Evidence map›Paper›PMID 35582302›Full record

ReviewCancer drug resistance (Alhambra, Calif.)2021

Emerging RAS-directed therapies for cancer.

Michael Conroy, Darren Cowzer, Walter Kolch, Austin G Duffy

Open access · diamondAbstract readReview
In one paragraph

Review in Cancer drug resistance (Alhambra, Calif.), 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
1.4field-weighted citation impact, top 19% 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, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Case Report: Sequential postzygoticFrontiers in genetics · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Recent advances in tumor-targeting chemotherapy drugs.Cancer drug resistance (Alhambra, Calif.) · 2021
    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

4 authors at 2 institutions in 1 country.

Michael ConroyDepartment of Medical Oncology, Mater Misericordiae University Hospital, Dublin 7, Ireland.
Darren CowzerDepartment of Medical Oncology, Mater Misericordiae University Hospital, Dublin 7, Ireland.
Walter KolchSystems Biology Ireland, School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
Austin G DuffyDepartment of Medical Oncology, Mater Misericordiae University Hospital, Dublin 7, Ireland.
Mater Misericordiae University Hospital · IEUniversity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RAS oncogenes are the most commonly mutated oncogenes in human cancer, and RAS-mutant cancers represent a major burden of human disease. Though these oncogenes were discovered decades ago, recent years have seen major advances in understanding of their structure and function, including the therapeutic and prognostic significance of diverse isoforms. Targeting of these mutations has proven difficult, despite some successes with inhibition of RAS effector signalling. More recently, direct RAS inhibition has been achieved in a trial setting. While this has yet to be translated to everyday clinical practice, this development carries much promise. This review summarizes the diverse approaches that have been taken to RAS inhibition and then focuses on the most recent developments in direct inhibition of KRAS(G12C).

Indexed as

erkinhibitionisoformpancreaticRassignallingtargeted

Identifiers

PMID35582302
PMCPMC9094076
OpenAlexW3153358388

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.