Evidence map›Paper›PMID 31934272›Full record

ReviewAmerican journal of translational research2019

ITGB3/CD61: a hub modulator and target in the tumor microenvironment.

Chen Zhu, Ziqing Kong, Biao Wang, Wen Cheng, Anhua Wu, Xin Meng

Open access · greenAbstract readReview
In one paragraph

Review in American journal of translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
2.8field-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

59 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Prognostic model construction and drug prediction in colorectal cancer using mitochondrial programmed cell death-related genes.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  3. Primary Metabolites in ThreeLife (Basel, Switzerland) · 2026
    Article
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  12. Endometriosis: An Immunologist's Perspective.International journal of molecular sciences · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Investigation ofBiology · 2024
    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

6 authors at 2 institutions in 1 country.

Chen ZhuDepartment of Neurosurgery, The First Hospital of China Medical University Shenyang, Liaoning, China.
Ziqing KongDepartment of Biochemistry and Molecular Biology, School of Life Sciences, China Medical University Shenyang, Liaoning, China.
Biao WangDepartment of Biochemistry and Molecular Biology, School of Life Sciences, China Medical University Shenyang, Liaoning, China.
Wen ChengDepartment of Neurosurgery, The First Hospital of China Medical University Shenyang, Liaoning, China.
Anhua WuDepartment of Neurosurgery, The First Hospital of China Medical University Shenyang, Liaoning, China.
Xin MengDepartment of Biochemistry and Molecular Biology, School of Life Sciences, China Medical University Shenyang, Liaoning, China.
First Hospital of China Medical University · CNLiaoning University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

β3 integrin (ITGB3), also known as CD61 or GP3A, is one of the most widely studied components in the integrin family. As an adhesion receptor on the cell surface, ITGB3 participates in reprogramming tumor metabolism, shaping the stromal and immune microenvironment, facilitating epithelial to mesenchymal transition (EMT) and endothelial to mesenchymal transition (End-MT) and maintaining tumor stemness, etc. Recent studies proposed various intervention strategies against ITGB3 and have achieved promising outcomes in several types of tumor. Here, we review the adaption response and cellular crosstalk in the tumor microenvironment mediated by ITGB3, as well as its upstream and downstream signaling pathways. Lastly, we focus on the inhibitors of ITGB3, ultimately indicating that ITGB3 is a promising target in the tumor microenvironment.

Indexed as

immuneITGB3metabolismstemnesstumor microenvironment

Identifiers

PMID31934272
PMCPMC6943458
OpenAlexW3005668035

What OpenQuestion 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 OpenQuestion graph.