Evidence map›Paper›PMID 35574330›Full record

ArticleFrontiers in oncology2022

FAK PROTAC Inhibits Ovarian Tumor Growth and Metastasis by Disrupting Kinase Dependent and Independent Pathways.

Xueyun Huo, Wenjing Zhang, Guannan Zhao, Zhenwen Chen, Peixin Dong, Hidemichi Watari, Ramesh Narayanan, Todd D Tillmanns, Lawrence M Pfeffer, Junming Yue

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  9. PROTACs in Ovarian Cancer: Current Advancements and Future Perspectives.International journal of molecular sciences · 2024
    Review
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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 5 institutions in 3 countries.

Xueyun HuoSchool of Basic Medical Sciences, Capital Medical University, Beijing, China.
Wenjing ZhangDepartment of Genetics, Genomics & Informatics, College of Medicine, University of Tennessee Health Science Center, Memphis, TN, United States.
Guannan ZhaoDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Tennessee Health Science Center, Memphis, TN, United States.
Zhenwen ChenSchool of Basic Medical Sciences, Capital Medical University, Beijing, China.
Peixin DongDepartment of Gynecology, Hokkaido University School of Medicine, Hokkaido University, Sapporo, Japan.
Hidemichi WatariDepartment of Gynecology, Hokkaido University School of Medicine, Hokkaido University, Sapporo, Japan.
Ramesh NarayananCenter for Cancer Research, College of Medicine, University of Tennessee Health Science Center, Memphis, TN, United States.
Todd D TillmannsDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Tennessee Health Science Center, West Cancer Center, Germantown, TN, United States.
Lawrence M PfefferDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Tennessee Health Science Center, Memphis, TN, United States.
Junming YueDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Tennessee Health Science Center, Memphis, TN, United States.
Center for Cancer Research · USHokkaido University · JPUniversity of Tennessee Health Science Center · USCapital Medical University · CNWest Cancer Center · US

Funding

Racial Disparity in the Expression of Androgen Receptor Splice Variants (AR-SVs) in Prostate CancerR01CA229164 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI Ramesh Narayanan · 2019 to 2026
$3.2M
NCI NIH HHS R01 CA229164
6 · The paper itself

Abstract

Focal adhesion kinase (FAK) is highly expressed in a variety of human cancers and is a target for cancer therapy. Since FAK kinase inhibitors only block the kinase activity of FAK, they are not highly effective in clinical trials. FAK also functions as a scaffold protein in a kinase-independent pathway. To effectively target FAK, it is required to block both FAK kinase-dependent and FAK-independent pathways. Thus, we tested a new generation drug FAK PROTAC for ovarian cancer therapy, which blocks both kinase and scaffold activity. We tested the efficacy of FAK PROTAC and its parent kinase inhibitor (VS-6063) in ovarian cancer cell lines

Indexed as

ASAP1FAK PROTACfocal adhesion kinase (FAK)metastasisovarian cancer

Identifiers

PMID35574330
PMCPMC9095959
OpenAlexW4224982817

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.