Evidence map›Paper›PMID 31027363›Full record

ReviewCells2019

RAC1 Takes the Lead in Solid Tumors.

Pradip De, Jennifer Carlson Aske, Nandini Dey

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

69 citing papers in PubMed, 108 citations in OpenAlex.

  1. Review
  2. GTP biosynthesis is a therapeutic vulnerability in Rac1-mutant melanoma.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Tumor-derived RAC1Science advances · 2025
    Article
  8. Article
  9. Article
  10. Advances in the study of the relationship betweenFrontiers in cell and developmental biology · 2025
    Review
  11. Article
  12. Article
  13. Assessing the mechanism of fast-cycling cancer-associated mutations of Rac1 small Rho GTPase.Protein science : a publication of the Protein Society · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Identification ofInternational journal of molecular sciences · 2023
    Article
  20. Review

9 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

3 authors at 2 institutions in 1 country.

Pradip DeTranslational Oncology Laboratory, Avera Cancer Institute, Sioux Falls, SD 57105, USA. Pradip.De@avera.org.
Jennifer Carlson AskeTranslational Oncology Laboratory, Avera Cancer Institute, Sioux Falls, SD 57105, USA. Jennifer.Aske@avera.org.ORCID 0000-0001-9405-5464
Nandini DeyTranslational Oncology Laboratory, Avera Cancer Institute, Sioux Falls, SD 57105, USA. Nandini.Dey@avera.org.
University of South Dakota · USAvera Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Three GTPases, RAC, RHO, and Cdc42, play essential roles in coordinating many cellular functions during embryonic development, both in healthy cells and in disease conditions like cancers. We have presented patterns of distribution of the frequency of RAC1-alteration(s) in cancers as obtained from cBioPortal. With this background data, we have interrogated the various functions of RAC1 in tumors, including proliferation, metastasis-associated phenotypes, and drug-resistance with a special emphasis on solid tumors in adults. We have reviewed the activation and regulation of RAC1 functions on the basis of its sub-cellular localization in tumor cells. Our review focuses on the role of RAC1 in cancers and summarizes the regulatory mechanisms, inhibitory efficacy, and the anticancer potential of RAC1-PAK targeting agents.

Indexed as

Cell Line, TumorCell MovementCell ProliferationDrug Resistance, NeoplasmHumansNeoplasmsNeovascularization, Pathologicrac1 GTP-Binding Proteinrac1 GTP-Binding ProteinRAC1 protein, humanRAC1resistancesolid tumorssub-cellular signaling

Identifiers

PMID31027363
PMCPMC6562738
OpenAlexW2941747890

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.