Islam Md Siddiqul, Islam Mohammad Safiqul, Parvin Salma, Ahmed Maizbah Uddin, Bin Sayeed Muhammad Shahdaat, Uddin Mir Muhammad Nasir, Hussain Syed Md Akram, Hasnat Abul
Department of Clinical Pharmacy and Pharmacology, Faculty of Pharmacy, University of Dhaka, Dhaka, 1000, Bangladesh.
Tumour Biol. 2015 Jul;36(7):5451-7. doi: 10.1007/s13277-015-3211-y. Epub 2015 Feb 13.
The most important cytotoxic drug namely, cyclophosphamide used in breast cancer along with epirubicin and 5-fluorouracil, is transported by ABCC transporters and detoxified by glutathione S-transferases (GSTs). The activities of these enzymes and transporters may vary in different population due to the presence of genetic polymorphisms. This study was aimed to evaluate the effects of GSTP1rs1695 and ABCC4rs9561778 polymorphisms on the response and toxicities produced by chemotherapy used in the treatment of Bangladeshi breast cancer patients. A total of 200 and 56 patients with invasive breast cancers were recruited from different public and private hospitals of Bangladesh of which 117 patients received neoadjuvant chemotherapy to examine the response as well as the toxicity, and another 139 patients received adjuvant chemotherapy to evaluate only the toxicity. Genetic polymorphisms of the mentioned genes were detected by using Polymerase Chain Reaction Restriction Fragment Length Polymorphism (PCR RFLP). Patients carrying AG and AG plus GG genotype of GSTP1rs1695 were more likely to have a good response, whereas no association of ABCC4rs9561778 was found with the chemotherapy response. Patients carrying GT and GT plus TT genotypes of ABCC4rs9561778 were found to be associated with anemia, neutropenia, leukopenia, and gastrointestinal toxicities when compared with GG genotype whereas no association was found with thrombocytopenia. GSTP1rs1695 was not associated with any type of toxicities investigated. Our result indicates that GSTP1rs1695 polymorphism was strongly associated with the response of chemotherapy, whereas ABCC4rs9561778 polymorphism was significantly related with chemotherapy-induced toxicities.
用于乳腺癌治疗的最重要的细胞毒性药物,即环磷酰胺,与表柔比星和5-氟尿嘧啶联合使用时,通过ABCC转运蛋白进行转运,并由谷胱甘肽S-转移酶(GSTs)进行解毒。由于基因多态性的存在,这些酶和转运蛋白的活性在不同人群中可能会有所不同。本研究旨在评估GSTP1 rs1695和ABCC4 rs9561778基因多态性对孟加拉国乳腺癌患者化疗反应及毒性的影响。从孟加拉国不同的公立和私立医院招募了总共200例和56例浸润性乳腺癌患者,其中117例患者接受新辅助化疗以检查反应及毒性,另外139例患者接受辅助化疗以仅评估毒性。使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测上述基因的基因多态性。携带GSTP1 rs1695的AG和AG加GG基因型的患者更有可能有良好的反应,而未发现ABCC4 rs9561778与化疗反应有关联。与GG基因型相比,携带ABCC4 rs9561778的GT和GT加TT基因型的患者被发现与贫血、中性粒细胞减少、白细胞减少和胃肠道毒性有关,而与血小板减少无关。GSTP1 rs1695与所研究的任何类型的毒性均无关联。我们的结果表明,GSTP1 rs1695基因多态性与化疗反应密切相关,而ABCC4 rs9561778基因多态性与化疗诱导的毒性显著相关。