Evidence map›Paper›PMID 38336771›Full record

ArticleClinical epigenetics2024

Tissue of origin prediction for cancer of unknown primary using a targeted methylation sequencing panel.

Miaomiao Sun, Bo Xu, Chao Chen, Youjie Zhu, Xiaomo Li, Kuisheng Chen

Abstract read
In one paragraph

Article in Clinical epigenetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Miaomiao Sun *Department of Pathology, Henan Key Laboratory of Tumor Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Bo Xu *Research and Development Division, Oriomics Biotech Inc, Hangzhou, China.
Chao ChenDepartment of Pathology, Henan Key Laboratory of Tumor Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Youjie ZhuResearch and Development Division, Oriomics Biotech Inc, Hangzhou, China.
Xiaomo LiResearch and Development Division, Oriomics Biotech Inc, Hangzhou, China. lixiaomo62@hotmail.com.
Kuisheng ChenDepartment of Pathology, Henan Key Laboratory of Tumor Pathology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. chenksh2002@163.com.

Funding

Henan Young and Middle-aged Talents in Health Science and Technology Innovation YXKC2022015
6 · The paper itself

Abstract

rationaleCancer of unknown primary (CUP) is a group of rare malignancies with poor prognosis and unidentifiable tissue-of-origin. Distinct DNA methylation patterns in different tissues and cancer types enable the identification of the tissue of origin in CUP patients, which could help risk assessment and guide site-directed therapy.

methodsUsing genome-wide DNA methylation profile datasets from The Cancer Genome Atlas (TCGA) and machine learning methods, we developed a 200-CpG methylation feature classifier for CUP tissue of origin prediction (MFCUP). MFCUP was further validated with public-available methylation array data of 2977 specimens and targeted methylation sequencing of 78 Formalin-fixed paraffin-embedded (FFPE) samples from a single center.

resultsMFCUP achieved an accuracy of 97.2% in a validation cohort (n = 5923) representing 25 cancer types. When applied to an Infinium 450 K array dataset (n = 1052) and an Infinium EPIC (850 K) array dataset (n = 1925), MFCUP achieved an overall accuracy of 93.4% and 84.8%, respectively. Based on MFCUP, we established a targeted bisulfite sequencing panel and validated it with FFPE sections from 78 patients of 20 cancer types. This methylation sequencing panel correctly identified tissue of origin in 88.5% (69/78) of samples. We also found that the methylation levels of specific CpGs can distinguish one cancer type from others, indicating their potential as biomarkers for cancer diagnosis and screening.

conclusionOur methylation-based cancer classifier and targeted methylation sequencing panel can predict tissue of origin in diverse cancer types with high accuracy.

Indexed as

DNA MethylationNeoplasms, Unknown PrimaryHumansSequence Analysis, DNACancer of unknown primaryElastic netMachine learningMethylation classifierRandom forestTargeted methylation sequencingTissue of origin

Identifiers

PMID38336771
PMCPMC10854167

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.