Evidence map›Paper›PMID 35497876›Full record

ArticleJournal of immunology research2022

Histone Methyltransferase SETDB1 Promotes Immune Evasion in Colorectal Cancer

Jiale Tian, Weiwei Wang, Jichao Zhu, Yun Zhuang, Chunrun Qi, Zhengxin Cai, Wenhui Yan, Wenying Lu, Anquan Shang

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
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  7. The Roles of H3K9me3 Writers, Readers, and Erasers in Cancer Immunotherapy.International journal of molecular sciences · 2024
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. miR-22 gene therapy treats HCC by promoting anti-tumor immunity and enhancing metabolism.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  14. Review
  15. Review
  16. Review
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

9 authors at 4 institutions in 1 country.

Jiale TianDepartment of Laboratory Medicine, Shanghai Tongji Hospital, School of Medicine, Tongji University, Shanghai 200065, China.ORCID https://orcid.org/0000-0001-6547-9655
Weiwei WangDepartment of Pathology, Tinghu People's Hospital of Yancheng City, Yancheng 224005, China.ORCID https://orcid.org/0000-0002-3366-7886
Jichao ZhuDepartment of Laboratory Medicine, Huzhou Central Hospital, Affiliated Central Hospital of Huzhou Normal University, Huzhou 313003, China.ORCID https://orcid.org/0000-0003-1727-2267
Yun ZhuangDepartment of Immunology, School of Biology and Basic Medical Sciences, Medical College, Soochow University, Suzhou 215123, China.ORCID https://orcid.org/0000-0001-8805-6858
Chunrun QiDepartment of Pathology, Tinghu People's Hospital of Yancheng City, Yancheng 224005, China.ORCID https://orcid.org/0000-0002-6282-2718
Zhengxin CaiDepartment of Laboratory Medicine, Tinghu People's Hospital of Yancheng City, Yancheng 224005, China.ORCID https://orcid.org/0000-0001-9782-5436
Wenhui YanDepartment of Laboratory Medicine, Tinghu People's Hospital of Yancheng City, Yancheng 224005, China.ORCID https://orcid.org/0000-0002-2508-5616
Wenying LuDepartment of Pathology, Tinghu People's Hospital of Yancheng City, Yancheng 224005, China.ORCID https://orcid.org/0000-0002-3246-9108
Anquan ShangDepartment of Laboratory Medicine, Shanghai Tongji Hospital, School of Medicine, Tongji University, Shanghai 200065, China.ORCID https://orcid.org/0000-0003-2820-1982
Nantong University · CNYancheng Third People's Hospital · CNTongji University · CNHuzhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumors may develop a variety of immune evasion mechanisms during the progression of colorectal cancer (CRC). Here, we intended to explore the mechanism of histone methyltransferase SETDB1 in immune evasion in CRC. The expression of SETDB1, microRNA-22 (miR-22), BATF3, PD-L1, and FOSB in CRC tissues and cells was determined with their interactions analyzed also. Gain-of-function and loss-of-function approaches were employed to evaluate the effects of the SETDB1/FOSB/miR-22/BATF3/PD-L1 axis on T cell function, immune cell infiltration, and tumorigenesis. Aberrant high SETDB1 expression in CRC was positively associated with PD-L1 expression. SETDB1 negatively regulated miR-22 expression by downregulating FOSB expression, while miR-22 downregulated PD-L1 expression

Indexed as

Colorectal NeoplasmsMicroRNAsAnimalsB7-H1 AntigenBasic-Leucine Zipper Transcription FactorsDown-RegulationHistone-Lysine N-MethyltransferaseHistone MethyltransferasesImmune EvasionMiceProto-Oncogene Proteins c-fosRepressor ProteinsB7-H1 AntigenBasic-Leucine Zipper Transcription FactorsFosb protein, mouseHistone-Lysine N-MethyltransferaseHistone MethyltransferasesMicroRNAsProto-Oncogene Proteins c-fosRepressor ProteinsSETDB1 protein, mouse

Identifiers

PMID35497876
PMCPMC9045983
OpenAlexW4224222705

What Socratic 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 Socratic graph.