Evidence map›Paper›PMID 41301413›Full record

ArticleBiomolecules2025

Long Non-Coding RNAs Contribute to Glucose Starvation-Induced Dedifferentiation in Lung Adenocarcinoma.

Aparamita Pandey, Pasquale Saggese, Adriana Soto, Estefany Gomez, Martín Alcaraz, Claudio Scafoglio

Abstract read
In one paragraph

Article in Biomolecules, 2025. 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

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

6 authors.

Aparamita PandeyDivision of Pulmonary Medicine, David Geffen School of Medicine and Jonsson Comprehensive Cancer Center, University of California Los Angeles, Los Angeles, CA 90095, USA.
Pasquale SaggeseDivision of Pulmonary Medicine, David Geffen School of Medicine and Jonsson Comprehensive Cancer Center, University of California Los Angeles, Los Angeles, CA 90095, USA.
Adriana SotoDivision of Pulmonary Medicine, David Geffen School of Medicine and Jonsson Comprehensive Cancer Center, University of California Los Angeles, Los Angeles, CA 90095, USA.
Estefany GomezDivision of Pulmonary Medicine, David Geffen School of Medicine and Jonsson Comprehensive Cancer Center, University of California Los Angeles, Los Angeles, CA 90095, USA.
Martín AlcarazDivision of Pulmonary Medicine, David Geffen School of Medicine and Jonsson Comprehensive Cancer Center, University of California Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0002-8750-752X
Claudio ScafoglioDivision of Pulmonary Medicine, David Geffen School of Medicine and Jonsson Comprehensive Cancer Center, University of California Los Angeles, Los Angeles, CA 90095, USA.

Funding

UCLA Tumor Immunology Training ProgramT32CA009120 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Steven M. Dubinett, MICHAEL A TEITELL · 1985 to 2026
$10.3M
Investigating the heterogeneity of glucose transport in lung adenocarcinomaR01CA237401 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SCAFOGLIO, CLAUDIO · 2020 to 2025
$3.1M
American Cancer Society 130696-RSG-17-003-01-CCEItalian American Cancer Foundation Fellowship (Saggese)NCI NIH HHS R01 CA237401NCI NIH HHS R01CA237401-01A1NCI NIH HHS #T32 CA009120NCI NIH HHS T32 CA009120
6 · The paper itself

Abstract

Nutrient deprivation causes dedifferentiation in solid tumors, driving an aggressive phenotype. We previously showed that glucose starvation-induced dedifferentiation is driven by epigenetic changes induced by a deficit of alpha-ketoglutarate (α-KG). Deficient activity of α-KG-dependent histone demethylases leads to unbalanced hypermethylation of histone 3 on lysine 27 (H3K27) by methyltransferase EZH2. H3K27 hypermethylation is a key mechanism of starvation-induced dedifferentiation. Here, we investigate a new aspect of this mechanism and show that epitranscriptomic changes are also induced by glucose restriction. Specifically, hypermethylation of select long non-coding RNAs leads to their upregulation under glucose deprivation as a consequence of reduced activity of the RNA demethylase FTO. We identified LINC00662 as an lncRNA required for EZH2 recruitment to target gene promoters induced by low glucose. These findings characterize the epigenetic response to glucose restriction beyond histone methylation, revealing that RNA methylation of lncRNAs such as LINC00662 represents a parallel mechanism converging on EZH2.

Indexed as

Adenocarcinoma of LungCell DedifferentiationGlucoseLung NeoplasmsRNA, Long NoncodingAlpha-Ketoglutarate-Dependent Dioxygenase FTOCell Line, TumorDNA MethylationEnhancer of Zeste Homolog 2 ProteinEpigenesis, GeneticGene Expression Regulation, NeoplasticHistonesHumansMethylationAlpha-Ketoglutarate-Dependent Dioxygenase FTOEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanFTO protein, humanGlucoseHistonesRNA, Long NoncodingdedifferentiationepitranscriptomicsEZH2FTOglucose starvationlong noncoding RNAlung adenocarcinoma

Identifiers

PMID41301413
PMCPMC12650432

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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.