Evidence map›Paper›PMID 39769395›Full record

ArticleInternational journal of molecular sciences2024

Nucleus Accumbens Associated Protein 1 in Cancers-The Real Value.

Marlena Janiczek-Polewska, Tomasz Kolenda, Paulina Poter, Inga Jagiełło, Joanna Kozłowska-Masłoń, Katarzyna Regulska, Julian Malicki, Andrzej Marszałek

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Marlena Janiczek-PolewskaDepartment of Clinical Oncology, Greater Poland Cancer Center, 61-866 Poznan, Poland.ORCID 0000-0002-1238-5273
Tomasz KolendaResearch and Implementation Unit, Greater Poland Cancer Centre, 61-866 Poznan, Poland.
Paulina PoterDepartment of Clinical Pathology, Poznan University of Medical Sciences, Greater Poland Cancer Center, 61-866 Poznan, Poland.
Inga JagiełłoDepartment of Clinical Pathology, Poznan University of Medical Sciences, Greater Poland Cancer Center, 61-866 Poznan, Poland.
Joanna Kozłowska-MasłońLaboratory of Cancer Genetics, Greater Poland Cancer Centre, 61-866 Poznan, Poland.ORCID 0000-0001-6914-4852
Katarzyna RegulskaResearch and Implementation Unit, Greater Poland Cancer Centre, 61-866 Poznan, Poland.ORCID 0000-0002-9584-3128
Julian MalickiDepartment of Electroradiology, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0002-5558-5558
Andrzej MarszałekLaboratory of Cancer Genetics, Greater Poland Cancer Centre, 61-866 Poznan, Poland.ORCID 0000-0002-6055-9151

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant tumors are a leading cause of death worldwide, second only to cardiovascular disease. They occur in every population and have a high risk of mortality. The etiopathogenesis of malignant tumors is diverse and there are still many unknowns, leading to huge diagnostic and therapeutic challenges. Therefore, the search for ideal diagnostic and therapeutic agents is ongoing. One of the promising factors affecting cancer is the nucleus accumbens associated protein 1 (NACC1). It is a transcriptional coregulator. Moreover, it plays a multifaceted role in promoting tumorigenesis. NACC1 expression analyses were performed using The Cancer Genome Atlas (TCGA) data accessed from the University of Alabama at Birmingham Cancer (UALCAN) database, and the expression data were interconnected with clinicopathological parameters. All statistical analyses were conducted using GraphPad Prism and Statistica. The results revealed that NACC1 was expressed in almost all of the analyzed cancers, and its expression level correlates with different clinicopathological parameters. This study demonstrates that NACC1 is potentially involved in the pathogenesis, invasion, and immune response associated with many cancers. However, NACC1 is not a suitable candidate as a diagnostic biomarker as it is not specific for any type of malignancy and there are discrepancies in its expression in relation to many clinicopathological parameters. The implementation of NACC1 as a therapeutic target may improve the effectiveness of cancer treatments.

Indexed as

Biomarkers, TumorNeoplasmsFemaleGene Expression Regulation, NeoplasticHumansMaleRepressor ProteinsBiomarkers, TumorRepressor ProteinscancersdiagnosticgeneticsNACC1TCGAtreatment

Identifiers

PMID39769395
PMCPMC11728236

What Socratic holds

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LicenceCC BY
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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 Socratic graph.