Evidence map›Paper›PMID 36861094›Full record

ArticleCancer research communications2022

Characterization of Novel Derivatives of MBQ-167, an inhibitor of the GTP-binding proteins Rac/Cdc42.

Julia I Medina, Ailed Cruz-Collazo, Maria Del Mar Maldonado, Tatiana Matos Gascot, Luis D Borrero-Garcia, Mariana Cooke, Marcelo G Kazanietz, Eliud Hernandez O'Farril, Cornelis P Vlaar, Suranganie Dharmawardhane

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Cancer research communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06075810 (A Phase 1 Open-Label, First-in-Human Trial of Oral MBQ-167 as Single Agent in Participants With Advanced Breast Cancer), which is not on this map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 20% 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.

NCT06075810 phase1recruitingnot on this mapstarted 2023, after this paper: background citation

A Phase 1 Open-Label, First-in-Human Trial of Oral MBQ-167 as Single Agent in Participants With Advanced Breast Cancer

TypeinterventionalSponsorMBQ PharmaRan2023 to 2025Enrolled48ConditionsBreast Cancer, Breast Neoplasm, Breast Cancer Stage IVArmsMBQ-167
3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cancers · 2025
    Article
  10. Article
  11. Review
  12. RAC1 signaling in prostate cancer: VAV GEFs take center stage.Frontiers in cell and developmental biology · 2025
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. 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

10 authors at 3 institutions in 2 countries.

Julia I MedinaDepartment of Biochemistry, School of Medicine, University of Puerto Rico, San Juan, PR.
Ailed Cruz-CollazoDepartment of Biochemistry, School of Medicine, University of Puerto Rico, San Juan, PR.
Maria Del Mar MaldonadoDepartment of Biochemistry, School of Medicine, University of Puerto Rico, San Juan, PR.
Tatiana Matos GascotDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Puerto Rico, San Juan, PR.
Luis D Borrero-GarciaMBQ Pharma, Inc., San Juan, PR.
Mariana CookeDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Marcelo G KazanietzDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Eliud Hernandez O'FarrilDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Puerto Rico, San Juan, PR.
Cornelis P VlaarDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Puerto Rico, San Juan, PR.
Suranganie DharmawardhaneDepartment of Biochemistry, School of Medicine, University of Puerto Rico, San Juan, PR.
University of Puerto Rico System · PRTranslational Therapeutics (United States) · USPuerto Rico Department of Health · PR

Funding

RISE Option III: MBRS RISE at the UPR Medical Sciences CampusR25GM061838 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI CADILLA, CARMEN LYDIA · 2000 to 2021
$25.5M
Cancer Prevention and Control (CAPAC) Research Training ProgramR25CA240120 · NCI · COMPREHENSIVE CANCER CENTER/ UNIV/PR · PI ANA Patricia ORTIZ, Marievelisse Soto-Salgado · 2019 to 2026
$2.8M
Rac guanine nucleotide exchange factors in lung cancerR01CA265999 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KAZANIETZ, MARCELO G. · 2022 to 2025
$2.3M
Targeting breast cancer progressionSC3GM084824 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI DHARMAWARDHANE, SURANGANIE · 2008 to 2021
$1.6M
Towards the Development of Novel Vav-Rac InhibitorsSC3GM116713 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI VLAAR, CORNELIS P · 2016 to 2019
$450k
NCI NIH HHS R01 CA265999NCI NIH HHS R25 CA240120NIGMS NIH HHS R25 GM061838NIGMS NIH HHS SC3 GM084824NIGMS NIH HHS SC3 GM116713
6 · The paper itself

Abstract

Rac and Cdc42, are homologous GTPases that regulate cell migration, invasion, and cell cycle progression; thus, representing key targets for metastasis therapy. We previously reported on the efficacy of MBQ-167, which blocks both Rac1 and Cdc42 in breast cancer cells and mouse models of metastasis. To identify compounds with increased activity, a panel of MBQ-167 derivatives was synthesized, maintaining its 9-ethyl-3-(1

Indexed as

GTP-Binding Proteinsrac GTP-Binding ProteinsAnimalsCell DivisionCell MovementGuanine Nucleotide Exchange FactorsMiceGTP-Binding ProteinsGuanine Nucleotide Exchange Factorsrac GTP-Binding ProteinsCdc42MBQ-167 derivativesmetastatic breast cancerRacRac/Cdc42 inhibitors

Identifiers

PMID36861094
PMCPMC9970268
OpenAlexW4311815250

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.