Evidence map›Paper›PMID 24389213›Full record

ReviewFrontiers in bioscience (Landmark edition)2014

Targeting FAK in human cancer: from finding to first clinical trials.

Vita M Golubovskaya

Open access · bronzeAbstract readReview
In one paragraph

Review in Frontiers in bioscience (Landmark edition), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
10.9field-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

102 citing papers in PubMed, 201 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Focal Adhesion Kinase Variants May Contribute to Risk of Human Myelomeningocele.medRxiv : the preprint server for health sciences · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Assessment of theFrontiers in chemistry · 2024
    Article
  14. Review
  15. Review
  16. FAK/IL-8 axis promotes the proliferation and migration of gastric cancer cells.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2023
    Article
  17. Article
  18. Review
  19. Review
  20. International journal of molecular sciences · 2023
    Article

42 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

1 author at 1 institution in 1 country.

Vita M GolubovskayaDepartment of Surgical Oncology, Roswell Park Cancer Institute, Buffalo, NY.
Roswell Park Comprehensive Cancer Center · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
FOCAL ADHESION KINASE--TUMOR BIOLOGY AND THERAPEUTICSR01CA065910 · NCI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI MARLOWE, TIMOTHY A · 1996 to 2019
$6.3M
Focal Adhesion Kinase - Tumor Biology and TherapeuticsR37CA065910 · NCI · UNIVERSITY OF ARIZONA · PI Timothy A Marlowe · 2022 to 2026
$1.6M
NCI NIH HHS CA 16056NCI NIH HHS P30 CA016056NCI NIH HHS R01 CA065910NCI NIH HHS R01 CA65910NCI NIH HHS R37 CA065910
6 · The paper itself

Abstract

It is twenty years since Focal Adhesion Kinase (FAK) was found to be overexpressed in many types of human cancer. FAK plays an important role in adhesion, spreading, motility, invasion, metastasis, survival, angiogenesis, and recently has been found to play an important role as well in epithelial to mesenchymal transition (EMT), cancer stem cells and tumor microenvironment. FAK has kinase-dependent and kinase independent scaffolding, cytoplasmic and nuclear functions. Several years ago FAK was proposed as a potential therapeutic target; the first clinical trials were just reported, and they supported further studies of FAK as a promising therapeutic target. This review discusses the main functions of FAK in cancer, and specifically focuses on recent novel findings on the role of FAK in cancer stem cells, microenvironment, epithelial-to-mesenchymal transition, invasion, metastasis, and also highlight new approaches of targeting FAK and critically discuss challenges that lie ahead for its targeted therapeutics. The review provides a summary of translational approaches of FAK-targeted and combination therapies and outline perspectives and future directions of FAK research.

Indexed as

Enzyme InhibitorsFocal Adhesion Protein-Tyrosine KinasesHumansNeoplasmsNeoplastic Stem CellsProtein ConformationEnzyme InhibitorsFocal Adhesion Protein-Tyrosine Kinases

Identifiers

PMID24389213
PMCPMC3952878
OpenAlexW2043686550

What Socratic holds

Textmetadata
LicenceTDM
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.