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Tumor fractions deciphered from circulating cell-free DNA methylation for cancer early diagnosis.


ABSTRACT: Tumor-derived circulating cell-free DNA (cfDNA) provides critical clues for cancer early diagnosis, yet it often suffers from low sensitivity. Here, we present a cancer early diagnosis approach using tumor fractions deciphered from circulating cfDNA methylation signatures. We show that the estimated fractions of tumor-derived cfDNA from cancer patients increase significantly as cancer progresses in two independent datasets. Employing the predicted tumor fractions, we establish a Bayesian diagnostic model in which training samples are only derived from late-stage patients and healthy individuals. When validated on early-stage patients and healthy individuals, this model exhibits a sensitivity of 86.1% for cancer early detection and an average accuracy of 76.9% for tumor localization at a specificity of 94.7%. By highlighting the potential of tumor fractions on cancer early diagnosis, our approach can be further applied to cancer screening and tumor progression monitoring.

SUBMITTER: Zhou X 

PROVIDER: S-EPMC9744803 | biostudies-literature | 2022 Dec

REPOSITORIES: biostudies-literature

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Tumor fractions deciphered from circulating cell-free DNA methylation for cancer early diagnosis.

Zhou Xiao X   Cheng Zhen Z   Dong Mingyu M   Liu Qi Q   Yang Weiyang W   Liu Min M   Tian Junzhang J   Cheng Weibin W  

Nature communications 20221213 1


Tumor-derived circulating cell-free DNA (cfDNA) provides critical clues for cancer early diagnosis, yet it often suffers from low sensitivity. Here, we present a cancer early diagnosis approach using tumor fractions deciphered from circulating cfDNA methylation signatures. We show that the estimated fractions of tumor-derived cfDNA from cancer patients increase significantly as cancer progresses in two independent datasets. Employing the predicted tumor fractions, we establish a Bayesian diagnos  ...[more]

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