Evidence map›Paper›PMID 28667494›Full record

ArticlePathology oncology research : POR2018

Single-Nucleotide Polymorphisms of the MSH2 and MLH1 Genes, Potential Molecular Markers for Susceptibility to the Development of Basal Cell Carcinoma in the Brazilian Population.

Poliane da Silva Calixto, Otávio Sérgio Lopes, Mayara Dos Santos Maia, Sylvia Satomi Takeno Herrero, Carlos Alberto Longui, Cynthia Germoglio Farias Melo, Ivan Rodrigues de Carvalho Filho, Leonardo Ferreira Soares, Arnaldo Correia de Medeiros, Plínio Delatorre and 3 more

Abstract read
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In one paragraph

Article in Pathology oncology research : POR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. The role of DNA mismatch repair in immunotherapy of human cancer.International journal of biological sciences · 2022
    Review
  3. Article
  4. Article
  5. 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

13 authors at 5 institutions in 1 country.

Poliane da Silva CalixtoLaboratório de Biologia Molecular Estrutural e Oncogenética - LBMEO, Universidade Federal da Paraíba, João Pessoa, PB, Brazil.
Otávio Sérgio LopesDepartamento de Dermatologia, Clinica Dermatológica Santa Catarina, João Pessoa, PB, Brazil.
Mayara Dos Santos MaiaLaboratório de Biologia Molecular Estrutural e Oncogenética - LBMEO, Universidade Federal da Paraíba, João Pessoa, PB, Brazil.
Sylvia Satomi Takeno HerreroLaboratório de Biologia Molecular Estrutural e Oncogenética - LBMEO, Universidade Federal da Paraíba, João Pessoa, PB, Brazil.
Carlos Alberto LonguiPrograma de Pós-Graduação em Ciências da Saúde, Faculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo SP, Brazil.
Cynthia Germoglio Farias MeloLaboratório de Biologia Molecular Estrutural e Oncogenética - LBMEO, Universidade Federal da Paraíba, João Pessoa, PB, Brazil.
Ivan Rodrigues de Carvalho FilhoDepatamento de Patologia, Laboratório de Análises Médicas - UNILAB, João Pessoa, PB, Brazil.
Leonardo Ferreira SoaresDepartamento de Farmácia, Universidade Estadual da Paraíba, Campina Grande, PB, Brazil.
Arnaldo Correia de MedeirosDepartamento de Medicina, Universidade Federal da Paraíba, João Pessoa, PB, Brazil.
Plínio DelatorreLaboratório de Biologia Molecular Estrutural e Oncogenética - LBMEO, Universidade Federal da Paraíba, João Pessoa, PB, Brazil.
André Salim KhayatInstituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.
Rommel Rodriguez BurbanoInstituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.
Eleonidas Moura LimaLaboratório de Biologia Molecular Estrutural e Oncogenética - LBMEO, Universidade Federal da Paraíba, João Pessoa, PB, Brazil. eleonidas@pq.cnpq.br.
Universidade Federal da Paraíba · BRFaculdade de Ciências Médicas da Santa Casa de São Paulo · BRUniversidade Federal do Pará · BRUniversidade Estadual da Paraíba · BRUniversity for International Integration of the Afro-Brazilian Lusophony · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Basal cell carcinoma - BCC is considered a multifactorial neoplasm involving genetic, epigenetic and environmental factors. Where UVB radiation is considered the main physical agent involved in BCC carcinogenesis. The Brazil and state of Paraíba are exposed to high levels of UVB rays. The mismatch repair - MMR is important DNA repair mechanisms to maintain replication fidelity. Therefore, single nucleotide polymorphisms (SNPs) in genes encoding proteins involved in MMR may be potential molecular markers of susceptibility to BCC. The objective of this study was to evaluate and describe for the first time the SNPs rs560246973, rs2303425 and rs565410865 and risk of developing BCC. The present study analyzed 100 samples of paraffin-embedded tissue from patients with histopathological diagnosis of BCC and 100 control samples. The results were obtained by genotyping method, Dideoxy Unique Allele Specific - PCR (DSASP). The SNPs rs2303425 were not associated with Basal Cell Carcinoma. However, the SNPs rs560246973 and rs565410865 was shown to be associated with the development of BCC when compared to control samples (P < 0.0001). The SNPs rs565410865 was also statistical significance between the genotypes of and the age group (p = 0.0027) and tumor location (p = 0,0191). The result suggests that SNPs rs2303425 and rs565410865 are associated with susceptibility to the development of BCC in the Brazilian population and may be considered as potential molecular markers for BCC.

Indexed as

Polymorphism, Single NucleotideBasal Cell CarcinomaBiomarkers, TumorBrazilCase-Control StudiesGenetic Predisposition to DiseaseHumansMutL Protein Homolog 1MutS Homolog 2 ProteinPrognosisRetrospective StudiesSkin NeoplasmsBiomarkers, TumorMLH1 protein, humanMSH2 protein, humanMutL Protein Homolog 1MutS Homolog 2 ProteinBasal cell carcinomaDSASPGenotypingMismatch repairMolecular markersSingle nucleotide polymorphism

Identifiers

PMID28667494
OpenAlexW2724934898

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.