Evidence map›Paper›PMID 33456709›Full record

ArticleOncotarget2021

Combination therapies for MPNSTs targeting RABL6A-RB1 signaling.

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

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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
  5. Article
  6. Review
  7. Review
  8. Review
  9. RABL6A Regulates Schwann Cell Senescence in an RB1-Dependent Manner.International journal of molecular sciences · 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

7 authors at 1 institution in 1 country.

Jordan L KohlmeyerMolecular Medicine Graduate Program, University of Iowa, Iowa City, Iowa, USA.
David J GordonDepartment of Pediatrics, University of Iowa, Iowa City, Iowa, USA.
Munir R TanasMolecular Medicine Graduate Program, University of Iowa, Iowa City, Iowa, USA.
Rebecca D DoddMolecular Medicine Graduate Program, University of Iowa, Iowa City, Iowa, USA.
Varun MongaDepartment of Internal Medicine, University of Iowa, Iowa City, Iowa, USA.
Benjamin W DarbroDepartment of Pediatrics, University of Iowa, Iowa City, Iowa, USA.
Dawn E QuelleMolecular Medicine Graduate Program, University of Iowa, Iowa City, Iowa, USA.
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 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 ODORISIO, THOMAS · 2015 to 2021
$13.2M
Gene Expression Signature Based Screening in Ewing SarcomaR37CA217910 · NCI · UNIVERSITY OF IOWA · PI GORDON, DAVID J · 2018 to 2024
$2.6M
NCI NIH HHS P30 CA086862NCI NIH HHS P50 CA174521NCI NIH HHS R37 CA217910
6 · The paper itself

Abstract

Precision medicine relies on a detailed molecular understanding of disease pathogenesis. Here, we consider urgently needed therapeutic options for malignant peripheral nerve sheath tumors (MPNSTs) based on emerging insights into druggable pathway alterations found to drive this deadly cancer. Recent observations demonstrate an essential role for an oncogenic GTPase, RABL6A, in promoting MPNST progression through hyperactivation of cyclin-dependent kinases (CDKs) and inactivation of the retinoblastoma (RB1) tumor suppressor. Monotherapies with CDK4/6 inhibitors have shown limited efficacy and durability in pre-clinical studies of MPNSTs and in clinical studies of other tumors. Therefore, we discuss the rationale and clinical benefits of inhibiting multiple RABL6A effectors, particularly CDK4/6 and MEK kinases, in targeted combination therapies suitable for MPNSTs and other Ras-driven malignancies.

Indexed as

CDK4/6 and MEK inhibitorsMPNSTRABL6A-RB1 signalingRastargeted cancer therapy

Identifiers

PMID33456709
PMCPMC7800773
OpenAlexW3119046170

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.