Evidence map›Paper›PMID 31940493›Full record

ArticleCell reports2020

FOXD3 Regulates VISTA Expression in Melanoma.

Sheera R Rosenbaum, Meghan Knecht, Mehri Mollaee, Zhijiu Zhong, Dan A Erkes, Peter A McCue, Inna Chervoneva, Adam C Berger, Jennifer A Lo, David E Fisher and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

64 citing papers in PubMed, 83 citations in OpenAlex.

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4 more citing papers are in PubMed but not listed here.

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 5 institutions in 1 country.

Sheera R RosenbaumDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Meghan KnechtDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Mehri MollaeeDepartment of Pathology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Zhijiu ZhongSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Dan A ErkesDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Peter A McCueDepartment of Pathology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Inna ChervonevaDivision of Biostatistics in the Department of Pharmacology and Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Adam C BergerSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA; Department of Surgery, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Jennifer A LoDepartment of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
David E FisherDepartment of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Jeffrey E GershenwaldDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Michael A DaviesDepartment of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Timothy J PurwinDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Andrew E AplinDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA; Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA. Electronic address: andrew.aplin@jefferson.edu.
Thomas Jefferson University · USSidney Kimmel Cancer Center · USThe University of Texas MD Anderson Cancer Center · USHarvard University · USMassachusetts General Hospital · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DANIEL P SILVER · 1995 to 2026
$94.8M
Transcriptional mechanisms and melanomaP01CA163222 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DAVID E FISHER · 2013 to 2026
$25.3M
The MITF transcriptional network: melanoma risk and carcinogenesisR01AR043369 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI DAVID E FISHER · 1996 to 2026
$9.4M
Therapeutic strategies for treatment of giant congenital melanocytic neviR01AR072304 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI DAVID E FISHER · 2017 to 2026
$3.9M
Request for Supplemental Funds aligned to CA160495R01CA160495 · NCI · THOMAS JEFFERSON UNIVERSITY · PI APLIN, ANDREW ERIC · 2012 to 2022
$3.6M
A druggable dependency in low-MITF/high-AXL melanoma: preclinical efficacy and mechanism of action in a key treatment-resistant subclass.R01CA222871 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FISHER, DAVID E · 2018 to 2022
$1.8M
Mutant BRAF-regulated transcription factors in melanoma progressionR01CA196278 · NCI · THOMAS JEFFERSON UNIVERSITY · PI APLIN, ANDREW ERIC · 2015 to 2019
$1.8M
Training Program in Cellular, Biochemical, and Molecular SciencesT32GM100836 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI BENOVIC, JEFFREY L · 2012 to 2016
$809k
Tumor Intrinsic Regulation of Immune Evasion Pathways in MelanomaF99CA245552 · NCI · THOMAS JEFFERSON UNIVERSITY · PI ROSENBAUM, SHEERA · 2019 to 2020
$92k
NCI NIH HHS F99 CA245552NCI NIH HHS P01 CA163222NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA056036NCI NIH HHS R01 CA160495NCI NIH HHS R01 CA196278NCI NIH HHS R01 CA222871NIAMS NIH HHS R01 AR043369NIAMS NIH HHS R01 AR072304NIGMS NIH HHS T32 GM100836
6 · The paper itself

Abstract

Immune checkpoint inhibitors have improved patient survival in melanoma, but the innate resistance of many patients necessitates the investigation of alternative immune targets. Many immune checkpoint proteins lack proper characterization, including V-domain Ig suppressor of T cell activation (VISTA). VISTA expression on immune cells can suppress T cell activity; however, few studies have investigated its expression and regulation in cancer cells. In this study, we observe that VISTA is expressed in melanoma patient samples and cell lines. Tumor cell-specific expression of VISTA promotes tumor onset in vivo, associated with increased intratumoral T regulatory cells, and enhanced PDL-1 expression on tumor-infiltrating macrophages. VISTA transcript levels are regulated by the stemness factor Forkhead box D3 (FOXD3). BRAF inhibition upregulates FOXD3 and reduces VISTA expression. Overall, this study demonstrates melanoma cell expression of VISTA and its regulation by FOXD3, contributing to the rationale for therapeutic strategies that combine targeted inhibitors with immune checkpoint blockade.

Indexed as

AdultAgedAged, 80 and overAnimalsB7 AntigensCell Line, TumorFemaleForkhead Transcription FactorsHumansLymphocytes, Tumor-InfiltratingMaleMelanomaMelanoma, ExperimentalMiceMice, Inbred C57BLMice, Inbred NODB7 AntigensForkhead Transcription FactorsFOXD3 protein, humanProto-Oncogene Proteins B-rafRNA, MessengerVSIR protein, humanDD1αDies1FOXD3immune checkpointPD-1HVISTAVSIR

Identifiers

PMID31940493
PMCPMC6995351
OpenAlexW2999762186

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.