Evidence map›Paper›PMID 35092392›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2022

Molecular Detection of Genetic Susceptibility to Bladder Cancer in Egyptian Patients.

Samah Mamdouh, Fatma Khorshed, Gehan Hammad, Khaled Elesaily, Gehan Safwat, Olfat Hammam, Tarek Aboushousha

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
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

7 authors at 1 institution in 1 country.

Samah MamdouhDepartment of Biochemistry, Theodor Bilharz Research Institute, Cairo, Egypt.
Fatma KhorshedDepartment of Biochemistry, Theodor Bilharz Research Institute, Cairo, Egypt.
Gehan HammadFaculty of Biotechnology, MSA University, Cairo, Egypt.
Khaled ElesailyDepartment of Urology, Theodor Bilharz Research Institute, Cairo, Egypt.
Gehan SafwatFaculty of Biotechnology, MSA University, Cairo, Egypt.
Olfat HammamDepartment of Pathology, Theodor Bilharz Research Institute, Cairo, Egypt.
Tarek AboushoushaDepartment of Pathology, Theodor Bilharz Research Institute, Cairo, Egypt.
Theodor Bilharz Research Institute · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGenome-wide association studies (GWAS) have identified a number of genetic variants associated with the susceptibility of bladder cancer (BC) in European and Chinese populations. Here, we assessed the association of two of these variants, rs9642880 and rs710521 in an Egyptian patients and also examined the expression of c-Myc.The basis was due to the absence of studies on Egyptian patients to determine the association between rs9642880& rs710521 and bladder cancer risk, particularly due to the known role of the variant (rs9642880) in the Progression and development of bladder cancer.

methodsUrine samples were collected from onehundred and fiftybladder cancer patients under particular standards and fifty healthy controls. Genomic DNA was extracted,  rs9642880 G>T and rs710521 A>G polymorphisms were amplified, assessed via restriction fragment length polymorphism(RFLP) and sequenced. Urine retrieved results were compared to the histopathological diagnosis of tissue biopsies and to the results of C-Myc immunohistochemistry. Data were statistically analyzed using Microsoft Excel 2016, association between significant genotypes of the two studied variables and bladder cancer risk was performed.

resultsWe found that the TT genotype of rs9642880 G>T was strongly associated with the risk of bladder cancer, andfor rs710521 A>G, AG genotype was also identified to has an association with bladder cancer risk.All 150 tumor sections showed positive immunoreactivity for c-Myc in the nucleus and the cytoplasm.

conclusionIdentifying the association to risk of bladder cancer using genetic analysis will help in the early detection of the disease.

Indexed as

AdultBiomarkers, TumorCase-Control StudiesEgyptFemaleGenetic MarkersGenetic Predisposition to DiseaseGenetic TestingGenotypeHumansMaleMiddle AgedPolymorphism, Restriction Fragment LengthProto-Oncogene Proteins c-mycRisk AssessmentUrinary Bladder NeoplasmsBiomarkers, TumorGenetic MarkersProto-Oncogene Proteins c-mycbladder cancerc-Mycgenome-wide association studyGenotypeRFLP

Identifiers

PMID35092392
PMCPMC9258647
OpenAlexW4210710945

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.