Evidence map›Paper›PMID 35538224›Full record

ArticleOncogene2022

Synthetic lethal kinases in Ras/p53 mutant squamous cell carcinoma.

Russell Moser, Kay E Gurley, Olga Nikolova, Guangrong Qin, Rashmi Joshi, Eduardo Mendez, Ilya Shmulevich, Amanda Ashley, Carla Grandori, Christopher J Kemp

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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 6 institutions in 2 countries.

Russell MoserDivision of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Kay E GurleyDivision of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.ORCID 0000-0001-5138-468X
Olga NikolovaDivision of Oncological Sciences, Oregon Health and Science University, Portland, OR, USA.
Guangrong QinInstitute for Systems Biology, Seattle, WA, USA.
Rashmi JoshiNew Mexico State University, Las Cruces, NM, USA.
Eduardo Mendez
Ilya ShmulevichInstitute for Systems Biology, Seattle, WA, USA.
Amanda AshleyNew Mexico State University, Las Cruces, NM, USA.
Carla GrandoriSEngine Precision Medicine, Seattle, WA, USA.
Christopher J KempDivision of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. cjkemp@fhcrc.org.
Fred Hutch Cancer Center · USInstitute for Systems Biology · USNew Mexico State University · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAOregon Health & Science University · USPrecision for Medicine (United States) · US

Funding

Research Education About Cancer and Health (REACH) CoreU54CA132381 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Jean Alison McDougall · 2007 to 2026
$25.3M
Personalized cancer models to discover and develop new therapeutic targets.U01CA217883 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KEMP, CHRISTOPHER J · 2017 to 2021
$4.3M
An integrated computational and functional genomics discovery engine for precliniU01CA176303 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KEMP, CHRISTOPHER J · 2013 to 2016
$4.1M
An Academic-Industry Partnership to Advance Functional Genomics for Personalized Oncology.R01CA214428 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KEMP, CHRISTOPHER J · 2018 to 2022
$3.0M
Exploiting WEE1/p53 synthetic lethality as a novel therapy in head and neck cancerR01CA215647 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI CLURMAN, BRUCE E, KEMP, CHRISTOPHER J · 2017 to 2021
$2.0M
NCI NIH HHS R01 CA214428NCI NIH HHS R01 CA215647NCI NIH HHS U01 CA176303NCI NIH HHS U01 CA217883NCI NIH HHS U54 CA132381
6 · The paper itself

Abstract

The oncogene Ras and the tumor suppressor gene p53 are frequently co-mutated in human cancer and mutations in Ras and p53 can cooperate to generate a more malignant cell state. To discover novel druggable targets for cancers carrying co-mutations in Ras and p53, we performed arrayed, kinome focused siRNA and oncology drug phenotypic screening utilizing a set of syngeneic Ras mutant squamous cell carcinoma (SCC) cell lines that also carried co-mutations in selected p53 pathway genes. These cell lines were derived from SCCs from carcinogen-treated inbred mice which harbored germline deletions or mutations in Trp53, p19

Indexed as

Carcinoma, Squamous Cellras ProteinsTumor Suppressor Protein p53AnimalsCell Line, TumorCyclin-Dependent Kinase Inhibitor p16HumansMiceMutationRNA, Small InterferingCyclin-Dependent Kinase Inhibitor p16ras ProteinsRNA, Small InterferingTrp53 protein, mouseTumor Suppressor Protein p53

Identifiers

PMID35538224
OpenAlexW4229445668

What OpenQuestion 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 OpenQuestion graph.