Evidence map›Paper›PMID 33016647›Full record

ArticleCancer medicine2020

Molecular and immunological associations of elevated serum lactate dehydrogenase in metastatic melanoma patients: A fresh look at an old biomarker.

Grant M Fischer, Fernando C L Carapeto, Aron Y Joon, Lauren E Haydu, Huiqin Chen, Fuchenchu Wang, John S Van Arnam, Jennifer L McQuade, Khalida Wani, John M Kirkwood and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 14 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

18 authors at 3 institutions in 2 countries.

Grant M FischerDepartments of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0003-3730-9004
Fernando C L CarapetoDepartments of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Aron Y JoonBiostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Lauren E HayduSurgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Huiqin ChenBiostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Fuchenchu WangBiostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
John S Van ArnamDepartments of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jennifer L McQuadeMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Khalida WaniDepartments of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
John M KirkwoodUniversity of Pittsburgh Medical Center, Pittsburgh, PA, USA.
John F ThompsonMelanoma Institute of Australia, The University of Sydney, North Sydney, NSW, Australia.
Michael T TetzlaffDepartments of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Alexander J LazarDepartments of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-6395-4499
Hussein A TawbiMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jeffrey E GershenwaldSurgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Richard A ScolyerMelanoma Institute of Australia, The University of Sydney, North Sydney, NSW, Australia.
Georgina V LongMelanoma Institute of Australia, The University of Sydney, North Sydney, NSW, Australia.
Michael A DaviesDepartments of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-0977-0912
The University of Texas MD Anderson Cancer Center · USThe University of Sydney · AUUniversity of Pittsburgh Medical Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Center for Clinical and Translational Sciences (CCTS)UL1TR000371 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$13.4M
The University of Texas MD Anderson Cancer Center SPORE in MelanomaP50CA221703 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DAVIES, MICHAEL · 2019 to 2023
$10.3M
TRAINING FOR ACADEMIC ONCOLOGY/HEMATOLOGYT32CA009666 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Michael Davies, Courtney DiNardo · 1994 to 2026
$9.8M
Efficacy of combined inhibition of BRAF, MEK, and FAK in melanoma patient derived xenograftsR01CA121118 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Sheri L Holmen · 2007 to 2026
$4.7M
Center for Clinical and Translational Sciences (CCTS)TL1TR000369 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$1.9M
NCATS NIH HHS TL1 TR000369NCATS NIH HHS UL1 TR000371NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA221703NCI NIH HHS R01 CA121118NCI NIH HHS T32 CA009666
6 · The paper itself

Abstract

Elevated serum lactate dehydrogenase (sLDH) is associated with poor clinical outcomes in patients with stage IV metastatic melanoma (MM). It is currently unknown if sLDH elevation correlates with distinct molecular, metabolic, or immune features of melanoma metastases. The identification of such features may identify rational therapeutic strategies for patients with elevated sLDH. Thus, we obtained sLDH levels for melanoma patients with metastases who had undergone molecular and/or immune profiling. Our analysis of multi-omics data from independent cohorts of melanoma metastases showed that elevated sLDH was not significantly associated with differences in immune cell infiltrate, point mutations, DNA copy number variations, promoter methylation, RNA expression, or protein expression in melanoma metastases. The only significant association observed for elevated sLDH was with the number of metastatic sites of disease. Our data support that sLDH correlates with disease burden, but not specific molecular or immunological phenotypes, in metastatic melanoma.

Indexed as

Biomarkers, TumorDatabases, Nucleic AcidGene Expression ProfilingHumansImmunohistochemistryL-Lactate DehydrogenaseMelanomaPrognosisSkin NeoplasmsTissue Array AnalysisUp-RegulationBiomarkers, TumorL-Lactate Dehydrogenasemelanomamolecular profilingserum lactate dehydrogenasetumor immunitytumor metabolism

Identifiers

PMID33016647
PMCPMC7666738
OpenAlexW3091360746

What OpenQuestion holds

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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.