resistance. Annu Rev Med 2002; 53: 615-27.
  • 2Szakacs G, Paterson JK, Ludwig JA, Booth-Genthe C, Gottesman MM. Targeting multidrug resistance in cancer. Nat Rev Drug Discov 2006; 5: 219-34.
  • 3Fujita T, Washio K, Takabatake D, Takahashi H, Yoshitomi S, Tsukuda K, et al. Proteasome inhibitors can alter the signaling pathways and attenuate the P-glycoprotein-mediated multidrug resistance. Int J Cancer 2005; 117: 670-82.
  • 4Limtrakul P, Khantamat O, Pintha K. Inhibition of P-glycoprotein activity and reversal of cancer multidrug resistance by Momordica charantia extract. Cancer Chemother Pharmacol 2004; 54: 525-30.
  • 5Pitchakarn P, Ohnuma S, Pintha K, Pompimon W, Ambudkar SV, Limtrakul P. Kuguacin J isolated from Momordica charantia leaves inhibits P-glycoprotein (ABCB1)-mediated multidrug resistance. J Nutr Biochem 2012; 23: 76-84.
  • 6Chanmahasathien W, Ampasavate C, Greger H, Limtrakul P. Stemona alkaloids, from traditional Thai medicine, increase chemosensitivity via P-glycoprotein-mediated multidrug resistance. Phytomedicine 2011; 18: 199-204.
  • 7Romiti N, Tongiani R, Cervelli F, Chieli E. Effects of curcumin on P-glycoprotein in primary cultures of rat hepatocytes. Life Sci 1998; 62: 2349-58.
  • 8Anuchapreeda S, Leechanachai P, Smith MM, Ambudkar SV, Limtrakul PN. Modulation of P-glycoprotein expression and function by curcumin in multidrug-resistant human KB cells. Biochem Pharmacol 2002; 64: 573-82.
  • 9Singh S, Khar A. Biological effects of curcumin and its role in cancer chemoprevention and therapy. Anticancer Agents Med Chem 2006; 6: 259-70.
  • 10Chearwae W, Anuchapreeda S, Nandigama K, Ambudkar SV, Limtrakul P. Biochemical mechanism of modulation of human P-glycoprotein (ABCB1) by curcumin I, II, and III purified from Turmeric powder. Bio- chem Pharmacol 2004; 68" 2043-52.

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