Evidence map›Paper›PMID 37511924›Full record

ArticleLife (Basel, Switzerland)2023

The Reticulon-4 3-bp Deletion/Insertion Polymorphism Is Associated with Structural mRNA Changes and the Risk of Breast Cancer: A Population-Based Case-Control Study with Bioinformatics Analysis.

Pouria Pourzand, Farhad Tabasi, Fariba Fayazbakhsh, Shamim Sarhadi, Gholamreza Bahari, Mohsen Mohammadi, Sahar Jomepour, Mohammad Nafeli, Fatemeh Mosayebi, Mehrdad Heravi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2023. 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
0.2field-weighted citation impact, top 42% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

13 authors at 6 institutions in 2 countries.

Pouria PourzandDepartment of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan 9816743463, Iran.ORCID 0000-0003-2662-9491
Farhad TabasiDepartment of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan 9816743463, Iran.ORCID 0000-0003-4877-0701
Fariba FayazbakhshSchool of Medicine, Zahedan University of Medical Science, Zahedan 9816743463, Iran.
Shamim SarhadiFaculty of Advanced Medical Sciences, Department of Medical Biotechnology, Tabriz University of Medical Sciences, Tabriz 5166616471, Iran.
Gholamreza BahariDepartment of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan 9816743463, Iran.
Mohsen MohammadiSchool of Medicine, Zahedan University of Medical Science, Zahedan 9816743463, Iran.ORCID 0000-0002-3256-3209
Sahar JomepourDepartment of Cardiology, Cardiovascular Research Center, School of Medicine, Hormozgan University of Medical Science, Bandar Abbas 7916613885, Iran.
Mohammad NafeliSchool of Medicine, Zahedan University of Medical Science, Zahedan 9816743463, Iran.ORCID 0000-0002-5229-8449
Fatemeh MosayebiTehran Heart Center, Tehran University of Medical Science, Tehran 1416634793, Iran.
Mehrdad HeraviSchool of Medicine, Zahedan University of Medical Science, Zahedan 9816743463, Iran.
Mohsen TaheriGenetics of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan 9816743463, Iran.ORCID 0000-0002-1110-4417
Mohammad HashemiDepartment of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan 9816743463, Iran.ORCID 0000-0002-6074-7101
Saeid GhavamiResearch Institute of Oncology and Hematology, Cancer Care Manitoba-University of Manitoba, Winnipeg, MB R3E 0V9, Canada.ORCID 0000-0001-5948-508X
Zahedan University of Medical Sciences · IRCancerCare Manitoba · CATabriz University of Medical Sciences · IRTarbiat Modares University · IRTehran University of Medical Sciences · IRUniversity of Hormozgan · IR

Funding

Zahedan University of Medical Sciences 8921
6 · The paper itself

Abstract

Breast cancer (BC) is a complex disease caused by molecular events that disrupt cellular survival and death. Discovering novel biomarkers is still required to better understand and treat BC. The reticulon-4 (RTN4) gene, encoding Nogo proteins, plays a critical role in apoptosis and cancer development, with genetic variations affecting its function. We investigated the rs34917480 in RTN4 and its association with BC risk in an Iranian population sample. We also predicted the rs34917480 effect on RTN4 mRNA structure and explored the RTN4's protein-protein interaction network (PPIN) and related pathways. In this case-control study, 437 women (212 BC and 225 healthy) were recruited. The rs34917480 was genotyped using AS-PCR, mRNA secondary structure was predicted with RNAfold, and PPIN was constructed using the STRING database. Our findings revealed that this variant was associated with a decreased risk of BC in heterozygous (

Indexed as

breast cancerpolymorphismrs34917480RTN4

Identifiers

PMID37511924
PMCPMC10381770
OpenAlexW4384130935

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.