Evidence map›Paper›PMID 39677662›Full record

ArticlebioRxiv : the preprint server for biology2024

IFNγ-dependent metabolic reprogramming restrains an immature, pro-metastatic lymphatic state in melanoma.

Triantafyllia Karakousi, Vanessa Cristaldi, Maria Luiza Lopes de Oliveira, Luiz Henrique Medeiros Geraldo, Tania J González-Robles, Gabrielle da Silva, Alec P Breazeale, Joel Encarnacion-Rosado, Joanna Pozniak, Alec C Kimmelman and 4 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Triantafyllia KarakousiRonald O Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY, USA.
Vanessa CristaldiRonald O Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY, USA.
Maria Luiza Lopes de OliveiraRonald O Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY, USA.
Luiz Henrique Medeiros GeraldoRonald O Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY, USA.
Tania J González-RoblesInstitute of Systems Genetics, Department of Precision Medicine, NYU Grossman School of Medicine, New York, NY USA.
Gabrielle da SilvaRonald O Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY, USA.
Alec P BreazealeDepartment of Cell, Developmental, & Cancer Biology, Oregon Health & Science University, Portland, OR, USA.
Joel Encarnacion-RosadoDepartment of Radiation Oncology, New York University Grossman School of Medicine, New York, NY, USA.
Joanna PozniakLaboratory for Molecular Cancer Biology, Center for Cancer Biology, VIB, Leuven, Belgium.
Alec C KimmelmanDepartment of Cell, Developmental, & Cancer Biology, Oregon Health & Science University, Portland, OR, USA.
Kelly V RugglesInstitute of Systems Genetics, Department of Precision Medicine, NYU Grossman School of Medicine, New York, NY USA.
J Chris MarineLaboratory for Molecular Cancer Biology, Center for Cancer Biology, VIB, Leuven, Belgium.
Navdeep S ChandelFeinberg School of Medicine, Northwestern University, Chicago, IL USA.
Amanda W LundRonald O Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, NY, USA.ORCID 0000-0001-7389-9983

Funding

Project 3: The Evolving Role of Regional Lymph Nodes in Melanoma ProgressionU54CA263001 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Kelly Valentine Ruggles · 2022 to 2026
$11.6M
Training Program in Cell BiologyT32GM136542 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SMITH, SUSAN · 2020 to 2024
$3.0M
Investigating T Cell Egress via Lymphatic Vessels in MelanomaR01CA238163 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI LUND, AMANDA W. · 2019 to 2023
$1.9M
NCI NIH HHS R01 CA238163NCI NIH HHS U54 CA263001NIGMS NIH HHS T32 GM136542
6 · The paper itself

Abstract

Lymphatic vessels play a crucial role in activating anti-tumor immune surveillance but also contribute to metastasis and systemic tumor progression. Whether distinct lymphatic phenotypes exist that govern the switch between immunity and metastasis remains unclear. Here we reveal that cytotoxic immunity normalizes lymphatic function and uncouples immune and metastatic potential. We find that in mice and humans, intratumoral lymphatic vessel density negatively correlates with productive cytotoxic immune responses and identify IFNγ as an intrinsic inhibitor of lymphangiogenesis. Specific deletion of the

Indexed as

immune surveillancelymphangiogenesismelanomametastasis

Identifiers

PMID39677662
PMCPMC11642899

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.