Evidence map›Paper›PMID 35223844›Full record

ArticleFrontiers in cell and developmental biology2022

Histone 3 Methyltransferases Alter Melanoma Initiation and Progression Through Discrete Mechanisms.

Sara E DiNapoli, Raúl Martinez-McFaline, Hao Shen, Ashley S Doane, Alexendar R Perez, Akanksha Verma, Amanda Simon, Isabel Nelson, Courtney A Balgobin, Caitlin T Bourque and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

17 authors at 4 institutions in 2 countries.

Sara E DiNapoliDepartment of Surgery, Weill Cornell Medicine, New York, NY, United States.
Raúl Martinez-McFalineDepartment of Surgery, Weill Cornell Medicine, New York, NY, United States.
Hao ShenDivision of Hematology/Oncology, Weill Cornell Medicine, New York, NY, United States.
Ashley S DoaneCaryl and Israel Institute for Precision Medicine, Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, United States.
Alexendar R PerezDepartment of Anesthesia and Perioperative Care, UCSF, San Francisco, CA, United States.
Akanksha VermaCaryl and Israel Institute for Precision Medicine, Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, United States.
Amanda SimonDepartment of Dermatology, Weill Cornell Medicine, New York, NY, United States.
Isabel NelsonDepartment of Surgery, Weill Cornell Medicine, New York, NY, United States.
Courtney A BalgobinDepartment of Surgery, Weill Cornell Medicine, New York, NY, United States.
Caitlin T BourqueDepartment of Surgery, Weill Cornell Medicine, New York, NY, United States.
Jun YaoDepartment of Surgery, Weill Cornell Medicine, New York, NY, United States.
Renuka RamanDepartment of Surgery, Weill Cornell Medicine, New York, NY, United States.
Wendy BéguelinDivision of Hematology/Oncology, Weill Cornell Medicine, New York, NY, United States.
Jonathan H ZippinDepartment of Dermatology, Weill Cornell Medicine, New York, NY, United States.
Olivier ElementoCaryl and Israel Institute for Precision Medicine, Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, United States.
Ari M MelnickDivision of Hematology/Oncology, Weill Cornell Medicine, New York, NY, United States.
Yariv HouvrasDepartment of Surgery, Weill Cornell Medicine, New York, NY, United States.
Weill Cornell Medicine · USCornell University · USLander Institute · ILUniversity of California, San Francisco · US

Funding

Mechanisms of cAMP-dependent regulation of melanosome pHR01AR077664 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI Jonathan Hale Zippin · 2021 to 2026
$3.6M
Uncovering the role of m6A in the melanocyte response to ultraviolet lightR21CA224391 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI JAFFREY, SAMIE R, ZIPPIN, JONATHAN HALE · 2018 to 2019
$399k
NCI NIH HHS R21 CA224391NIAMS NIH HHS R01 AR077664
6 · The paper itself

Abstract

Perturbations to the epigenome are known drivers of tumorigenesis. In melanoma, alterations in histone methyltransferases that catalyze methylation at histone 3 lysine 9 and histone 3 lysine 27-two sites of critical post-translational modification-have been reported. To study the function of these methyltransferases in melanoma, we engineered melanocytes to express histone 3 lysine-to-methionine mutations at lysine 9 and lysine 27, which are known to inhibit the activity of histone methyltransferases, in a zebrafish melanoma model. Using this system, we found that loss of histone 3 lysine 9 methylation dramatically suppressed melanoma formation and that inhibition of histone 3 lysine 9 methyltransferases in human melanoma cells increased innate immune response signatures. In contrast, loss of histone 3 lysine 27 methylation significantly accelerated melanoma formation. We identified

Indexed as

epigeneticshistone 3histone methyl transferase (HMT)melanomazebrafish

Identifiers

PMID35223844
PMCPMC8866878
OpenAlexW4211104450

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.