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遗传 3'UTR 变异和临床因素显著影响乳腺癌患者的生存预测和临床反应。

Genetic 3'UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients.

机构信息

Department of Genetic and Molecular Diagnostics of Cancer, Center for Translational Research and Molecular Biology of Cancer, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice, Poland.

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

出版信息

Sci Rep. 2020 Mar 31;10(1):5736. doi: 10.1038/s41598-020-62662-z.

Abstract

The study describes a relationship between the 3'UTR variants, clinicopathological parameters and response to chemotherapy. We analyzed 33 germline polymorphisms in 3'UTRs of ADME genes in 305 breast cancer women treated with FAC regime. Clinical endpoints of this study were: overall survival (OS), progression-free survival (PFS), recurrence-free survival (RFS) and overall response defined as treatment failure-free survival (TFFS). The shortened OS was connected with the presence of NR1/2 rs3732359 AA, SLC22A16 rs7756222 CC, as well as SLC22A16 rs9487402 allele G and clinical factors belonging to TNM classification: tumor size >1 cm, nodal involvement and presence of metastases. PFS was related to two polymorphisms PGR rs1824125 GG, PGR rs12224560 CC and SLC22A16 rs7756222 CC as well as preexisting metastases. The RFS was shortened due to the DPYD rs291593 CC, AKR1C3 rs3209896 AG and negative expression of PGR. The presence of ALDH5A1 rs1054899 allele A, lack of pre-chemotherapy surgery and negative status of PGR correlated with worse treatment response. The germline variants commonly present in the population are important factors determining the response to treatment. We observed the effect of the accumulation of genetic and clinical factors on poor survival prognosis and overall treatment response.

摘要

本研究描述了 3'UTR 变体、临床病理参数与化疗反应之间的关系。我们分析了 305 名接受 FAC 方案治疗的乳腺癌女性的 ADME 基因 3'UTR 中的 33 个种系多态性。该研究的临床终点为:总生存期(OS)、无进展生存期(PFS)、无复发生存期(RFS)和总缓解定义为无治疗失败生存期(TFFS)。较短的 OS 与 NR1/2 rs3732359 AA、SLC22A16 rs7756222 CC 以及 SLC22A16 rs9487402 等位基因 G 的存在以及属于 TNM 分类的临床因素有关:肿瘤大小>1cm、淋巴结受累和存在转移。PFS 与两个多态性 PGR rs1824125 GG、PGR rs12224560 CC 和 SLC22A16 rs7756222 CC 以及预先存在的转移有关。由于 DPYD rs291593 CC、AKR1C3 rs3209896 AG 和 PGR 的阴性表达,RFS 缩短。ALDH5A1 rs1054899 等位基因 A 的存在、缺乏化疗前手术以及 PGR 的阴性状态与较差的治疗反应相关。人群中常见的种系变异是决定治疗反应的重要因素。我们观察到遗传和临床因素的积累对不良生存预后和整体治疗反应的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/275f/7109149/f9635b921059/41598_2020_62662_Fig1_HTML.jpg

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