Evidence map›Paper›PMID 32087194›Full record

ArticleThe Journal of investigative dermatology2020

TERT, BRAF, and NRAS Mutational Heterogeneity between Paired Primary and Metastatic Melanoma Tumors.

Gregory A Chang, Jennifer M Wiggins, Broderick C Corless, Mahrukh M Syeda, Jyothirmayee S Tadepalli, Shria Blake, Nathaniel Fleming, Farbod Darvishian, Anna Pavlick, Russell Berman and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Tumor miRNA Signatures Associate with Outcomes of Patients with Stage II/III Melanoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  5. Article
  6. Heliyon · 2023
    Article
  7. New Insights into Melanoma Tumor Syndromes.JID innovations : skin science from molecules to population health · 2022
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Cell-Free DNA in Dermatology Research.The Journal of investigative dermatology · 2022
    Article
  13. Comparison of Two Rapid Assays for the Detection ofDiagnostics (Basel, Switzerland) · 2022
    Article
  14. BRAF Heterogeneity in Melanoma.Current treatment options in oncology · 2021
    Review
  15. Clinical Implications of Acquired BRAF Inhibitors Resistance in Melanoma.International journal of molecular sciences · 2020
    Review
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 2 countries.

Gregory A ChangThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, NYU Langone Health, New York, USA; The Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA; St. Georges University School of Medicine, Grenada, West Indies.
Jennifer M WigginsThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, NYU Langone Health, New York, USA; The Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA.
Broderick C CorlessThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, NYU Langone Health, New York, USA; The Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA; Weill Cornell Medicine Graduate School of Medical Sciences, New York, USA.
Mahrukh M SyedaThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, NYU Langone Health, New York, USA; The Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA.
Jyothirmayee S TadepalliThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, NYU Langone Health, New York, USA; The Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA.
Shria BlakeMolecularMD Corporation, Portland, Oregon, USA.
Nathaniel FlemingThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, NYU Langone Health, New York, USA; The Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA.
Farbod DarvishianThe Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA; Department of Pathology, New York University School of Medicine, NYU Langone Health, New York, USA.
Anna PavlickThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, NYU Langone Health, New York, USA; The Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA; Division of Medical Oncology, Department of Medicine, New York University School of Medicine, NYU Langone Health, New York, USA.
Russell BermanThe Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA; Department of Surgery, New York University School of Medicine, NYU Langone Health, New York, USA.
Richard ShapiroThe Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA; Department of Surgery, New York University School of Medicine, NYU Langone Health, New York, USA.
Yongzhao ShaoThe Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA; Department of Population Health, New York University School of Medicine, NYU Langone Health, New York, USA.
George Karlin-NeumannBio-Rad Laboratories, Hercules, California, USA.
Cindy SpittleMolecularMD Corporation, Portland, Oregon, USA.
Iman OsmanThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, NYU Langone Health, New York, USA; The Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA; Division of Medical Oncology, Department of Medicine, New York University School of Medicine, NYU Langone Health, New York, USA.
David PolskyThe Ronald O. Perelman Department of Dermatology, New York University School of Medicine, NYU Langone Health, New York, USA; The Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, USA. Electronic address: david.polsky@nyumc.org.
NYU Langone Health · USSunEdison (United States) · USBio-Rad (United States) · USCornell University · USSt. George's University · GD

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Project 4P50CA225450 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI OSMAN, IMAN, WEBER, JEFFREY S · 2019 to 2025
$12.5M
Cutaneous Biology and Skin Disease Training ProgramT32AR064184 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ORLOW, SETH J. · 2014 to 2024
$2.1M
Blood-based detection of BRAF and NRAS DNA as biomarkers in patients with stage IU01FD004203 · FDA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI POLSKY, DAVID · 2011 to 2013
$1.1M
Evaluation of TERT promoter mutations as melanoma biomarkers in tumors and plasmaR21CA198495 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI POLSKY, DAVID · 2015 to 2016
$406k
Blood-based detection of BRAF DNA as a biomarker in metastatic melanoma patientsR21CA154786 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI POLSKY, DAVID · 2011 to 2012
$404k
FDA HHS U01 FD004203NCI NIH HHS P30 CA016087NCI NIH HHS P50 CA225450NCI NIH HHS R21 CA154786NCI NIH HHS R21 CA198495NIAMS NIH HHS T32 AR064184
6 · The paper itself

Abstract

Mutational heterogeneity can contribute to therapeutic resistance in solid cancers. In melanoma, the frequencies of intertumoral and intratumoral heterogeneity are controversial. We examined mutational heterogeneity within individual patients with melanoma using multiplatform analysis of commonly mutated driver and nonpassenger genes. We analyzed paired primary and metastatic tumors from 60 patients and multiple metastatic tumors from 39 patients whose primary tumors were unavailable (n = 271 tumors). We used a combination of multiplex SNaPshot assays, Sanger sequencing, mutation-specific PCR, or droplet digital PCR to determine the presence of BRAF

Indexed as

Antineoplastic AgentsDNA Mutational AnalysisDrug Resistance, NeoplasmFemaleGenetic HeterogeneityGTP PhosphohydrolasesHumansLongitudinal StudiesMaleMelanomaMembrane ProteinsMiddle AgedMutationNeoplasms, Second PrimaryProspective StudiesProto-Oncogene Proteins B-rafAntineoplastic AgentsBRAF protein, humanGTP PhosphohydrolasesMembrane ProteinsNRAS protein, humanProto-Oncogene Proteins B-rafTelomeraseTERT protein, human

Identifiers

PMID32087194
PMCPMC7387168
OpenAlexW3008560653

What OpenQuestion holds

Textmetadata
LicenceTDM
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.