Department of Oncology, Krishna Vishwa Vidyapeeth "Deemed to be University", Taluka-Karad, Dist- Satara, Pin-415 539, Maharashtra, India.
Department of Molecular Biology & Genetics,Krishna Vishwa Vidyapeeth "Deemed to be University", Taluka-Karad, Dist- Satara, Pin-415 539, Maharashtra, India.
Asian Pac J Cancer Prev. 2024 May 1;25(5):1567-1577. doi: 10.31557/APJCP.2024.25.5.1567.
ATP Binding Cassette Transporters (ABCB1) gene plays an important role in transport of different metabolites and anticancer drugs across the cell membrane. There is lack of knowledge on ABCB1 gene polymorphism and its correlation with Adriamycin or paclitaxel based chemotherapy induced toxicity in breast cancer patients. Therefore in this study, we explored the correlation of ABCB1 polymorphisms gene on response and toxicity in adriamycin and paclitaxel based chemotherapy in breast cancer patients from Indian population.
Two hundred BC patients receiving Adriamycin and paclitaxel chemotherapy were enrolled in this study and chemotherapy induced hematological and non-hematological toxicity reactions were noted. The polymorphisms in ABCB1 gene (C1236T, C3435T) were studied by PCR and RFLP analysis.
The univariate logistic regression analysis showed statistically significant negative association with protective effects of ABCB1 (C3435T) polymorphism with heterozygous genotype (OR=0.34, 95% CI: 0.13-0.89; p=0.027), homozygous variant genotype (OR=0.31, 95% CI: 0.10-0.99; p=0.049) and combined C/T+T/T genotypes (OR=0.33, 95% CI: 0.13-0.79; p=0.013) in relation with severe toxicity of chemotherapy induced nausea and vomiting in breast cancer patients treated with Adriamycin chemotherapy. The 3435 C>T polymorphism of ABCB1 gene with heterozygous C/T genotype showed significantly negative association (OR=0.37, 95% CI: 0.14-0.96; p=0.042) with peripheral neuropathy in patients treated primarily with paclitaxel thereafter Adriamycin.
The findings obtained from this study revealed significant association of ABCB1 3435 C>T polymorphisms with non-hematological toxicity in response to adriamycin and paclitaxel based chemotherapy.
三磷酸腺苷结合盒转运蛋白(ABCB1)基因在不同代谢物和抗癌药物穿过细胞膜的运输中起着重要作用。关于 ABCB1 基因多态性及其与乳腺癌患者阿霉素或紫杉醇为基础的化疗诱导毒性的相关性知之甚少。因此,在这项研究中,我们探讨了印度人群中 ABCB1 基因多态性与阿霉素和紫杉醇为基础的化疗反应和毒性的相关性。
本研究纳入了 200 名接受阿霉素和紫杉醇化疗的乳腺癌患者,并观察了化疗引起的血液学和非血液学毒性反应。通过 PCR 和 RFLP 分析研究了 ABCB1 基因(C1236T、C3435T)的多态性。
单因素 logistic 回归分析显示,ABCB1(C3435T)多态性的杂合基因型(OR=0.34,95%CI:0.13-0.89;p=0.027)、纯合变异基因型(OR=0.31,95%CI:0.10-0.99;p=0.049)和 C/T+T/T 基因型(OR=0.33,95%CI:0.13-0.79;p=0.013)与乳腺癌患者阿霉素化疗所致严重恶心呕吐毒性有统计学显著的保护作用负相关。ABCB1 基因 3435C>T 多态性的杂合 C/T 基因型与紫杉醇后阿霉素主要治疗的患者的周围神经病变呈显著负相关(OR=0.37,95%CI:0.14-0.96;p=0.042)。
本研究结果表明,ABCB1 3435C>T 多态性与阿霉素和紫杉醇为基础的化疗的非血液学毒性反应有显著相关性。