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DNA损伤反应基因中的致病变异谱与墨西哥梅斯蒂索人群转移性乳腺癌的无进展生存期相关。

Pathogenic variant profile in DNA damage response genes correlates with metastatic breast cancer progression-free survival in a Mexican-mestizo population.

作者信息

Vázquez-Romo Rafael, Millan-Catalan Oliver, Ruíz-García Erika, Martínez-Gutiérrez Antonio D, Alvarado-Miranda Alberto, Campos-Parra Alma D, López-Camarillo César, Jacobo-Herrera Nadia, López-Urrutia Eduardo, Guardado-Estrada Mariano, Cantú de León David, Pérez-Plasencia Carlos

机构信息

Departamento de Cirugía de Tumores Mamarios, Instituto Nacional de Cancerología (INCan), Ciudad de México, Mexico.

Laboratorio de Genómica, Instituto Nacional de Cancerología (INCan), Ciudad de México, Mexico.

出版信息

Front Oncol. 2023 Apr 27;13:1146008. doi: 10.3389/fonc.2023.1146008. eCollection 2023.

Abstract

INTRODUCTION

Metastatic breast cancer causes the most breast cancer-related deaths around the world, especially in countries where breast cancer is detected late into its development. Genetic testing for cancer susceptibility started with the BRCA 1 and 2 genes. Still, recent research has shown that variations in other members of the DNA damage response (DDR) are also associated with elevated cancer risk, opening new opportunities for enhanced genetic testing strategies.

METHODS

We sequenced BRCA1/2 and twelve other DDR genes from a Mexican-mestizo population of 40 metastatic breast cancer patients through semiconductor sequencing.

RESULTS

Overall, we found 22 variants -9 of them reported for the first time- and a strikingly high proportion of variations in ARID1A. The presence of at least one variant in the ARID1A, BRCA1, BRCA2, or FANCA genes was associated with worse progression-free survival and overall survival in our patient cohort.

DISCUSSION

Our results reflected the unique characteristics of the Mexican-mestizo population as the proportion of variants we found differed from that of other global populations. Based on these findings, we suggest routine screening for variants in ARID1A along with BRCA1/2 in breast cancer patients from the Mexican-mestizo population.

摘要

引言

转移性乳腺癌导致全球范围内与乳腺癌相关的死亡人数最多,尤其是在那些乳腺癌发现较晚的国家。癌症易感性的基因检测始于BRCA 1和2基因。然而,最近的研究表明,DNA损伤反应(DDR)其他成员的变异也与癌症风险升高有关,为增强基因检测策略带来了新机遇。

方法

我们通过半导体测序对来自墨西哥混血人群的40例转移性乳腺癌患者的BRCA1/2和其他12个DDR基因进行了测序。

结果

总体而言,我们发现了22种变异——其中9种是首次报道——并且ARID1A中的变异比例惊人地高。在我们的患者队列中,ARID1A、BRCA1、BRCA2或FANCA基因中至少存在一种变异与无进展生存期和总生存期较差相关。

讨论

我们的结果反映了墨西哥混血人群的独特特征,因为我们发现的变异比例与其他全球人群不同。基于这些发现,我们建议对墨西哥混血人群的乳腺癌患者常规筛查ARID1A以及BRCA1/2中的变异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10174330/ce8ae5830e05/fonc-13-1146008-g001.jpg

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