Evidence map›Paper›PMID 37754231›Full record

ArticleCurrent issues in molecular biology2023

Long Noncoding RNA TALAM1 Is a Transcriptional Target of the RUNX2 Transcription Factor in Lung Adenocarcinoma.

Gisella Bermúdez, Camila Bernal, Andrea Otalora, Paula Sanchez, Gino Nardocci, Alejandra Cañas, Liliana Lopez-Kleine, Martín Montecino, Adriana Rojas

Open access · goldAbstract read
In one paragraph

Article in Current issues in molecular biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Gisella BermúdezInstitute of Human Genetics, Facultad de Medicina, Pontificia Universidad Javeriana Bogotá, Bogotá 110231, Colombia.ORCID 0000-0002-6563-7067
Camila BernalInstitute of Human Genetics, Facultad de Medicina, Pontificia Universidad Javeriana Bogotá, Bogotá 110231, Colombia.
Andrea OtaloraInstitute of Human Genetics, Facultad de Medicina, Pontificia Universidad Javeriana Bogotá, Bogotá 110231, Colombia.ORCID 0000-0002-5668-0266
Paula SanchezInstitute of Human Genetics, Facultad de Medicina, Pontificia Universidad Javeriana Bogotá, Bogotá 110231, Colombia.
Gino NardocciSchool of Medicine, Faculty of Medicine, Universidad de los Andes, Santiago 7620001, Chile.ORCID 0000-0002-2342-6480
Alejandra CañasDepartamento de Medicina Interna, Facultad de Medicina, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Liliana Lopez-KleineDepartamento de Estadística, Universidad Nacional de Colombia, Bogotá 111321, Colombia.ORCID 0000-0001-9325-9529
Martín MontecinoInstitute of Biomedical Sciences, Facultad de Medicina y Facultad de Ciencias de la Vida, Universidad Andres Bello, Santiago 8370134, Chile.ORCID 0000-0002-6025-0023
Adriana RojasInstitute of Human Genetics, Facultad de Medicina, Pontificia Universidad Javeriana Bogotá, Bogotá 110231, Colombia.ORCID 0000-0001-8528-4433
Pontificia Universidad Javeriana · COUniversidad Andrés Bello · CLUniversidad de Los Andes, Chile · CLUniversidad Nacional de Colombia · CO

Funding

Pontificia Universidad Javeriana 6659
6 · The paper itself

Abstract

backgroundLung cancer is the leading cause of cancer death worldwide. It has been reported that genetic and epigenetic factors play a crucial role in the onset and evolution of lung cancer. Previous reports have shown that essential transcription factors in embryonic development contribute to this pathology. Runt-related transcription factor (RUNX) proteins belong to a family of master regulators of embryonic developmental programs. Specifically, RUNX2 is the master transcription factor (TF) of osteoblastic differentiation, and it can be involved in pathological conditions such as prostate, thyroid, and lung cancer by regulating apoptosis and mesenchymal-epithelial transition processes. In this paper, we identified

methodsWe performed ChIP-seq analysis of tumor samples from a patient diagnosed with lung adenocarcinoma to evaluate the target genes of the RUNX2 TF. In addition, we performed shRNA-mediated knockdown of RUNX2 in this lung adenocarcinoma cell line to confirm the regulatory role of RUNX2 in

resultsWe observed RUNX2 overexpression in cell lines and primary cultured lung cancer cells. Interestingly, we found that lncRNA TALAM1 was a target of RUNX2 and that RUNX2 exerted a negative regulatory effect on

Indexed as

ChIP-seqlung cancerRUNX2TALAM1

Identifiers

PMID37754231
PMCPMC10529414
OpenAlexW4386137893

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.