Evidence map›Paper›PMID 31031231›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2019

Survivin Promoter Polymorphism (-31 C/G): A Genetic Risk Factor for Oral Cancer

Rehana Faryal Mehdi, Fouzia Sheikh, Rizma Khan, Bina Fawad, Ahteshaam Ul Haq

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 41% 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, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. International journal of molecular sciences · 2023
    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

5 authors at 1 institution in 1 country.

Rehana Faryal MehdiDepartment of Pathology, Ziauddin University Clifton campus, Karachi, Pakistan. Email: faryalmehdi14@gmail.com
Fouzia SheikhDepartment of Pathology, Ziauddin University Clifton campus, Karachi, Pakistan. Email: faryalmehdi14@gmail.com
Rizma KhanDepartment of Molecular Genetic, Ziauddin University North Nazimabad campus, Karachi, Pakistan.
Bina FawadDepartment of Community medicine, Ziauddin University Clifton campus, Karachi, Pakistan.
Ahteshaam Ul HaqDepartment of Molecular Genetic, Ziauddin University North Nazimabad campus, Karachi, Pakistan.
Ziauddin University · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The polymorphism of survivin gene at its promoter region is one of the risk factors for OSCC . This polymorphism involves substitution of G for C (9904341), and it is present at the cell cycle dependent elements and cell cycle homology region repressor binding motif of promoter. This study aimed to find the association between survivin -31C/G polymorphism and prevalence of OSCC in a subset of Pakistani population. Methodology: This case-control study was conducted on 47 cases with and 101 healthy individuals with no family history of cancer. We used polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) protocols. Results: The most common site of oral cancer in our research was the buccal mucosa followed by tongue and the least one was the labial mucosa. The histological tumor type of all 47 cases was squamous cell type. In our research, stage II had the highest prevalence, accounting for 34% of patients, while the prevalence of stage I was 31% in the case group. The prevalence of stage III and IV was 25% and 8%, respectively. The numbers of moderately and poorly differentiated tumors were equal. We found a significant association between the CC genotype of survivin and OSCC prevalence (OR was 9.395 at 95% CI: 1.0202-86.5251, p-value= 0.04). The GG genotype also showed significant P value (OR: 0.4709 with 95% CI: 0.2323- 0.9546 at a P VALUE of 0.0367). while no significant P value was noted for CG genotype (OR: 1.4317 with 95% CI: 0.7513 -2.8658, p- value= 0.31). Conclusion: Survivin -31G/C polymorphism was strongly associated with OSCC prevalence. The C allele was more common in case group as compared to healthy individuals living in Pakistan.

Indexed as

Polymorphism, Single NucleotidePromoter Regions, GeneticAdultBiomarkers, TumorCarcinoma, Squamous CellCase-Control StudiesFemaleFollow-Up StudiesHumansIncidenceMaleMiddle AgedMouth NeoplasmsPakistanPrognosisRisk FactorsBiomarkers, TumorBIRC5 protein, humanSurvivin31G/C polymorphismOral squamous cell carcinomaSurvivin

Identifiers

PMID31031231
PMCPMC6948886
OpenAlexW2942287794

What OpenQuestion 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 OpenQuestion graph.