Evidence map›Paper›PMID 36534235›Full record

ArticleMolecular biology reports2023

Association of CCND1 (c.723G > A, rs9344) variant with elevated risk of breast carcinoma: a retrospective case-control study.

Mohamed Adel El-Eshmawy, Hanaa Elsayed Shahin, Nanis S El-Beltagy, Dina Abdel Hamid, Ola M Elfarargy, Dalia Hamouda Elsayed, Afaf M Elsaid, Rami M Elshazli, Noura M Mohamed

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

9 authors at 6 institutions in 2 countries.

Mohamed Adel El-EshmawyClinical Pathology Department, Mansoura University Hospital, Mansoura University, Mansoura, Egypt.
Hanaa Elsayed ShahinNursing Department, College of Applied Medial Sciences, Jouf University, ElQurayyat, Saudi Arabia.
Nanis S El-BeltagyFaculty of Medicine, Children's University Hospital, Mansoura University, Mansoura, Egypt.
Dina Abdel HamidHematology and Bone Marrow Transplant Unit, Children's University Hospital, Mansoura University, Mansoura, Egypt.
Ola M ElfarargyDepartment of Medical Oncology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Dalia Hamouda ElsayedDepartment of Medical Oncology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Afaf M ElsaidGenetic Unit, Children's University Hospital, Mansoura University, Mansoura, Egypt.
Rami M ElshazliBiochemistry and Molecular Genetics Unit, Department of Basic Sciences, Faculty of Physical Therapy, Horus University - Egypt, New Damietta, Egypt. Relshazly@horus.edu.eg.ORCID http://orcid.org/0000-0002-3381-2641
Noura M MohamedDepartment of Medical Biochemistry, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Children's Hospital Mansoura University · EGZagazig University · EGDamietta University · EGJouf University · SAMansoura University Hospital · EGPrincess Nourah bint Abdulrahman University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prevalence rate of breast carcinoma (BC) among multiple ethnic populations required more explanations to understand the pathogenesis mechanisms for the development of this type of cancer. The principal purpose of this work is to validate the correlation of the CCND1 (c.723G > A; rs9344) variant with an increased risk of breast carcinoma.

methodsThis retrospective case-controlled study was designed appertaining to 200 women including 100 BC patients and 100 unrelated cancer-free controls. The amplification of genomic DNA was genotyped utilizing the PCR-RFLP technique.

resultsThe frequencies of the CCND1 (c.723G > A; rs9344) variant revealed a significant association with increased risk of breast carcinoma under different genetic models including allelic (OR = 2.84, P-value < 0.001), recessive (OR = 4.83, P-value < 0.001), and dominant (OR = 3.19, P-value < 0.001) models.

conclusionsOur findings concluded that the genetic biomarker of the CCND1 (c.723G > A; rs9344) variant is correlated with an elevated risk of breast carcinoma among Egyptian women.

Indexed as

Breast NeoplasmsPolymorphism, Single NucleotideCase-Control StudiesCyclin D1FemaleGenetic Predisposition to DiseaseGenotypeHumansNorth African PeopleRetrospective StudiesCCND1 protein, humanCyclin D1CCND1Genetic variant and Breast carcinomars9344

Identifiers

PMID36534235
OpenAlexW4311930107

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.