Evidence map›Paper›PMID 28753606›Full record

ArticlePLoS genetics2017

The RhoJ-BAD signaling network: An Achilles' heel for BRAF mutant melanomas.

Rolando Ruiz, Sohail Jahid, Melissa Harris, Diego M Marzese, Francisco Espitia, Priya Vasudeva, Chi-Fen Chen, Sebastien de Feraudy, Jie Wu, Daniel L Gillen and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Elucidating the Associated Biological Function and Clinical Significance ofInternational journal of molecular sciences · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Rho GTPases in Retinal Vascular Diseases.International journal of molecular sciences · 2021
    Review
  14. Rhoj Is a Novel Target for Progression and Invasion of Glioblastoma by Impairing Cytoskeleton Dynamics.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Article
  15. Article
  16. Targeting Rho GTPase Signaling Networks in Cancer.Frontiers in cell and developmental biology · 2020
    Review
  17. Article
  18. Discovery of a small-molecule inhibitor of specific serine residue BAD phosphorylation.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  19. 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

15 authors at 4 institutions in 1 country.

Rolando RuizDepartment of Biological Chemistry, University of California, Irvine, Irvine, CA, United States of America.
Sohail JahidDepartment of Dermatology, University of California, Irvine, Irvine, CA, United States of America.
Melissa HarrisDepartment of Biology, The University of Alabama at Birmingham, Birmingham, AL, United States of America.
Diego M MarzeseDepartment of Translational Molecular Medicine, Division Molecular Oncology, John Wayne Cancer Institute (JWCI), Providence Saint John's Health Center, Santa Monica, CA, United States of America.ORCID http://orcid.org/0000-0002-3258-8852
Francisco EspitiaDepartment of Dermatology, University of California, Irvine, Irvine, CA, United States of America.
Priya VasudevaDepartment of Dermatology, University of California, Irvine, Irvine, CA, United States of America.
Chi-Fen ChenDepartment of Dermatology, University of California, Irvine, Irvine, CA, United States of America.
Sebastien de FeraudyDepartment of Dermatology, University of California, Irvine, Irvine, CA, United States of America.
Jie WuDepartment of Biological Chemistry, University of California, Irvine, Irvine, CA, United States of America.
Daniel L GillenDepartment of Statistics, University of California, Irvine, Irvine, CA, United States of America.
Tatiana B KrasievaLaser Microbeam and Medical Program, Beckman Laser Institute, University of California, Irvine, Irvine, CA, United States of America.
Bruce J TrombergLaser Microbeam and Medical Program, Beckman Laser Institute, University of California, Irvine, Irvine, CA, United States of America.
William J PavanNational Human Genome Research Institute, National Institute of Health, Bethesda, MD, United States of America.
Dave S HoonDepartment of Translational Molecular Medicine, Division Molecular Oncology, John Wayne Cancer Institute (JWCI), Providence Saint John's Health Center, Santa Monica, CA, United States of America.
Anand K GanesanDepartment of Biological Chemistry, University of California, Irvine, Irvine, CA, United States of America.
University of California, Irvine · USSaint John's Health Center · USNational Human Genome Research Institute · USUniversity of Alabama at Birmingham · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI John Lowengrub · 1994 to 2026
$57.9M
University of California Health Participation in the National COVID Cohort Collaborative (N3C)UL1TR001414 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M, VILAIN, ERIC J. · 2015 to 2023
$35.1M
ANALYSIS OF DOMINANT MEGACOLON--ANOTHER MODEL FORHIRSCHSPRUNG DISEASEZIAHG000070 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI PAVAN, WILLIAM J · 2009 to 2023
$13.4M
Institutional Career Development CoreKL2TR001416 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CAIOZZO, VINCENT JAMES, DEMETRIOU, MICHAEL · 2015 to 2023
$5.6M
Identification of Melanoma Brain Metastasis Tumor BiomarkersR01CA167967 · NCI · SAINT JOHN'S CANCER INSTITUTE · PI HOON, DAVE S B · 2013 to 2017
$1.9M
Phosphoinositide Signaling Regulates MelanogenesisR01AR063116 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GANESAN, ANAND K · 2013 to 2017
$1.8M
NCATS NIH HHS KL2 TR001416NCATS NIH HHS UL1 TR001414NCI NIH HHS P30 CA062203NCI NIH HHS R01 CA167967NIAMS NIH HHS R01 AR063116
6 · The paper itself

Abstract

Genes and pathways that allow cells to cope with oncogene-induced stress represent selective cancer therapeutic targets that remain largely undiscovered. In this study, we identify a RhoJ signaling pathway that is a selective therapeutic target for BRAF mutant cells. RhoJ deletion in BRAF mutant melanocytes modulates the expression of the pro-apoptotic protein BAD as well as genes involved in cellular metabolism, impairing nevus formation, cellular transformation, and metastasis. Short-term treatment of nascent melanoma tumors with PAK inhibitors that block RhoJ signaling halts the growth of BRAF mutant melanoma tumors in vivo and induces apoptosis in melanoma cells in vitro via a BAD-dependent mechanism. As up to 50% of BRAF mutant human melanomas express high levels of RhoJ, these studies nominate the RhoJ-BAD signaling network as a therapeutic vulnerability for fledgling BRAF mutant human tumors.

Indexed as

Apoptosisbcl-Associated Death ProteinCell Line, TumorCell Transformation, NeoplasticEnzyme InhibitorsGene Expression Regulation, NeoplasticHumansMelanocytesMelanomaMutationNeoplasm MetastasisNevusp21-Activated KinasesProto-Oncogene Proteins B-rafrho GTP-Binding ProteinsSignal TransductionBAD protein, humanbcl-Associated Death ProteinBRAF protein, humanEnzyme Inhibitorsp21-Activated KinasesProto-Oncogene Proteins B-rafrho GTP-Binding ProteinsRHOJ protein, human

Identifiers

PMID28753606
PMCPMC5549996
OpenAlexW2739670623

What OpenQuestion holds

Textmetadata
LicenceCC0
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.