Evidence map›Paper›PMID 36028717›Full record

ReviewNature reviews. Clinical oncology2022

The current state of the art and future trends in RAS-targeted cancer therapies.

Salman R Punekar, Vamsidhar Velcheti, Benjamin G Neel, Kwok-Kin Wong

Open access · bronzeAbstract readReview
In one paragraph

Review in Nature reviews. Clinical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 310 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
310citing papers in PubMed, 2 pooled it
49.1field-weighted citation impact, top 1% 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

310 citing papers in PubMed, 2 syntheses or guidelines pooled it, 491 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pancreatic Cancer KRAS Breakthrough: Drug Graveyard No More.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Changes in the transcriptome and synthetic lethal dependencies followingProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. RAS Inhibitor RMC-7977 Blocks Vascular Overgrowth of NRASJournal of cellular and molecular medicine · 2026
    Article
  15. Article
  16. Advances in applications of siRNA in cancer therapy: challenges and opportunities.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  17. Review
  18. Article
  19. Article
  20. Precision Targeting ofInternational journal of molecular sciences · 2026
    Review

250 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

4 authors at 2 institutions in 1 country.

Salman R PunekarDivision of Hematology and Medical Oncology, Department of Medicine, Laura and Isaac Perlmutter Cancer Center, New York University (NYU) Grossman School of Medicine, NYU Langone Health, New York, NY, USA.
Vamsidhar VelchetiDivision of Hematology and Medical Oncology, Department of Medicine, Laura and Isaac Perlmutter Cancer Center, New York University (NYU) Grossman School of Medicine, NYU Langone Health, New York, NY, USA.
Benjamin G NeelDivision of Hematology and Medical Oncology, Department of Medicine, Laura and Isaac Perlmutter Cancer Center, New York University (NYU) Grossman School of Medicine, NYU Langone Health, New York, NY, USA.
Kwok-Kin WongDivision of Hematology and Medical Oncology, Department of Medicine, Laura and Isaac Perlmutter Cancer Center, New York University (NYU) Grossman School of Medicine, NYU Langone Health, New York, NY, USA. Kwok-Kin.Wong@nyulangone.org.ORCID 0000-0001-6323-235X
New York University · USNYU Langone Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite being the most frequently altered oncogenic protein in solid tumours, KRAS has historically been considered 'undruggable' owing to a lack of pharmacologically targetable pockets within the mutant isoforms. However, improvements in drug design have culminated in the development of inhibitors that are selective for mutant KRAS in its active or inactive state. Some of these inhibitors have proven efficacy in patients with KRAS

Indexed as

NeoplasmsProto-Oncogene Proteins p21(ras)HumansMutationSignal TransductionTumor MicroenvironmentProto-Oncogene Proteins p21(ras)

Identifiers

PMID36028717
PMCPMC9412785
OpenAlexW4293176236

What Socratic holds

Textmetadata
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.