Evidence map›Paper›PMID 40748480›Full record

ReviewHistochemistry and cell biology2025

The ILK-PINCH-parvin complex: a conserved primary adhesome regulating biological processes.

Ushashi Ain, Benazir Fatma, Hena Firdaus

Abstract readReview
PubMed Publisher
In one paragraph

Review in Histochemistry and cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

3 authors.

Ushashi Ain *Department of Life Sciences, Central University of Jharkhand, Cheri-Manatu Campus, Ranchi, 835222, India.
Benazir Fatma *Department of Life Sciences, Central University of Jharkhand, Cheri-Manatu Campus, Ranchi, 835222, India.
Hena FirdausDepartment of Life Sciences, Central University of Jharkhand, Cheri-Manatu Campus, Ranchi, 835222, India. hena.firdaus@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intracellularly expressed integrin associated proteins (IAPs) play pivotal role in facilitating cellular adhesion and survival. The integrin linked kinase (ILK)-PINCH-parvin (IPP) complex regulates cell-matrix interactions crucial for tissue development and homeostasis by functioning as an adapter between integrin and actin cytoskeleton. This review provides a compiled structural and functional insight into the IPP complex and its interacting partners, highlighting its conservation and signalling pathway, addressing a cross-talk across its homologues. Finally, the study sheds light on the association of the complex members with biological processes and disease progression, thus potentiating further exploration of the IPP complex within the integrin signalling pathway.

Indexed as

Microfilament ProteinsProtein Serine-Threonine KinasesAnimalsCalponinsHumansScaffold Protein ILKCalponinsMicrofilament ProteinsPARVA protein, humanProtein Serine-Threonine KinasesScaffold Protein ILKILKIntegrin signallingParvinPINCHRSU1

Identifiers

PMID40748480

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.