Evidence map›Paper›PMID 28961241›Full record

ArticlePloS one2017

Synergistic effect of collagenase-1 (MMP1), stromelysin-1 (MMP3) and gelatinase-B (MMP9) gene polymorphisms in breast cancer.

Chiranjeevi Padala, Mohini Aiyengar Tupurani, Kaushik Puranam, Srilatha Gantala, Nivas Shyamala, Mrudula Spurthi Kondapalli, Kishore Kumar Gundapaneni, Saraswati Mudigonda, Rajesh Kumar Galimudi, Keerthi Kupsal and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 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 2 institutions in 1 country.

Chiranjeevi PadalaDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Mohini Aiyengar TupuraniDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Kaushik PuranamDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Srilatha GantalaDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Nivas ShyamalaDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Mrudula Spurthi KondapalliDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Kishore Kumar GundapaneniDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Saraswati MudigondaDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Rajesh Kumar GalimudiDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Keerthi KupsalDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Santoshi Rani NanchariDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Uday ChavanMNJ Institute of Oncology & Regional Cancer Centre, Red Hills, Hyderabad, Telangana State, India.
Sanjeeva Kumari ChintaMNJ Institute of Oncology & Regional Cancer Centre, Red Hills, Hyderabad, Telangana State, India.
Srinivasulu MuktaMNJ Institute of Oncology & Regional Cancer Centre, Red Hills, Hyderabad, Telangana State, India.
Vishnupriya SattiDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.
Surekha Rani HanumanthDepartment of Genetics, Osmania University, Hyderabad, Telangana State, India.ORCID http://orcid.org/0000-0002-7522-9569
Osmania University · INMNJ Institute Of Oncology and Regional Cancer Centre · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExtracellular matrix degradation by matrix metalloproteinases (MMPs) is an important mechanism involved in tumor invasion and metastasis. Genetic variations of MMPs have shown association with multiple cancers. The present study is focused to elucidate the association of MMP-1, 3 and 9 genetic variants with respect to epidemiological and clinicopathological variables by haplotype, LD, MDR, survival in silico analyses among South Indian women. MATERIAL AND

methodsMMP3-1171 5A/6A and MMP9-1562 C/T SNPs were genotyped by Allele specific polymerase chain reaction and MMP1-1607 1G/2G polymorphism by restriction fragment length polymorphism assays respectively, in 300 BC patients and age-matched 300 healthy controls. Statistical analysis was performed using the SNPStats and SPSS software. Linkage disequilibrium and gene-gene interactions were performed using Haploview and MDR software respectively. Further, transcription factor binding sites in the promoter regions of SNPs under study were carried out using AliBaba2.1 software.

resultsWe have observed an increased frequency of 2G-allele of MMP1, 6A-allele of MMP3 and T-allele of MMP9 (p<0.05) respectively in BC subjects. The 2G-6A haplotype (minor alleles of MMP-1 and MMP-3 respectively) has shown an increased susceptibility to BC. Further, MMP polymorphisms were associated with the clinical characteristics of BC patients such as steroid hormone receptor status, lymph node involvement and metastasis. SNP combinations were in perfect LD in controls. MDR analysis revealed a positive interaction between the SNPs. 5-years survival rate and cox-regression analysis showed a significant association with clinicopathological variables.

conclusionOur results suggest that MMP1-1607 1G/2G, MMP3-1171 5A/6A and MMP9-1562 C/T gene polymorphisms have synergistic effect on breast cancer. The interactions of MMPs clinical risk factors such as lymph node involvement has shown a strong correlation and might influence the 5-years survival rate, suggesting their potential role in the breast carcinogenesis.

Indexed as

Polymorphism, Single NucleotideAdultAllelesBreast NeoplasmsCase-Control StudiesFemaleGene FrequencyGenotypeHaplotypesHumansLinkage DisequilibriumMatrix Metalloproteinase 1Matrix Metalloproteinase 3Matrix Metalloproteinase 9Middle AgedPolymerase Chain ReactionMatrix Metalloproteinase 1Matrix Metalloproteinase 3Matrix Metalloproteinase 9MMP3 protein, human

Identifiers

PMID28961241
PMCPMC5621673
OpenAlexW2757371372

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.