Evidence map›Paper›PMID 34947990›Full record

ReviewInternational journal of molecular sciences2021

Past and Future Strategies to Inhibit Membrane Localization of the KRAS Oncogene.

Malak Haidar, Patrick Jacquemin

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. KRAS4B is required for placental development.Cellular and molecular life sciences : CMLS · 2025
    Article
  6. Article
  7. Article
  8. Revealing KRas4b topology on the membrane surface.Biochemical and biophysical research communications · 2023
    Article
  9. Article
  10. Article
  11. Review
  12. 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

2 authors at 1 institution in 1 country.

Malak HaidarDe Duve Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.
Patrick JacqueminDe Duve Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.
UCLouvain · BE

Funding

Foundation for Cancer Research Belgium 2018-076
6 · The paper itself

Abstract

KRAS is one of the most studied oncogenes. It is well known that KRAS undergoes post-translational modifications at its C-terminal end. These modifications are essential for its membrane location and activity. Despite significant efforts made in the past three decades to target the mechanisms involved in its membrane localization, no therapies have been approved and taken into the clinic. However, many studies have recently reintroduced interest in the development of KRAS inhibitors, either by directly targeting KRAS or indirectly through the inhibition of critical steps involved in post-translational KRAS modifications. In this review, we summarize the approaches that have been applied over the years to inhibit the membrane localization of KRAS in cancer and propose a new anti-KRAS strategy that could be used in clinic.

Indexed as

Antineoplastic AgentsCell MembraneDown-RegulationGene Expression Regulation, NeoplasticHumansMolecular Targeted TherapyNeoplasmsProtein Processing, Post-TranslationalProtein TransportProto-Oncogene Proteins p21(ras)Signal TransductionAntineoplastic AgentsKRAS protein, humanProto-Oncogene Proteins p21(ras)cancerKRASplasma membraneRAS

Identifiers

PMID34947990
PMCPMC8707736
OpenAlexW4200283582

What Socratic 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 Socratic graph.