Evidence map›Paper›PMID 36675167›Full record

ReviewInternational journal of molecular sciences2023

A Focused Review of Ras Guanine Nucleotide-Releasing Protein 1 in Immune Cells and Cancer.

Tu Chun Hsu, Gisele O L Rodrigues, Hila Winer, Julie A Hixon, Wenqing Li, Nadya I Tarasova, Scott K Durum

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. NK cells in HPV-related tumorigenesis: mechanisms and clinical applications.Frontiers in cellular and infection microbiology · 2025
    Review
  12. Article
  13. Editorial for the Special Issue "Molecular Mechanism of Leukemia".International journal of molecular sciences · 2023
    Article
  14. Article
  15. 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

7 authors at 2 institutions in 1 country.

Tu Chun HsuCytokines and Immunity Section, Cancer Innovation Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.ORCID 0000-0001-7591-530X
Gisele O L RodriguesCytokines and Immunity Section, Cancer Innovation Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.ORCID 0000-0002-8526-2258
Hila WinerCytokines and Immunity Section, Cancer Innovation Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.ORCID 0000-0002-1064-0154
Julie A HixonCytokines and Immunity Section, Cancer Innovation Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.ORCID 0000-0002-6505-2392
Wenqing LiCytokines and Immunity Section, Cancer Innovation Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.
Nadya I TarasovaCancer Innovation Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA.ORCID 0000-0002-4949-0069
Scott K DurumCytokines and Immunity Section, Cancer Innovation Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.
National Institutes of Health · USNational Cancer Institute · US

Funding

Cytokines and T Cell DevelopmentZIABC009287 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DURUM, SCOTT · 2009 to 2025
$15.5M
Inhibitors of protein-protein interactionsZIABC011306 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TARASOVA, NADYA · 2010 to 2025
$7.3M
6 · The paper itself

Abstract

Four Ras guanine nucleotide-releasing proteins (RasGRP1 through 4) belong to the family of guanine nucleotide exchange factors (GEFs). RasGRPs catalyze the release of GDP from small GTPases Ras and Rap and facilitate their transition from an inactive GDP-bound to an active GTP-bound state. Thus, they regulate critical cellular responses via many downstream GTPase effectors. Similar to other RasGRPs, the catalytic module of RasGRP1 is composed of the Ras exchange motif (REM) and Cdc25 domain, and the EF hands and C1 domain contribute to its cellular localization and regulation. RasGRP1 can be activated by a diacylglycerol (DAG)-mediated membrane recruitment and protein kinase C (PKC)-mediated phosphorylation. RasGRP1 acts downstream of the T cell receptor (TCR), B cell receptors (BCR), and pre-TCR, and plays an important role in the thymocyte maturation and function of peripheral T cells, B cells, NK cells, mast cells, and neutrophils. The dysregulation of RasGRP1 is known to contribute to numerous disorders that range from autoimmune and inflammatory diseases and schizophrenia to neoplasia. Given its position at the crossroad of cell development, inflammation, and cancer, RASGRP1 has garnered interest from numerous disciplines. In this review, we outline the structure, function, and regulation of RasGRP1 and focus on the existing knowledge of the role of RasGRP1 in leukemia and other cancers.

Indexed as

Guanine Nucleotide Exchange FactorsImmune SystemNeoplasmsDNA-Binding ProteinsGuanine NucleotidesHumansReceptors, Antigen, T-CellT-LymphocytesDNA-Binding ProteinsGuanine Nucleotide Exchange FactorsGuanine NucleotidesRASGRP1 protein, humanReceptors, Antigen, T-CellcancerleukemiaRasRasGEFRasGRP1

Identifiers

PMID36675167
PMCPMC9864139
OpenAlexW4316372003

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.