Evidence map›Paper›PMID 30026510›Full record

ArticleScientific reports2018

The lincRNA MIRAT binds to IQGAP1 and modulates the MAPK pathway in NRAS mutant melanoma.

Martina Sanlorenzo, Igor Vujic, Rosaura Esteve-Puig, Kevin Lai, Marin Vujic, Kevin Lin, Christian Posch, Michelle Dimon, Adrian Moy, Mitchell Zekhtser and 9 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

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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

19 authors at 2 institutions in 3 countries.

Martina SanlorenzoUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Igor VujicUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Rosaura Esteve-PuigUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.ORCID 0000-0003-0547-1752
Kevin LaiUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Marin VujicUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.ORCID 0000-0003-4850-0330
Kevin LinUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Christian PoschUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.ORCID 0000-0003-0296-3567
Michelle DimonUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Adrian MoyUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Mitchell ZekhtserUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Katia JohnstonUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Deborah GhoUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Wilson HoUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Abhinay GajjalaUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA.
Juan Oses PrietoDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of California San Francisco - San Francisco, 94115, California, USA.ORCID 0000-0003-4759-2341
Alma BurlingameDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of California San Francisco - San Francisco, 94115, California, USA.
Adil DaudUniversity of California-San Francisco, Mt Zion Cancer Research Center San Francisco, 94115, California, USA.ORCID 0000-0002-6617-8421
Klemens RappersbergerDepartment of Oncology, University of Turin, Torino, 10124, Italy.
Susana Ortiz-UrdaUniversity of California San Francisco, Department of Dermatology, Mt. Zion Cancer Research Center, 2340 Sutter Street, N461, 94115, San Francisco, USA. susana.ortiz@ucsf.edu.
University of California, San Francisco · USSigmund Freud Privatuniversität Wien · AT

Funding

Bio-Organic Biomedical Mass Spectromy ResourceP41GM103481 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BURLINGAME, ALMA L · 2012 to 2015
$6.4M
Role of KIT in Early Melanoma DevelopmentK08CA155035 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ORTIZ URDA, SUSANA · 2011 to 2015
$610k
NCI NIH HHS K08 CA155035NIGMS NIH HHS P41 GM103481
6 · The paper itself

Abstract

Despite major advances in targeted melanoma therapies, drug resistance limits their efficacy. Long noncoding RNAs (lncRNAs) are transcriptome elements that do not encode proteins but are important regulatory molecules. LncRNAs have been implicated in cancer development and response to different therapeutics and are thus potential treatment targets; however, the majority of their functions and molecular interactions remain unexplored. In this study, we identify a novel cytoplasmic intergenic lincRNA (MIRAT), which is upregulated following prolonged MAPK inhibition in NRAS mutant melanoma and modulates MAPK signaling by binding to the MEK scaffold protein IQGAP1. Collectively, our results present MIRAT's direct modulatory effect on the MAPK pathway and highlight the relevance of cytoplasmic lncRNAs as potential targets in drug resistant cancer.

Indexed as

Drug Resistance, NeoplasmMutationCell Line, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticGTP PhosphohydrolasesHumansMAP Kinase Signaling SystemMelanomaMembrane ProteinsProtein Kinase Inhibitorsras GTPase-Activating ProteinsRNA, Long NoncodingSequence Analysis, RNASmall Molecule LibrariesUp-RegulationGTP PhosphohydrolasesIQ motif containing GTPase activating protein 1Membrane ProteinsNRAS protein, humanProtein Kinase Inhibitorsras GTPase-Activating ProteinsRNA, Long NoncodingSmall Molecule Libraries

Identifiers

PMID30026510
PMCPMC6053443
OpenAlexW2883591129

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.