Evidence map›Paper›PMID 36588107›Full record

ReviewSignal transduction and targeted therapy2023

Targeting integrin pathways: mechanisms and advances in therapy.

Xiaocong Pang, Xu He, Zhiwei Qiu, Hanxu Zhang, Ran Xie, Zhiyan Liu, Yanlun Gu, Nan Zhao, Qian Xiang, Yimin Cui

Open access · goldAbstract readReview
In one paragraph

Review in Signal transduction and targeted therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 590 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
590citing papers in PubMed, 1 pooled it
274.0field-weighted citation impact, top 1% 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

590 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,100 citations in OpenAlex.

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  15. Understanding and targeting the tumour matrisome.Nature reviews. Clinical oncology · 2026
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530 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 1 country.

Xiaocong Pang *Department of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China.
Xu He *Department of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China.
Zhiwei Qiu *Department of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China.
Hanxu Zhang *Department of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China.
Ran XieDepartment of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China.
Zhiyan LiuDepartment of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China.
Yanlun GuDepartment of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China.
Nan ZhaoDepartment of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China.
Qian XiangDepartment of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China. xiangqz@126.com.
Yimin CuiDepartment of Pharmacy, Peking University First Hospital, Xishiku Street, Xicheng District, 100034, Beijing, China. cui.pharm@pkufh.com.
Peking University · CNPeking University First Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Integrins are considered the main cell-adhesion transmembrane receptors that play multifaceted roles as extracellular matrix (ECM)-cytoskeletal linkers and transducers in biochemical and mechanical signals between cells and their environment in a wide range of states in health and diseases. Integrin functions are dependable on a delicate balance between active and inactive status via multiple mechanisms, including protein-protein interactions, conformational changes, and trafficking. Due to their exposure on the cell surface and sensitivity to the molecular blockade, integrins have been investigated as pharmacological targets for nearly 40 years, but given the complexity of integrins and sometimes opposite characteristics, targeting integrin therapeutics has been a challenge. To date, only seven drugs targeting integrins have been successfully marketed, including abciximab, eptifibatide, tirofiban, natalizumab, vedolizumab, lifitegrast, and carotegrast. Currently, there are approximately 90 kinds of integrin-based therapeutic drugs or imaging agents in clinical studies, including small molecules, antibodies, synthetic mimic peptides, antibody-drug conjugates (ADCs), chimeric antigen receptor (CAR) T-cell therapy, imaging agents, etc. A serious lesson from past integrin drug discovery and research efforts is that successes rely on both a deep understanding of integrin-regulatory mechanisms and unmet clinical needs. Herein, we provide a systematic and complete review of all integrin family members and integrin-mediated downstream signal transduction to highlight ongoing efforts to develop new therapies/diagnoses from bench to clinic. In addition, we further discuss the trend of drug development, how to improve the success rate of clinical trials targeting integrin therapies, and the key points for clinical research, basic research, and translational research.

Indexed as

Cell CommunicationIntegrinsCell AdhesionPeptidesSignal TransductionIntegrinsPeptides

Identifiers

PMID36588107
PMCPMC9805914
OpenAlexW4313382384

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.