Evidence map›Paper›PMID 35353239›Full record

ArticleCancer immunology, immunotherapy : CII2022

OIT3 mediates macrophage polarization and facilitates hepatocellular carcinoma progression.

Shuai Yang, Jiangang Zhang, Yanquan Xu, Jingchun Wang, Huakan Zhao, Juan Lei, Yu Zhou, Yu Chen, Lei Wu, Mingyue Zhou and 3 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 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
1.4field-weighted citation impact, top 20% 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, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Profiling Genome-Wide Methylation Patterns in Cattle Infected withInternational journal of molecular sciences · 2024
    Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  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

13 authors at 2 institutions in 1 country.

Shuai Yang *Clinical Medicine Research Center, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.
Jiangang Zhang *Clinical Medicine Research Center, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.
Yanquan XuClinical Medicine Research Center, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.
Jingchun WangClinical Medicine Research Center, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.
Huakan ZhaoDepartment of Medical Oncology, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Juan LeiDepartment of Medical Oncology, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Yu ZhouDepartment of Medical Oncology, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Yu ChenDepartment of Medical Oncology, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Lei WuDepartment of Medical Oncology, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Mingyue ZhouDepartment of Medical Oncology, Chongqing University Cancer Hospital, Chongqing, 400030, China.
Lu ZhengDepartment of Hepatobiliary Surgery, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China. xqyyzl1@163.com.
Xiaohui JiDepartment of Medical Oncology, Chongqing University Cancer Hospital, Chongqing, 400030, China. 15023245186@163.com.
Yongsheng LiClinical Medicine Research Center, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China. lys@cqu.edu.cn.ORCID http://orcid.org/0000-0003-2175-9449
Chongqing University · CNArmy Medical University · CN

Funding

Chongqing Outstanding Youth Science Foundation No. cstc2020jcyj-jqX0030Major International (Regional) Joint Research Program of the National Natural Science Foundation of China No. 81920108027Natural Science Foundation of Chongqing No. cstc2021jcyj-msxm0926
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most common causes of cancer-related mortality; however, effective immunotherapy strategies are limited because of the immunosuppressive tumor microenvironment. Macrophages are essential components of the HCC microenvironment and are related to poor prognosis. Here, we evaluated the attributes of paracancer tissues in tumor immunity and progression using public databases. Based on the abundance of immune cells estimated by CIBERSORT, we performed weighted gene co-expression network analysis and found a specific module associated with M2 macrophages. Through analyzing interaction networks using Cytoscape and public datasets, we identified oncoprotein-induced transcript 3 (OIT3) as a novel marker of M2 macrophages. Overexpression of OIT3 remodeled immune features and reprogrammed the metabolism of M2 macrophages. Moreover, compared with wildtype macrophages, OIT3-overexpressing macrophages further enhanced the migration and invasion of co-cultured cancer cells. Additionally, OIT3-overexpressing macrophages promoted tumorigenesis and cancer development in vivo. Taken together, the findings demonstrate that OIT3 is a novel biomarker of alternatively activated macrophages and facilitates HCC metastasis.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsBiomarkersCell Line, TumorHumansMacrophagesMembrane ProteinsOncogene ProteinsTumor MicroenvironmentBiomarkersMembrane ProteinsOIT3 protein, humanOncogene ProteinsAlternatively activated macrophagesHepatocellular carcinomaMigration and invasionOIT3ParacancerWeighted gene co-expression network analysis

Identifiers

PMID35353239
PMCPMC10992929
OpenAlexW4220917982

What Socratic holds

Textmetadata
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.