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乳腺癌患者的基因多态性与对5-氟尿嘧啶、阿霉素和环磷酰胺化疗的反应

Genetic polymorphisms and response to 5-fluorouracil, doxorubicin and cyclophosphamide chemotherapy in breast cancer patients.

作者信息

Tecza Karolina, Pamula-Pilat Jolanta, Lanuszewska Joanna, Grzybowska Ewa

机构信息

Center for Translational Research and Molecular Biology of Cancer, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice Branch, Warsaw, Poland.

出版信息

Oncotarget. 2016 Oct 11;7(41):66790-66808. doi: 10.18632/oncotarget.11053.

Abstract

Clinical resistance to chemotherapy is one of the major problems in breast cancer treatment. In this study we analyzed possible impact of 22 polymorphic variants on the treatment response in 324 breast cancer patients. Selected genes were involved in FAC chemotherapy drugs transport (ABCB1, ABCC2, ABCG2, SLC22A16), metabolism (CYP1B1, CYP2C19, GSTT1, GSTM1, GSTP1, TYMS, MTHFR, DPYD), drug-induced damage repair (ERCC1, ERCC2, XRCC1) and involved in regulation of DNA damage response and cell cycle control (ATM, TP53).Apart from preexisting metastases three polymorphic variants were independent prognostic high risk factors of lack of response to FAC chemotherapy. Our results showed that the response to treatment depended of the variability in genes engaged in drugs' transport (ABCC2 c.-24C>T, ABCB1 p.Ser893Ala/Thr) and in DNA repair machinery (ERCC2 p.Lys751Gln). Furthermore, the growing number of high-risk genotypes was reflected in gradual increase in risk of the non-responsiveness to treatment- from OR 2.68 for presence of two genotypes to OR 9.93 for carriers of all three negative genotypes in the group of all patients. Similar gene-dosage effect was observed in the subgroup of TNBCs. Also, TFFS significantly shortened with the increasing number of high-risk genotypes, with median of 54.4 months for carriers of one variant, to 51.5 and 34.9 months for the carriers of two and three genotypes, respectively.Our results demonstrate that results of cancer treatment are the effect of many clinical and genetic factors. It seems that multifactorial polymorphic models could be a potentially useful tool in personalization of cancer therapies. The novelty in our model is the over representation of triple negative breast cancer (TNBC) patients among the carriers of all unfavorable polymorphic variants. This finding contributes to the elucidation of the mechanisms of drug resistance in this subgroup of breast cancer patients.

摘要

化疗临床耐药是乳腺癌治疗中的主要问题之一。在本研究中,我们分析了22个多态性变体对324例乳腺癌患者治疗反应的可能影响。所选基因参与氟尿嘧啶、多柔比星、环磷酰胺(FAC)化疗药物转运(ABCB1、ABCC2、ABCG2、SLC22A16)、代谢(CYP1B1、CYP2C19、GSTT1、GSTM1、GSTP1、TYMS、MTHFR、DPYD)、药物诱导损伤修复(ERCC1、ERCC2、XRCC1)以及参与DNA损伤反应调控和细胞周期控制(ATM、TP53)。除了已存在的转移灶外,三个多态性变体是对FAC化疗无反应的独立预后高危因素。我们的结果表明,治疗反应取决于参与药物转运的基因(ABCC2 c.-24C>T、ABCB1 p.Ser893Ala/Thr)和DNA修复机制(ERCC2 p.Lys751Gln)的变异性。此外,高危基因型数量的增加反映在治疗无反应风险的逐渐增加上——在所有患者组中,从两种基因型存在时的比值比(OR)2.68到所有三种阴性基因型携带者的OR 9.93。在三阴性乳腺癌(TNBC)亚组中观察到类似的基因剂量效应。此外,总无进展生存期(TFFS)随着高危基因型数量的增加而显著缩短,一种变体携带者的中位数为54.4个月,两种和三种基因型携带者分别为51.5个月和34.9个月。我们的结果表明,癌症治疗结果是多种临床和遗传因素的作用。似乎多因素多态性模型可能是癌症治疗个性化的潜在有用工具。我们模型的新颖之处在于,在所有不利多态性变体携带者中,三阴性乳腺癌(TNBC)患者的比例过高。这一发现有助于阐明该亚组乳腺癌患者的耐药机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e69/5341838/9dde73b60a62/oncotarget-07-66790-g001.jpg

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