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中国女性乳腺癌的遗传特征及循环肿瘤 DNA 突变追踪

Genetic landscape of breast cancer and mutation tracking with circulating tumor DNA in Chinese women.

机构信息

Department of Breast Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, P.R. China.

Omigen, Inc., Hangzhou 310000, P.R. China.

出版信息

Aging (Albany NY). 2021 Apr 23;13(8):11860-11876. doi: 10.18632/aging.202888.

Abstract

Considerable efforts have been devoted to exploring the breast cancer mutational landscape to understand its genetic complexity. However, no studies have yet comprehensively elucidated the molecular characterization of breast tumors in Chinese women. This study aimed to determine the potential clinical utility of peripheral blood assessment for circulating tumor-derived DNA (ctDNA) and comprehensively characterize the female Chinese population's genetic mutational spectrum. We used Omi-Seq to create cancer profiles of 273 patients enrolled at The First Affiliated Hospital of Wenzhou Medical University. The gene landscape results indicate and as the most frequently detected genes, followed by in Chinese breast cancer patients. The accuracy of copy number variations in tissue/formalin-fixed and paraffin-embedded samples was 95% with 86% sensitivity and 99% specificity. Moreover, mutation numbers varied between different molecular cell-free DNA subtypes, with the basal-like patients harboring a higher number of variants than the luminal patients. Furthermore, ratio changes in the max ctDNA allele fraction highly correlated with clinical response measurements, including cancer relapse and metastasis. Our data demonstrate that ctDNA characterization using the Omi-Seq platform can extend the capacity of personalized clinical cancer management.

摘要

为了深入了解乳腺癌的遗传复杂性,研究人员投入了大量精力来探索乳腺癌的基因突变图谱。然而,目前还没有研究全面阐明中国女性乳腺癌肿瘤的分子特征。本研究旨在确定外周血循环肿瘤衍生 DNA(ctDNA)评估的潜在临床应用价值,并全面描述中国女性人群的遗传突变谱。我们使用 Omi-Seq 对温州医科大学第一附属医院 273 名患者进行了癌症分析。基因图谱结果显示, 和 是中国乳腺癌患者中最常检测到的基因,其次是 。组织/福尔马林固定和石蜡包埋样本中 拷贝数变异的准确率为 95%,灵敏度为 86%,特异性为 99%。此外,不同分子游离 DNA 亚型之间的突变数量存在差异,基底样患者的变异数量高于腔面型患者。此外,最大 ctDNA 等位基因分数的比值变化与临床反应测量高度相关,包括癌症复发和转移。我们的数据表明,使用 Omi-Seq 平台进行 ctDNA 特征分析可以扩展个性化临床癌症管理的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/8109076/0a83768dd154/aging-13-202888-g001.jpg

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