Evidence map›Paper›PMID 32514188›Full record

ReviewExperimental & molecular medicine2020

Targeting focal adhesion kinase in cancer cells and the tumor microenvironment.

James M Murphy, Yelitza A R Rodriguez, Kyuho Jeong, Eun-Young Erin Ahn, Ssang-Taek Steve Lim

Open access · goldAbstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed, 1 pooled it
14.9field-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

130 citing papers in PubMed, 1 synthesis or guideline pooled it, 217 citations in OpenAlex.

  1. Pooled it
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  5. In Vitro Anti-Breast Cancer Effects ofInternational journal of molecular sciences · 2026
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  10. Progenitor CD8Apoptosis : an international journal on programmed cell death · 2026
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70 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

5 authors at 2 institutions in 1 country.

James M Murphy *Department of Biochemistry and Molecular Biology, University of South Alabama, College of Medicine, Mobile, AL, 36688, USA.
Yelitza A R Rodriguez *Department of Biochemistry and Molecular Biology, University of South Alabama, College of Medicine, Mobile, AL, 36688, USA.
Kyuho JeongDepartment of Biochemistry and Molecular Biology, University of South Alabama, College of Medicine, Mobile, AL, 36688, USA.
Eun-Young Erin AhnDepartment of Pathology, O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.ORCID http://orcid.org/0000-0001-8795-7734
Ssang-Taek Steve LimDepartment of Biochemistry and Molecular Biology, University of South Alabama, College of Medicine, Mobile, AL, 36688, USA. stlim@southalabama.edu.ORCID http://orcid.org/0000-0003-0323-8607
University of South Alabama · USUniversity of Alabama at Birmingham · US

Funding

SON-mediated gene expression and leukemiaR01CA190688 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI AHN, ERIN EUN-YOUNG · 2016 to 2021
$1.7M
Role of FAK in vascular inflammationR01HL136432 · NHLBI · UNIVERSITY OF SOUTH ALABAMA · PI LIM, STEVE · 2017 to 2020
$1.6M
NCI NIH HHS R01 CA190688NHLBI NIH HHS R01 HL136432
6 · The paper itself

Abstract

Focal adhesion kinase (FAK) is an integrin-associated protein tyrosine kinase that is frequently overexpressed in advanced human cancers. Recent studies have demonstrated that aside from FAK's catalytic activity in cancer cells, its cellular localization is also critical for regulating the transcription of chemokines that promote a favorable tumor microenvironment (TME) by suppressing destructive host immunity. In addition to the protumor roles of FAK in cancer cells, FAK activity within cells of the TME may also support tumor growth and metastasis through various mechanisms, including increased angiogenesis and vascular permeability and effects related to fibrosis in the stroma. Small molecule FAK inhibitors have demonstrated efficacy in alleviating tumor growth and metastasis, and some are currently in clinical development phases. However, several preclinical trials have shown increased benefits from dual therapies using FAK inhibitors in combination with other chemotherapies or with immune cell activators. This review will discuss the role of nuclear FAK as a driver for tumor cell survival as well as potential therapeutic strategies to target FAK in both tumors and the TME.

Indexed as

AnimalsFocal Adhesion Protein-Tyrosine KinasesHumansTumor MicroenvironmentFocal Adhesion Protein-Tyrosine Kinases

Identifiers

PMID32514188
PMCPMC7338452
OpenAlexW3033435356

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.