Evidence map›Paper›PMID 38095719›Full record

ReviewHuman genetics2024

An emerging link between lncRNAs and cancer sex dimorphism.

Ikrame Naciri, Maria D Andrade-Ludena, Ying Yang, Mei Kong, Sha Sun

Open access · hybridAbstract readReview
In one paragraph

Review in Human genetics, 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
1.0field-weighted citation impact, top 20% 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, 4 citations in OpenAlex.

  1. FASEB bioAdvances · 2026
    Article
  2. Article
  3. Loss of XIST lncRNA unlocks stemness and cellular plasticity in ovarian cancer.Proceedings of the National Academy of Sciences of the United States of America · 2024
    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

5 authors at 1 institution in 1 country.

Ikrame NaciriDepartment of Developmental and Cell Biology, School of Biological Sciences, University of California Irvine, Irvine, CA, 92697, USA.
Maria D Andrade-LudenaDepartment of Developmental and Cell Biology, School of Biological Sciences, University of California Irvine, Irvine, CA, 92697, USA.
Ying YangDepartment of Molecular Biology and Biochemistry, School of Biological Sciences, University of California Irvine, Irvine, CA, 92697, USA.
Mei KongDepartment of Molecular Biology and Biochemistry, School of Biological Sciences, University of California Irvine, Irvine, CA, 92697, USA. meik1@uci.edu.ORCID http://orcid.org/0000-0001-8139-2349
Sha SunDepartment of Developmental and Cell Biology, School of Biological Sciences, University of California Irvine, Irvine, CA, 92697, USA. shasun@uci.edu.ORCID http://orcid.org/0000-0002-0044-6403
University of California, Irvine · US

Funding

Using dietary glutamine supplementation for melanoma prevention and targeted therapyR01CA244360 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI KONG, MEI · 2021 to 2025
$2.1M
Elucidating the molecular basis of lncRNA evolution for mammalian dosage compensationR01GM141424 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI SUN, SHA · 2021 to 2025
$1.6M
NCI NIH HHS R01 CA244360NCI NIH HHS R01CA244360NIGMS NIH HHS R01 GM141424NIGMS NIH HHS R01GM141424
6 · The paper itself

Abstract

The prevalence and progression of cancer differ in males and females, and thus, sexual dimorphism in tumor development directly impacts clinical research and medicine. Long non-coding RNAs (lncRNAs) are increasingly recognized as important players in gene expression and various cellular processes, including cancer development and progression. In recent years, lncRNAs have been implicated in the differences observed in cancer incidence, progression, and treatment responses between men and women. Here, we present a brief overview of the current knowledge regarding the role of lncRNAs in cancer sex dimorphism, focusing on how they affect epigenetic processes in male and female mammalian cells. We discuss the potential mechanisms by which lncRNAs may contribute to sex differences in cancer, including transcriptional control of sex chromosomes, hormonal signaling pathways, and immune responses. We also propose strategies for studying lncRNA functions in cancer sex dimorphism. Furthermore, we emphasize the importance of considering sex as a biological variable in cancer research and the need to investigate the role lncRNAs play in mediating these sex differences. In summary, we highlight the emerging link between lncRNAs and cancer sex dimorphism and their potential as therapeutic targets.

Indexed as

NeoplasmsRNA, Long NoncodingSex CharacteristicsAnimalsEpigenesis, GeneticFemaleGene Expression Regulation, NeoplasticHumansMaleSex ChromosomesRNA, Long Noncoding

Identifiers

PMID38095719
PMCPMC11176266
OpenAlexW4389742795

What OpenQuestion holds

Textmetadata
LicenceTDM
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.