Evidence map›Paper›PMID 33146350›Full record

ArticleClinics (Sao Paulo, Brazil)2020

Association between matrix metalloproteinase-9 gene polymorphism and breast cancer in Brazilian women.

Victor Alves de Oliveira, Diego Cipriano Chagas, Jefferson Rodrigues Amorim, Renato de Oliveira Pereira, Thais Alves Nogueira, Victória Maria Luz Borges, Larysse Maira Campos-Verde, Luana Mota Martins, Gilmara Peres Rodrigues, Elmo de Jesus Nery Júnior and 6 more

Open access · goldAbstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

16 authors at 1 institution in 1 country.

Victor Alves de OliveiraPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0003-1039-7657
Diego Cipriano ChagasPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0003-2964-4144
Jefferson Rodrigues AmorimPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0002-7260-4239
Renato de Oliveira PereiraPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0003-4423-1575
Thais Alves NogueiraPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0001-7459-8189
Victória Maria Luz BorgesPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0003-3956-6864
Larysse Maira Campos-VerdePrograma de Doutorado em Biotecnologia - Rede Nordeste de Biotecnologia (RENORBIO), Universidade Federal do Piaui, PI, BR.ORCID 0000-0001-6064-149X
Luana Mota MartinsPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0002-2521-5820
Gilmara Peres RodriguesPrograma de Doutorado em Biotecnologia - Rede Nordeste de Biotecnologia (RENORBIO), Universidade Federal do Piaui, PI, BR.ORCID 0000-0003-2770-8191
Elmo de Jesus Nery JúniorPrograma de Doutorado em Biotecnologia - Rede Nordeste de Biotecnologia (RENORBIO), Universidade Federal do Piaui, PI, BR.ORCID 0000-0003-0225-5384
Fabiane Araújo SampaioPrograma de Doutorado em Biotecnologia - Rede Nordeste de Biotecnologia (RENORBIO), Universidade Federal do Piaui, PI, BR.ORCID 0000-0002-9449-5045
Pedro Vitor Lopes-CostaPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0003-2985-4352
João Marcelo de Castro E SousaPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0002-5085-1482
Vladmir Costa SilvaPrograma de Doutorado em Biotecnologia - Rede Nordeste de Biotecnologia (RENORBIO), Universidade Federal do Piaui, PI, BR.ORCID 0000-0003-3109-7899
Felipe Cavalcanti Carneiro da SilvaPrograma de Doutorado em Biotecnologia - Rede Nordeste de Biotecnologia (RENORBIO), Universidade Federal do Piaui, PI, BR.ORCID 0000-0002-4241-3036
Benedito Borges da SilvaPrograma de Pos-Graduacao em Ciencias e Saude, Universidade Federal do Piaui, PI, BR.ORCID 0000-0002-9542-7538
Universidade Federal do Piauí · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to determine the relationship between rs17576 (MMP-9) polymorphism and increased cancer risk in a Brazilian breast cancer cohort.

methodsThis study included 141 women (71 breast cancer patients and 70 controls without breast cancer) who donated 3 mL of their peripheral blood for genomic DNA extraction. This DNA was then genotyped using a real-time polymerase chain reaction.

resultsThe AG (rs17576) genotype was identified in 26 (18.43%) participants in the case group and in 22 (15.60%) participants in the control group (p=0.274), while the GG genotype was identified in ten (7.09%) participants in the case group and in one (0.70%) participant in the control group (p<0.003 - OR (95% CI) 13.13 (1.73, 593.08). No significant difference in the incidence rates was observed for AG or GG rs17576 genotypes in premenopausal women, p=0.813 and p=0.556, respectively. However, in postmenopausal women, the AG genotype was shown to occur in 14 (22.5%) participants in the case group and in 4 (6.45%) participants in the control (p<0.043), while GG genotype occurred in eight (12.90%) of the individuals in the case group and in none of the individuals in the control group (p<0.006).

conclusionIn this study, the MMP-9 rs17576 GG polymorphic variant was shown to be significantly associated with breast cancer risk in premenopausal women, while the AG and GG genotypes were associated with increased cancer risk in postmenopausal women.

Indexed as

Breast NeoplasmsMatrix Metalloproteinase 9BrazilCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansPolymorphism, Single NucleotideRisk FactorsMatrix Metalloproteinase 9MMP9 protein, human

Identifiers

PMID33146350
PMCPMC7561070
OpenAlexW3095468001

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.