Evidence map›Paper›PMID 37997756›Full record

ArticleExpert opinion on therapeutic targets

Lysine-specific demethylase 1 as a therapeutic cancer target: observations from preclinical study.

Jessica D Johnson, Salvador Alejo, Sridharan Jayamohan, Gangadhara R Sareddy

Open access · greenAbstract read
In one paragraph

Article in Expert opinion on therapeutic targets. 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
1.1field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. [Advances in Targeted Therapy for Malignant Pleural Mesothelioma].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2024
    Review
  3. Review
  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

4 authors at 2 institutions in 1 country.

Jessica D JohnsonDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, TX, USA.
Salvador AlejoDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, TX, USA.
Sridharan JayamohanDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, TX, USA.
Gangadhara R SareddyDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, TX, USA.
The University of Texas Health Science Center at San Antonio · USThe University of Texas Health Science Center at Houston · US

Funding

Cancer Biology Training ProgramT32CA148724 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Pei Wang, Feng-Chun Yang · 2011 to 2026
$3.3M
KDM1A inhibitors as novel therapeutics for glioblastomaR01NS106173 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SAREDDY, GANGADHARA R · 2019 to 2023
$1.6M
NCI NIH HHS T32 CA148724NINDS NIH HHS R01 NS106173
6 · The paper itself

Abstract

introductionLysine-specific histone demethylase 1A (KDM1A/LSD1) has emerged as an important therapeutic target in various cancer types. LSD1 regulates a wide range of biological processes that influence cancer development, progression, metastasis, and therapy resistance. However, recent studies have revealed novel aspects of LSD1 biology, shedding light on its involvement in immunogenicity, antitumor immunity, and DNA damage response. These emerging findings have the potential to be leveraged in the design of effective LSD1-targeted therapies. AREAS COVERED: This paper discusses the latest developments in the field of LSD1 biology, focusing on its role in regulating immunogenicity, antitumor immunity, and DNA damage response mechanisms. The newfound understanding of these mechanisms has opened possibilities for the development of novel LSD1-targeted therapies for cancer treatment. Additionally, the paper provides an overview of LSD1 inhibitor-based combination therapies for the treatment of cancer. EXPERT OPINION: Exploiting LSD1 role in antitumor immunity and DNA damage response provides cues to not only understand the LSD1-resistant mechanisms but also rationally design new combination therapies that are more efficient and less toxic than monotherapy. The exploration of LSD1 biology and the development of LSD1-targeted therapies hold great promise for the future of cancer treatment.

Indexed as

LysineNeoplasmsHistone DemethylasesHumansHistone DemethylasesKDM1A protein, humanLysineantitumor immunitycombination therapiesDNA damage responseDNA repairepigeneticsimmune therapiesLSD1/KDM1A

Identifiers

PMID37997756
PMCPMC10872912
OpenAlexW4388977594

What OpenQuestion holds

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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.