多发性骨髓瘤
生物
DNA测序
病理
计算生物学
基因组
基因
医学
遗传学
免疫学
作者
Ankit K. Dutta,Jean-Baptiste Alberge,Elizabeth D. Lightbody,Cody J. Boehner,Andrew Dunford,Romanos Sklavenitis‐Pistofidis,Tarek H. Mouhieddine,Annie Cowan,Nang Kham Su,Erica Horowitz,Hadley Barr,Laura Hevenor,Jenna B. Beckwith,Jacqueline Perry,Amanda Cao,Ziao Lin,Frank K. Kuhr,Richard G. Del Mastro,Omar Nadeem,Patricia T. Greipp
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2022-12-07
卷期号:13 (2): 348-363
被引量:34
标识
DOI:10.1158/2159-8290.cd-22-0482
摘要
In this study, we established an approach enabling the enumeration and sequencing of CTCs to replace standard molecular cytogenetics. CTCs harbored the same pathognomonic MM abnormalities as BM plasma cells. Longitudinal sampling of serial CTCs was able to track clonal dynamics over time and detect the emergence of high-risk genetic subclones. This article is highlighted in the In This Issue feature, p. 247.
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