Evidence map›Paper›PMID 39488528›Full record

ArticleCell death & disease2024

G9a/DNMT1 co-targeting inhibits non-small cell lung cancer growth and reprograms tumor cells to respond to cancer-drugs through SCARA5 and AOX1.

Francisco Exposito, Miriam Redrado, Diego Serrano, Silvia Calabuig-Fariñas, Aida Bao-Caamano, Sandra Gallach, Eloisa Jantus-Lewintre, Angel Diaz-Lagares, Aitor Rodriguez-Casanova, Juan Sandoval and 13 more

Abstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

23 authors.

Francisco ExpositoProgram in Solid Tumors, Cima-Universidad de Navarra, Cancer Center Clinica Universidad de Navarra (CCUN), Pamplona, Spain.ORCID 0000-0002-5406-0768
Miriam RedradoProgram in Solid Tumors, Cima-Universidad de Navarra, Cancer Center Clinica Universidad de Navarra (CCUN), Pamplona, Spain.
Diego SerranoProgram in Solid Tumors, Cima-Universidad de Navarra, Cancer Center Clinica Universidad de Navarra (CCUN), Pamplona, Spain.
Silvia Calabuig-FariñasCIBERONC, ISCIII, Madrid, Spain.
Aida Bao-CaamanoEpigenomics Units, Cancer Epigenomics, Translational Medical Oncology Group (ONCOGAL), Health Research Institute of Santiago de Compostela (IDIS), and Department of Clinical Analysis, University Hospital Complex of Santiago de Compostela (CHUS), Roche-CHUS Joint Unit (ONCOMET), Health Research Institute of Santiago (IDIS), 15706, Santiago de Compostela, Spain, 15706, Santiago de Compostela, Spain.
Sandra GallachCIBERONC, ISCIII, Madrid, Spain.
Eloisa Jantus-LewintreCIBERONC, ISCIII, Madrid, Spain.ORCID 0000-0001-7395-4380
Angel Diaz-LagaresCIBERONC, ISCIII, Madrid, Spain.
Aitor Rodriguez-CasanovaEpigenomics Units, Cancer Epigenomics, Translational Medical Oncology Group (ONCOGAL), Health Research Institute of Santiago de Compostela (IDIS), and Department of Clinical Analysis, University Hospital Complex of Santiago de Compostela (CHUS), Roche-CHUS Joint Unit (ONCOMET), Health Research Institute of Santiago (IDIS), 15706, Santiago de Compostela, Spain, 15706, Santiago de Compostela, Spain.
Juan SandovalBiomarkers and Precision Medicine (UBMP) and Epigenomics Unit, IIS, La Fe, 46026, Valencia, Spain.
Edurne San Jose-EnerizCIBERONC, ISCIII, Madrid, Spain.
Javier GarciaDepartment of Pathology, Anatomy and Physiology, School of Medicine, University of Navarra, Pamplona, Spain.
Esther RedinProgram in Solid Tumors, Cima-Universidad de Navarra, Cancer Center Clinica Universidad de Navarra (CCUN), Pamplona, Spain.
Yaiza SenentProgram in Solid Tumors, Cima-Universidad de Navarra, Cancer Center Clinica Universidad de Navarra (CCUN), Pamplona, Spain.
Sergio LeonProgram in Solid Tumors, Cima-Universidad de Navarra, Cancer Center Clinica Universidad de Navarra (CCUN), Pamplona, Spain.
Ruben PioProgram in Solid Tumors, Cima-Universidad de Navarra, Cancer Center Clinica Universidad de Navarra (CCUN), Pamplona, Spain.ORCID 0000-0002-6831-6111
Rafael LopezCIBERONC, ISCIII, Madrid, Spain.
Julen OyarzabalMolecular Therapeutics Program, CIMA, CCUN, University of Navarra, Pamplona, Spain.
Antonio Pineda-LucenaMolecular Therapeutics Program, CIMA, CCUN, University of Navarra, Pamplona, Spain.
Xabier AgirreCIBERONC, ISCIII, Madrid, Spain.ORCID 0000-0002-6558-9560
Luis M MontuengaProgram in Solid Tumors, Cima-Universidad de Navarra, Cancer Center Clinica Universidad de Navarra (CCUN), Pamplona, Spain.
Felipe ProsperCIBERONC, ISCIII, Madrid, Spain.ORCID 0000-0001-6115-8790
Alfonso CalvoProgram in Solid Tumors, Cima-Universidad de Navarra, Cancer Center Clinica Universidad de Navarra (CCUN), Pamplona, Spain. acalvo@unav.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment of non-small cell lung cancer (NSCLC) patients has significantly improved with recent therapeutic strategies; however, many patients still do not benefit from them. As a result, new treatment approaches are urgently needed. In this study, we evaluated the antitumor efficacy of co-targeting G9a and DNMT1 enzymes and its potential as a cancer drug sensitizer. We observed co-expression and overexpression of G9a and DNMT1 in NSCLC, which were associated with poor prognosis. Co-targeting G9a/DNMT1 with the drug CM-272 reduced proliferation and induced cell death in a panel of human and murine NSCLC cell lines. Additionally, the transcriptomes of these cells were reprogrammed to become highly responsive to chemotherapy (cisplatin), targeted therapy (trametinib), and epigenetic therapy (vorinostat). In vivo, CM-272 reduced tumor volume in human and murine cell-derived cancer models, and this effect was synergistically enhanced by cisplatin. The expression of SCARA5 and AOX1 was induced by CM-272, and both proteins were found to be essential for the antiproliferative response, as gene silencing decreased cytotoxicity. Furthermore, the expression of SCARA5 and AOX1 was positively correlated with each other and inversely correlated with G9a and DNMT1 expression in NSCLC patients. SCARA5 and AOX1 DNA promoters were hypermethylated in NSCLC, and SCARA5 methylation was identified as an epigenetic biomarker in tumors and liquid biopsies from NSCLC patients. Thus, we demonstrate that co-targeting G9a/DNMT1 is a promising strategy to enhance the efficacy of cancer drugs, and SCARA5 methylation could serve as a non-invasive biomarker to monitor tumor progression.

Indexed as

Carcinoma, Non-Small-Cell LungCell ProliferationDNA (Cytosine-5-)-Methyltransferase 1Histone-Lysine N-MethyltransferaseLung NeoplasmsAnimalsAntineoplastic AgentsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHistocompatibility AntigensHumansMiceAntineoplastic AgentsDNA (Cytosine-5-)-Methyltransferase 1DNMT1 protein, humanEHMT2 protein, humanHistocompatibility AntigensHistone-Lysine N-Methyltransferase

Identifiers

PMID39488528
PMCPMC11531574

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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.