Evidence map›Paper›PMID 35816095›Full record

ArticleeLife2022

Cancer type classification using plasma cell-free RNAs derived from human and microbes.

Shanwen Chen, Yunfan Jin, Siqi Wang, Shaozhen Xing, Yingchao Wu, Yuhuan Tao, Yongchen Ma, Shuai Zuo, Xiaofan Liu, Yichen Hu and 11 more

Abstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Shanwen Chen *Division of General Surgery, Peking University First Hospital, Beijing, China.
Yunfan Jin *MOE Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua University, Beijing, China.
Siqi Wang *MOE Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua University, Beijing, China.
Shaozhen Xing *MOE Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua University, Beijing, China.
Yingchao WuDivision of General Surgery, Peking University First Hospital, Beijing, China.
Yuhuan TaoMOE Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua University, Beijing, China.
Yongchen MaDivision of General Surgery, Peking University First Hospital, Beijing, China.
Shuai ZuoDivision of General Surgery, Peking University First Hospital, Beijing, China.
Xiaofan LiuMOE Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua University, Beijing, China.
Yichen HuState Key Laboratory of Food Science and Technology, Nanchang University, Nanchang, China.
Hongyan ChenState Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yuandeng LuoInstitute of Hepatobiliary Surgery, The First Hospital Affiliated to Army Medical University, Chongqing, China.
Feng XiaInstitute of Hepatobiliary Surgery, The First Hospital Affiliated to Army Medical University, Chongqing, China.
Chuanming XieInstitute of Hepatobiliary Surgery, The First Hospital Affiliated to Army Medical University, Chongqing, China.
Jianhua YinDepartment of Epidemiology, Faculty of Navy Medicine, Navy Medical University, Shanghai, China.
Xin WangDepartment of Breast Surgical Oncology, National Cancer Center/National Clinical Research Center for Cancer /Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Zhihua LiuState Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Ning ZhangTranslational Cancer Research Center, Peking University First Hospital, Beijing, China.
Zhenjiang Zech XuState Key Laboratory of Food Science and Technology, Nanchang University, Nanchang, China.ORCID 0000-0003-1080-024X
Zhi John LuMOE Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua University, Beijing, China.
Pengyuan WangDivision of General Surgery, Peking University First Hospital, Beijing, China.ORCID 0000-0002-1210-4056

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The utility of cell-free nucleic acids in monitoring cancer has been recognized by both scientists and clinicians. In addition to human transcripts, a fraction of cell-free nucleic acids in human plasma were proven to be derived from microbes and reported to have relevance to cancer. To obtain a better understanding of plasma cell-free RNAs (cfRNAs) in cancer patients, we profiled cfRNAs in ~300 plasma samples of 5 cancer types (colorectal cancer, stomach cancer, liver cancer, lung cancer, and esophageal cancer) and healthy donors (HDs) with RNA-seq. Microbe-derived cfRNAs were consistently detected by different computational methods when potential contaminations were carefully filtered. Clinically relevant signals were identified from human and microbial reads, and enriched Kyoto Encyclopedia of Genes and Genomes pathways of downregulated human genes and higher prevalence torque teno viruses both suggest that a fraction of cancer patients were immunosuppressed. Our data support the diagnostic value of human and microbe-derived plasma cfRNAs for cancer detection, as an area under the ROC curve of approximately 0.9 for distinguishing cancer patients from HDs was achieved. Moreover, human and microbial cfRNAs both have cancer type specificity, and combining two types of features could distinguish tumors of five different primary locations with an average recall of 60.4%. Compared to using human features alone, adding microbial features improved the average recall by approximately 8%. In summary, this work provides evidence for the clinical relevance of human and microbe-derived plasma cfRNAs and their potential utilities in cancer detection as well as the determination of tumor sites.

Indexed as

Cell-Free Nucleic AcidsLung NeoplasmsBiomarkers, TumorHumansPlasmaRNA-SeqROC CurveBiomarkers, TumorCell-Free Nucleic Acidsbiomarkercancer classificationcell-free RNAcomputational biologygeneticsgenomicshumanliquid biopsymicrobiomesystems biology

Identifiers

PMID35816095
PMCPMC9273212

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.