Evidence map›Paper›PMID 32241802›Full record

ArticleGenes & development2020

Targeted chemotherapy overcomes drug resistance in melanoma.

Jingyin Yue, Roberto Vendramin, Fan Liu, Omar Lopez, Monica G Valencia, Helena Gomes Dos Santos, Gabriel Gaidosh, Felipe Beckedorff, Ezra Blumenthal, Lucia Speroni and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  8. Review
  9. Article
  10. Article
  11. Article
  12. Many Distinct Ways Lead to Drug Resistance inLife (Basel, Switzerland) · 2021
    Review
  13. Nanocarrier-Based Drug Delivery for Melanoma Therapeutics.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Article
  16. 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

13 authors at 2 institutions in 2 countries.

Jingyin Yue *Department of Human Genetics, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Roberto Vendramin *Laboratory for Molecular Cancer Biology, Oncology Department, KULeuven, 3000 Leuven, Belgium.ORCID 0000-0001-7191-4887
Fan LiuDepartment of Biochemistry, University of Miami, Miami, Florida 33136, USA.
Omar LopezDepartment of Human Genetics, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Monica G ValenciaDepartment of Human Genetics, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Helena Gomes Dos SantosDepartment of Human Genetics, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Gabriel GaidoshDepartment of Human Genetics, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Felipe BeckedorffDepartment of Human Genetics, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Ezra BlumenthalDepartment of Human Genetics, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Lucia SperoniDepartment of Human Genetics, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Stephen D NimerDepartment of Biochemistry, University of Miami, Miami, Florida 33136, USA.
Jean-Christophe MarineLaboratory for Molecular Cancer Biology, Oncology Department, KULeuven, 3000 Leuven, Belgium.
Ramin ShiekhattarDepartment of Human Genetics, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
University of Miami · USVIB-KU Leuven Center for Cancer Biology · BE

Funding

Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Yan Guo · 2019 to 2026
$24.1M
Enhancer RNA TherapyDP1CA228041 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI SHIEKHATTAR, RAMIN · 2017 to 2021
$5.4M
Elucidation of Integrator's FunctionR01GM078455 · NIGMS · WISTAR INSTITUTE · PI SHIEKHATTAR, RAMIN · 2010 to 2025
$5.1M
Non-coding RNAs in Transcription and Chromatin ArchitectureR01GM105754 · NIGMS · WISTAR INSTITUTE · PI SHIEKHATTAR, RAMIN · 2014 to 2017
$1.7M
NCI NIH HHS DP1 CA228041NCI NIH HHS P30 CA240139NIGMS NIH HHS R01 GM078455NIGMS NIH HHS R01 GM105754
6 · The paper itself

Abstract

The emergence of drug resistance is a major obstacle for the success of targeted therapy in melanoma. Additionally, conventional chemotherapy has not been effective as drug-resistant cells escape lethal DNA damage effects by inducing growth arrest commonly referred to as cellular dormancy. We present a therapeutic strategy termed "targeted chemotherapy" by depleting protein phosphatase 2A (PP2A) or its inhibition using a small molecule inhibitor (1,10-phenanthroline-5,6-dione [phendione]) in drug-resistant melanoma. Targeted chemotherapy induces the DNA damage response without causing DNA breaks or allowing cellular dormancy. Phendione treatment reduces tumor growth of BRAF

Indexed as

Antineoplastic AgentsCell Line, TumorCell ProliferationDNA DamageDrug Resistance, NeoplasmHumansMelanomaProtein Phosphatase 2PyrazolesAntineoplastic AgentsphenidoneProtein Phosphatase 2Pyrazolescellular dormancyDNA damage responsedrug resistanceMAP kinase signalingprotein phosphatase 2Asmall molecule inhibitor

Identifiers

PMID32241802
PMCPMC7197350
OpenAlexW3014753106

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.