Evidence map›Paper›PMID 32344731›Full record

ReviewInternational journal of molecular sciences2020

CDKs in Sarcoma: Mediators of Disease and Emerging Therapeutic Targets.

Jordan L Kohlmeyer, David J Gordon, Munir R Tanas, Varun Monga, Rebecca D Dodd, Dawn E Quelle

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
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  12. CDK4/6-MEK Inhibition in MPNSTs Causes Plasma Cell Infiltration, Sensitization to PD-L1 Blockade, and Tumor Regression.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
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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

6 authors at 1 institution in 1 country.

Jordan L KohlmeyerMolecular Medicine Graduate Program, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
David J GordonThe Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0003-1830-4371
Munir R TanasThe Department of Pathology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Varun MongaThe Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0002-1185-5448
Rebecca D DoddThe Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Dawn E QuelleMolecular Medicine Graduate Program, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Jon C.D. Houtman · 2000 to 2026
$70.0M
Project 4: New Approaches to Improving the Effectiveness of Radionuclide Targeted Treatments in Neuroendocrine TumorsP50CA174521 · NCI · UNIVERSITY OF IOWA · PI MENDA, YUSUF · 2015 to 2021
$13.2M
Predoctoral Training in the Pharmacological SciencesT32GM067795 · NIGMS · UNIVERSITY OF IOWA · PI STRACK, STEFAN · 2004 to 2021
$3.4M
Children's Tumor Foundation 2019 Young Investigator AwardHolden Comprehensive Cancer Center, University of Iowa Mezhir Research AwardNCI NIH HHS P30 CA086862NCI NIH HHS P50 CA174521NIGMS NIH HHS T32 GM067795
6 · The paper itself

Abstract

Sarcomas represent one of the most challenging tumor types to treat due to their diverse nature and our incomplete understanding of their underlying biology. Recent work suggests cyclin-dependent kinase (CDK) pathway activation is a powerful driver of sarcomagenesis. CDK proteins participate in numerous cellular processes required for normal cell function, but their dysregulation is a hallmark of many pathologies including cancer. The contributions and significance of aberrant CDK activity to sarcoma development, however, is only partly understood. Here, we describe what is known about CDK-related alterations in the most common subtypes of sarcoma and highlight areas that warrant further investigation. As disruptions in CDK pathways appear in most, if not all, subtypes of sarcoma, we discuss the history and value of pharmacologically targeting CDKs to combat these tumors. The goals of this review are to (1) assess the prevalence and importance of CDK pathway alterations in sarcomas, (2) highlight the gap in knowledge for certain CDKs in these tumors, and (3) provide insight into studies focused on CDK inhibition for sarcoma treatment. Overall, growing evidence demonstrates a crucial role for activated CDKs in sarcoma development and as important targets for sarcoma therapy.

Indexed as

Age FactorsAnimalsAntineoplastic AgentsBiomarkersCell CycleCyclin-Dependent KinasesDisease SusceptibilityGene Expression Regulation, NeoplasticHumansModels, BiologicalMolecular Targeted TherapyProtein Kinase InhibitorsSarcomaSignal TransductionTranscription, GeneticAntineoplastic AgentsBiomarkersCyclin-Dependent KinasesProtein Kinase InhibitorsCDK inhibitorscell cyclecyclin-dependent kinaseretinoblastoma proteinsarcomatherapeutics

Identifiers

PMID32344731
PMCPMC7215455
OpenAlexW3018801440

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.