Evidence map›Paper›PMID 36713578›Full record

ArticleFrontiers in oncology2022

DNA methylation-based patterns for early diagnostic prediction and prognostic evaluation in colorectal cancer patients with high tumor mutation burden.

Hao Huang, Weifan Cao, Zhiping Long, Lei Kuang, Xi Li, Yifei Feng, Yuying Wu, Yang Zhao, Yinggang Chen, Peng Sun and 11 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.6field-weighted citation impact, top 8% of its field
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

11 citing papers in PubMed, 14 citations in OpenAlex.

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  11. [Molecular pathology of colorectal cancer].Pathologie (Heidelberg, Germany) · 2023
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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 at 5 institutions in 1 country.

Hao HuangDepartment of General Practice, The Affiliated Luohu Hospital of Shenzhen University Health Science Center, Shenzhen, Guangdong, China.
Weifan CaoDepartment of General Practice, The Affiliated Luohu Hospital of Shenzhen University Health Science Center, Shenzhen, Guangdong, China.
Zhiping LongDepartment of Epidemiology, Public Health School of Harbin Medical University, Harbin, China.
Lei KuangDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Xi LiDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Yifei FengDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Yuying WuDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Yang ZhaoDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Yinggang ChenDepartment of Gastrointestinal Surgery, Shenzhen Hospital, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Peng SunDepartment of Gastrointestinal Surgery, Shenzhen Hospital, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Panxin PengDepartment of Gastrointestinal Surgery, Shenzhen Hospital, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Jinli ZhangDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Lijun YuanDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Tianze LiDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Huifang HuDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Gairui LiDepartment of Chronic Disease Control and Prevention, Shenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Longkun YangDepartment of Epidemiology and Health Statistics, Fujian Provincial Key Laboratory of Environment Factors and Cancer, School of Public Health, Fujian Medical University, Fuzhou, China.
Xing ZhangDepartment of Epidemiology and Health Statistics, Fujian Provincial Key Laboratory of Environment Factors and Cancer, School of Public Health, Fujian Medical University, Fuzhou, China.
Fulan HuDepartment of Epidemiology and Health Statistics, School of Public Health, Shenzhen University Health Science Center, Shenzhen, China.
Xizhuo SunDepartment of General Practice, The Affiliated Luohu Hospital of Shenzhen University Health Science Center, Shenzhen, Guangdong, China.
Dongsheng HuDepartment of General Practice, The Affiliated Luohu Hospital of Shenzhen University Health Science Center, Shenzhen, Guangdong, China.
Shenzhen University Health Science Center · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNFujian Medical University · CNHarbin Medical University · CNShenzhen Nanshan Center for Chronic Disease Control · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune checkpoint inhibitor (ICI) therapy has proven to be a promising treatment for colorectal cancer (CRC). We aim to investigate the relationship between DNA methylation and tumor mutation burden (TMB) by integrating genomic and epigenetic profiles to precisely identify clinical benefit populations and to evaluate the effect of ICI therapy. Methods: A total of 536 CRC tissues from the Cancer Genome Atlas (TCGA) with mutation data were collected and subjected to calculate TMB. 80 CRC patients with high TMB and paired normal tissues were selected as training sets and developed the diagnostic and prognostic methylation models, respectively. In the validation set, the diagnostic model was validated in our in-house 47 CRC tissues and 122 CRC tissues from the Gene Expression Omnibus (GEO) datasets, respectively. And a total of 38 CRC tissues with high TMB from the COLONOMICS dataset verified the prognostic model. Results: A positive correlation between differential methylation positions and TMB level was observed in TCGA CRC cohort (r=0.45). The diagnostic score that consisted of methylation levels of four genes ( Conclusions: By integrating analyses of methylation and mutation data, it is suggested that DNA methylation patterns combined with TMB serve as a novel potential biomarker for early screening in more high-TMB populations and for evaluating the prognostic effect of CRC patients with ICI therapy.

Indexed as

colorectal cancerDNA methylationimmunotherapyTCGATMB

Identifiers

PMID36713578
PMCPMC9880489
OpenAlexW4316041480

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.