Evidence map›Paper›PMID 35187538›Full record

ArticleCancer research communications2021

HSP70 inhibition blocks adaptive resistance and synergizes with MEK inhibition for the treatment of NRAS-mutant melanoma.

Joshua L D Parris, Thibaut Barnoud, Julia I-Ju Leu, Jessica C Leung, Weili Ma, Nicole A Kirven, Adi Naryana Reddy Poli, Andrew V Kossenkov, Qin Liu, Joseph M Salvino and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer research communications, 2021. 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
0.4field-weighted citation impact, top 40% 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. Article
  2. Article
  3. Targeting ErbB3 and Cellular NADPH/NADPACS chemical biology · 2022
    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

14 authors at 3 institutions in 1 country.

Joshua L D ParrisProgram in Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia PA 19104.
Thibaut BarnoudProgram in Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia PA 19104.
Julia I-Ju LeuDepartment of Genetics, University of Pennsylvania Perelman School of Medicine, Philadelphia PA 19104.
Jessica C LeungProgram in Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia PA 19104.
Weili MaProgram in Immunology, Microenvironment and Metastasis, and The Wistar Institute, Philadelphia PA 19104.
Nicole A KirvenProgram in Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia PA 19104.
Adi Naryana Reddy PoliProgram in Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia PA 19104.
Andrew V KossenkovProgram in Gene Expression and Regulation, The Wistar Institute, Philadelphia PA 19104.
Qin LiuProgram in Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia PA 19104.
Joseph M SalvinoProgram in Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia PA 19104.
Donna L GeorgeDepartment of Genetics, University of Pennsylvania Perelman School of Medicine, Philadelphia PA 19104.
Ashani T WeeraratnaDepartment of Biochemistry and Molecular Biology, Johns Hopkins University, Baltimore MD 21205.
Qing ChenProgram in Immunology, Microenvironment and Metastasis, and The Wistar Institute, Philadelphia PA 19104.
Maureen E MurphyProgram in Molecular and Cellular Oncogenesis, The Wistar Institute, Philadelphia PA 19104.
The Wistar Institute · USUniversity of Pennsylvania · USJohns Hopkins University · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Targeting the MAP and PI3 Kinase Pathways in MelanomaP01CA114046 · NCI · WISTAR INSTITUTE · PI WEERARATNA, ASHANI T · 2008 to 2023
$37.1M
TRAINING PROGRAM IN BASIC CANCER RESEARCHT32CA009171 · NCI · WISTAR INSTITUTE · PI Alessandro Gardini · 1985 to 2026
$15.3M
The ARF Tumor SuppressorR01CA139319 · NCI · WISTAR INSTITUTE · PI MURPHY, MAUREEN E. · 2010 to 2019
$3.9M
Understanding PPARgamma signaling in melanoma brain metastasisR01CA241490 · NCI · WISTAR INSTITUTE · PI CHEN, QING · 2020 to 2024
$2.0M
Integrative Approach to Comprehensive Analysis of High Throughput Data on a Cancer Center LevelR50CA211199 · NCI · WISTAR INSTITUTE · PI Andrew V Kossenkov · 2016 to 2026
$1.6M
Genetics of Tumor Suppression by p53R00CA241367 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BARNOUD, THIBAUT · 2022 to 2024
$747k
Genetics of Tumor Suppression by p53K99CA241367 · NCI · WISTAR INSTITUTE · PI BARNOUD, THIBAUT · 2020 to 2021
$238k
NCI NIH HHS K99 CA241367NCI NIH HHS P01 CA114046NCI NIH HHS P30 CA010815NCI NIH HHS R00 CA241367NCI NIH HHS R01 CA139319NCI NIH HHS R01 CA241490NCI NIH HHS R50 CA211199NCI NIH HHS T32 CA009171
6 · The paper itself

Abstract

NRAS-mutant melanoma is currently a challenge to treat. This is due to an absence of inhibitors directed against mutant NRAS, along with adaptive and acquired resistance of this tumor type to inhibitors in the MAPK pathway. Inhibitors to MEK (mitogen-activated protein kinase kinase) have shown some promise for NRAS-mutant melanoma. In this work we explored the use of MEK inhibitors for NRAS-mutant melanoma. At the same time we investigated the impact of the brain microenvironment, specifically astrocytes, on the response of a melanoma brain metastatic cell line to MEK inhibition. These parallel avenues led to the surprising finding that astrocytes enhance the sensitivity of melanoma tumors to MEK inhibitors (MEKi). We show that MEKi cause an upregulation of the transcription factor ID3, which confers resistance. This upregulation of ID3 is blocked by conditioned media from astrocytes. We show that silencing ID3 enhances the sensitivity of melanoma to MEK inhibitors, thus mimicking the effect of the brain microenvironment. Moreover, we report that ID3 is a client protein of the chaperone HSP70, and that HSP70 inhibition causes ID3 to misfold and accumulate in a detergent-insoluble fraction in cells. We show that HSP70 inhibitors synergize with MEK inhibitors against NRAS-mutant melanoma, and that this combination significantly enhances the survival of mice in two different models of NRAS-mutant melanoma. These studies highlight ID3 as a mediator of adaptive resistance, and support the combined use of MEK and HSP70 inhibitors for the therapy of NRAS-mutant melanoma. SIGNIFICANCE: MEK inhibitors are currently used for NRAS-mutant melanoma, but have shown modest efficacy as single agents. This research shows a synergistic effect of combining HSP70 inhibitors with MEK inhibitors for the treatment of NRAS mutant melanoma.

Indexed as

MelanomaMitogen-Activated Protein Kinase KinasesAnimalsGTP PhosphohydrolasesMembrane ProteinsMiceMutationProtein Kinase InhibitorsTumor MicroenvironmentGTP PhosphohydrolasesMembrane ProteinsMitogen-Activated Protein Kinase KinasesProtein Kinase InhibitorsHSP70ID3MEKMelanomaTargeted Therapy

Identifiers

PMID35187538
PMCPMC8849551
OpenAlexW3207025663

What OpenQuestion holds

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Registered trials

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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.