转录组
癌症
乳腺癌
肺癌
生物
基因
癌症研究
癌细胞
计算生物学
癌症检测
核糖核酸
基因表达
生物标志物
病理
医学
遗传学
作者
Matthew H. Larson,Wenying Pan,Hyunsung John Kim,Ruth E. Mauntz,Sarah Stuart,Monica Pimentel,Yuanyuan Zhou,Per Knudsgaard,Vasiliki Demas,Alex Aravanis,Arash Jamshidi
标识
DOI:10.1038/s41467-021-22444-1
摘要
Abstract Cell-free RNA (cfRNA) is a promising analyte for cancer detection. However, a comprehensive assessment of cfRNA in individuals with and without cancer has not been conducted. We perform the first transcriptome-wide characterization of cfRNA in cancer (stage III breast [ n = 46], lung [ n = 30]) and non-cancer ( n = 89) participants from the Circulating Cell-free Genome Atlas (NCT02889978). Of 57,820 annotated genes, 39,564 (68%) are not detected in cfRNA from non-cancer individuals. Within these low-noise regions, we identify tissue- and cancer-specific genes, defined as “dark channel biomarker” (DCB) genes, that are recurrently detected in individuals with cancer. DCB levels in plasma correlate with tumor shedding rate and RNA expression in matched tissue, suggesting that DCBs with high expression in tumor tissue could enhance cancer detection in patients with low levels of circulating tumor DNA. Overall, cfRNA provides a unique opportunity to detect cancer, predict the tumor tissue of origin, and determine the cancer subtype.
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