Evidence map›Paper›PMID 38970366›Full record

ArticleGenomics, proteomics & bioinformatics2024

Pan-cancer Analysis Reveals m6A Variation and Cell-specific Regulatory Network in Different Cancer Types.

Yao Lin, Jingyi Li, Shuaiyi Liang, Yaxin Chen, Yueqi Li, Yixian Cun, Lei Tian, Yuanli Zhou, Yitong Chen, Jiemei Chu and 7 more

Abstract read
In one paragraph

Article in Genomics, proteomics & bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. cGAMP suppresses FTO expression to promote mCellular and molecular life sciences : CMLS · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Research Status and Latest Progress in the Regulatory Mechanisms of ABCA1.International journal of molecular sciences · 2025
    Review
  10. CAPRIN1 specifically mediates mCommunications biology · 2025
    Article
  11. Article
  12. Pan-cancer analysis ofGenes & diseases · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Journal of inflammation research · 2025
    Article
  19. Article
  20. Article
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

17 authors.

Yao LinLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0000-0003-1728-3791
Jingyi LiLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0009-0002-6440-5106
Shuaiyi LiangDepartment of Bioinformatics, Anjin Biotechnology Co., Ltd., Guangzhou 510000, China.ORCID 0000-0001-8099-6159
Yaxin ChenFrontiers Science Center for Disease-related Molecular Network, Precision Medicine Research Center, West China Hospital, Department of Respiratory and Critical Care Medicine, Sichuan University, Chengdu 610041, China.ORCID 0000-0002-5469-7080
Yueqi LiSchool of Basic Medical Sciences, Guangxi Medical University, Nanning 530021, China.ORCID 0000-0002-2640-4906
Yixian CunDepartment of Medical Bioinformatics, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.ORCID 0000-0002-3951-942X
Lei TianThe First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.ORCID 0000-0002-5268-5270
Yuanli ZhouThe First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.ORCID 0000-0001-8855-489X
Yitong ChenThe First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.ORCID 0000-0002-2577-2897
Jiemei ChuLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0000-0003-2942-0490
Hubin ChenLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0009-0003-0216-7138
Qiang LuoLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0000-0002-3753-7325
Ruili ZhengLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0000-0002-3246-0269
Gang WangLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0000-0001-7264-2457
Hao LiangLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0000-0001-7534-5124
Ping CuiLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0000-0001-7195-2832
Sanqi AnLife Sciences Institute, Biosafety Level-3 Laboratory, Guangxi Medical University, Nanning 530021, China.ORCID 0000-0002-3177-213X

Funding

Guangxi Science and Technology Base and Talent Project 2022AC19006National Natural Science Foundation of China 82160389
6 · The paper itself

Abstract

As the most abundant messenger RNA (mRNA) modification, N6-methyladenosine (m6A) plays a crucial role in RNA fate, impacting cellular and physiological processes in various tumor types. However, our understanding of the role of the m6A methylome in tumor heterogeneity remains limited. Herein, we collected and analyzed m6A methylomes across nine human tissues from 97 m6A sequencing (m6A-seq) and RNA sequencing (RNA-seq) samples. Our findings demonstrate that m6A exhibits different heterogeneity in most tumor tissues compared to normal tissues, which contributes to the diverse clinical outcomes in different cancer types. We also found that the cancer type-specific m6A level regulated the expression of different cancer-related genes in distinct cancer types. Utilizing a novel and reliable method called "m6A-express", we predicted m6A-regulated genes and revealed that cancer type-specific m6A-regulated genes contributed to the prognosis, tumor origin, and infiltration level of immune cells in diverse patient populations. Furthermore, we identified cell-specific m6A regulators that regulate cancer-specific m6A and constructed a regulatory network. Experimental validation was performed, confirming that the cell-specific m6A regulator CAPRIN1 controls the m6A level of TP53. Overall, our work reveals the clinical relevance of m6A in various tumor tissues and explains how such heterogeneity is established. These results further suggest the potential of m6A in cancer precision medicine for patients with different cancer types.

Indexed as

AdenosineGene Regulatory NetworksNeoplasmsGene Expression Regulation, NeoplasticHumansRNA, MessengerAdenosineN-methyladenosineRNA, MessengerCell-specificHeterogeneitym6A-regulated genem6A regulatorN 6-methyladenosine

Identifiers

PMID38970366
PMCPMC11514823

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.