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HR+/HER2-转移性乳腺癌内分泌耐药的分子特征分析:液体活检中细胞外囊泡衍生DNA和循环肿瘤DNA的见解

Molecular Profiling of Endocrine Resistance in HR+/HER2-Metastatic Breast Cancer: Insights from Extracellular Vesicles-Derived DNA and ctDNA in Liquid Biopsies.

作者信息

Martínez-Rodríguez Ana, Fuentes-Antrás Jesús, Lorca Víctor, López de Sá Alfonso, Pérez-Segura Pedro, Moreno Fernando, García-Sáenz Jose Angel, García-Barberán Vanesa

机构信息

"Clinical and Translational Research in Oncology" Group, Molecular Oncology Laboratory, Hospital Clinico San Carlos, Instituto de Investigación Sanitaria Hospital Clinico San Carlos (IdISSC), 28040 Madrid, Spain.

Department of Medical Oncology, Hospital Clinico San Carlos, Instituto de Investigación Sanitaria Hospital Clinico San Carlos (IdISSC), 28040 Madrid, Spain.

出版信息

Int J Mol Sci. 2024 Dec 4;25(23):13045. doi: 10.3390/ijms252313045.

DOI:10.3390/ijms252313045
PMID:39684756
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11641624/
Abstract

Standard treatments in hormone receptor-positive (HR+)/HER2-metastatic breast cancer (mBC) typically involve endocrine therapy (ET) combined with CDK4/6 inhibitors, yet resistance to ET remains a persistent challenge in advanced cases. A deeper knowledge of the use of liquid biopsy is crucial for the implementation of precision medicine in mBC with real-time treatment guidance. Our study assesses the prognostic value of and mutations in DNA derived from extracellular vesicles (EV-DNA) in longitudinal plasma from 59 HR+/HER2-mBC patients previously exposed to aromatase inhibitors, with a comparative analysis against circulating tumor DNA (ctDNA). Mutations were evaluated by digital PCR. and mutations were found in 22 and 25% of patients. Baseline mutations in EV-DNA were associated with shorter progression-free survival (PFS) across the cohort, with the Y537S mutation showing a particularly strong impact on the outcome of fulvestrant-treated patients. In contrast, mutations in EV-DNA did not significantly correlate with PFS, whereas in ctDNA, they were linked to poor outcomes. Altogether, this study positions EV-DNA as a valuable biomarker alongside ctDNA, enriching the understanding of different analytes in liquid biopsy and supporting strategies for HR+/HER2-mBC in precision oncology.

摘要

激素受体阳性(HR+)/人表皮生长因子受体2阴性转移性乳腺癌(mBC)的标准治疗通常包括内分泌治疗(ET)联合细胞周期蛋白依赖性激酶4/6抑制剂,但在晚期病例中,对ET的耐药性仍然是一个持续存在的挑战。深入了解液体活检的应用对于在mBC中实施精准医学并提供实时治疗指导至关重要。我们的研究评估了59例先前接受过芳香化酶抑制剂治疗的HR+/HER2-mBC患者纵向血浆中源自细胞外囊泡的DNA(EV-DNA)中 和 突变的预后价值,并与循环肿瘤DNA(ctDNA)进行了对比分析。通过数字PCR评估突变情况。在22%和25%的患者中发现了 和 突变。队列中,EV-DNA的基线 突变与无进展生存期(PFS)缩短相关,Y537S突变对氟维司群治疗患者的结局影响尤为显著。相比之下,EV-DNA中的 突变与PFS无显著相关性,而在ctDNA中,它们与不良结局相关。总之,本研究将EV-DNA定位为与ctDNA一样有价值的生物标志物,丰富了对液体活检中不同分析物的理解,并支持了HR+/HER2-mBC在精准肿瘤学中的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5db/11641624/4538eeab325f/ijms-25-13045-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5db/11641624/8c26271ad27c/ijms-25-13045-g003.jpg
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