Evidence map›Paper›PMID 38785960›Full record

ReviewBiomolecules2024

LSD2 Is an Epigenetic Player in Multiple Types of Cancer and Beyond.

Hyun-Min Kim, Zifei Liu

Abstract readReview
In one paragraph

Review in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

2 authors.

Hyun-Min KimDivision of Natural and Applied Sciences, Duke Kunshan University, Kunshan 215316, China.ORCID 0000-0003-4610-3606
Zifei LiuDivision of Natural and Applied Sciences, Duke Kunshan University, Kunshan 215316, China.ORCID 0000-0003-1747-2568

Funding

Kunshan Shuangchuang Grant KSSC202202060
6 · The paper itself

Abstract

Histone demethylases, enzymes responsible for removing methyl groups from histone proteins, have emerged as critical players in regulating gene expression and chromatin dynamics, thereby influencing various cellular processes. LSD2 and LSD1 have attracted considerable interest among these demethylases because of their associations with cancer. However, while LSD1 has received significant attention, LSD2 has not been recognized to the same extent. In this study, we conduct a comprehensive comparison between LSD2 and LSD1, with a focus on exploring LSD2's implications. While both share structural similarities, LSD2 possesses unique features as well. Functionally, LSD2 shows diverse roles, particularly in cancer, with tissue-dependent roles. Additionally, LSD2 extends beyond histone demethylation, impacting DNA methylation, cancer cell reprogramming, E3 ubiquitin ligase activity and DNA damage repair pathways. This study underscores the distinct roles of LSD2, providing insights into their contributions to cancer and other cellular processes.

Indexed as

DNA MethylationEpigenesis, GeneticHistone DemethylasesNeoplasmsDNA RepairF-Box ProteinsGene Expression Regulation, NeoplasticHistonesHumansJumonji Domain-Containing Histone DemethylasesF-Box ProteinsHistone DemethylasesHistonesJumonji Domain-Containing Histone DemethylasesKDM1A protein, humanKDM1B protein, humanKDM2A protein, humanAOF1cancerDNA repairhistone demethylaseKDM1AKDM1BLSD1LSD2

Identifiers

PMID38785960
PMCPMC11118440

What OpenQuestion holds

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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.