Evidence map›Paper›PMID 36974538›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2023

VNTR Polymorphism in the Intron 5 of SIRT3 and Susceptibility to Breast Cancer.

Harshitha Yadav Payavula, Deepika Jamadandu, Salomy Velpula, Raghunadha Rao Digumarti, Vishnupriya Satti, Sandhya Annamaneni

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2023. 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
0.5field-weighted citation impact, top 37% 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, 3 citations in OpenAlex.

  1. Sirtuins in Women's Health.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  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

6 authors at 1 institution in 1 country.

Harshitha Yadav PayavulaDepartment of Genetics and Biotechnology, University College of Science, Osmania University, Hyderabad, India.
Deepika JamadanduDepartment of Genetics and Biotechnology, University College of Science, Osmania University, Hyderabad, India.
Salomy VelpulaDepartment of Genetics and Biotechnology, University College of Science, Osmania University, Hyderabad, India.
Raghunadha Rao DigumartiNizams Institute of Medical Sciences (NIMS), Hyderabad, Telangana, India.
Vishnupriya SattiGenome Foundation, Hyderabad, Telangana, India.
Sandhya AnnamaneniDepartment of Genetics and Biotechnology, University College of Science, Osmania University, Hyderabad, India.
Osmania University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer recurrence and metastasis are associated with alterations in the cellular stress responses that influence tumour signalling. Sirtuin3 (SIRT3), a mitochondrial deacetylase is the regulator of mitochondrial metabolism and oxidative stress affecting tumour cell responses. Genetic variants or dysregulation of SIRT3 was known to associate with poor prognosis of recurrence and relapse in few cancers.

methodsThe current case-control study was conducted in Hyderabad, India. A total of 200 primary female breast cancer cases were recruited, irrespective of age and clinical subtype. However, secondary or recurrent breast cancer cases were excluded from the study. A total of 202 age and gender-matched healthy controls without any familial inheritance of either breast or other cancer and having similar ethnicity as cases were recruited. The blood samples of both cases and controls were collected from Nizam's Institute of Medical Sciences (NIMS), Hyderabad. Our study is an attempt to evaluate the association of SIRT3 VNTR polymorphism in intron 5 with the development and progression of breast cancer by PCR-based genotyping.  Result: The statistical analysis of the results with respect to epidemiological and clinical phenotypes revealed significant association of 0R allele and 0R/0R genotype with breast cancer risk (p<0.01). The odds ratios also were found to be significant i.e., 0R/0R [OR(CI): 2.67(1.54-4.65); p=0.000005] genotype. Also, the epidemiological and clinical variables have shown significant association with the risk of onset of the disease. Therefore, the influence of lack of repeats at intron 5 harbouring enhancer site on altered expression of SIRT3 might confer increased susceptibility to breast cancer.

conclusionThe VNTR polymorphism in the intron 5 region of SIRT3 gene could serve as a molecular marker for detection of breast cancer onset. Further studies are warranted to study the prognostic and therapeutic significance of this SIRT3 polymorphism.

Indexed as

Breast NeoplasmsSirtuin 3Case-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansIntronsMinisatellite RepeatsNeoplasm Recurrence, LocalPolymorphism, GeneticSIRT3 protein, humanSirtuin 3associationMitochondrial metabolismPrognosisRelapseTumour signalling

Identifiers

PMID36974538
PMCPMC10334083
OpenAlexW4361214861

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.