Evidence map›Paper›PMID 29503660›Full record

ArticleFrontiers in genetics2017

Correlations between Risk Factors for Breast Cancer and Genetic Instability in Cancer Patients-A Clinical Perspective Study.

Márcia Fernanda Correia Jardim Paz, Marcus Vinícius Oliveira Barros de Alencar, Antonio Luiz Gomes Junior, Keylla da Conceição Machado, Muhammad Torequl Islam, Eunus S Ali, Manik Chandra Shill, Md Iqbal Ahmed, Shaikh Jamal Uddin, Ana Maria Oliveira Ferreira da Mata and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

20 authors at 6 institutions in 4 countries.

Márcia Fernanda Correia Jardim PazPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
Marcus Vinícius Oliveira Barros de AlencarPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
Antonio Luiz Gomes JuniorPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
Keylla da Conceição MachadoPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
Muhammad Torequl IslamPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
Eunus S AliSchool of Medicine, Flinders University, Adelaide, SA, Australia.
Manik Chandra ShillDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Md Iqbal AhmedPharmacy Discipline, Life Science School, Khulna University, Khulna, Bangladesh.
Shaikh Jamal UddinPharmacy Discipline, Life Science School, Khulna University, Khulna, Bangladesh.
Ana Maria Oliveira Ferreira da MataPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
Ricardo Melo de CarvalhoPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
Kátia da Conceição MachadoPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
André Luiz Pinho SobralUniversity Hospital, Federal University of Piauí, Teresina, Brazil.
Felipe Cavalcanti Carneiro da SilvaDepartment of Biological Sciences, Federal University of Piauí, Picos, Brazil.
João Marcelo de Castro E SouzaDepartment of Biological Sciences, Federal University of Piauí, Picos, Brazil.
Daniel Dias Rufino ArcanjoDepartment of Biophysics and Physiology, Universidade Federal do Piauí, Teresina, Brazil.
Paulo Michel Pinheiro FerreiraPostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
Siddhartha Kumar MishraCancer Biology Laboratory, School of Biological Sciences (Zoology), Dr. Harisingh Gour Central University, Sagar, India.
Juliana da SilvaProgram in Cellular and Molecular Biology Applied to Health Sciences, Universidade Luterana do Brasil, Canoas, Brazil.
Ana Amélia de Carvalho Melo-CavalcantePostgraduate Program in Pharmaceutical Sciences, Federal University of Piauí, Teresina, Brazil.
Universidade Federal do Piauí · BRKhulna University · BDDr. Hari Singh Gour University · INFlinders University · AUNorth South University · BDUniversidade Luterana do Brasil · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular epidemiological studies have identified several risk factors linking to the genes and external factors in the pathogenesis of breast cancer. In this sense, genetic instability caused by DNA damage and DNA repair inefficiencies are important molecular events for the diagnosis and prognosis of therapies. Therefore, the objective of this study was to analyze correlation between sociocultural, occupational, and lifestyle risk factors with levels of genetic instability in non-neoplastic cells of breast cancer patients. Total 150 individuals were included in the study that included 50 breast cancer patients submitted to chemotherapy (QT), 50 breast cancer patients submitted to radiotherapy (RT), and 50 healthy women without any cancer. Cytogenetic biomarkers for apoptosis and DNA damage were evaluated in samples of buccal epithelial and peripheral blood cells through micronuclei and comet assay tests. Elder age patients (61-80 years) had higher levels of apoptosis (catriolysis by karyolysis) and DNA damage at the diagnosis (baseline damage) with increased cell damage during QT and especially during RT. We also reported the increased frequencies of cytogenetic biomarkers in patients who were exposed to ionizing radiation as well as for alcoholism and smoking. QT and RT induced high levels of fragmentation (karyorrhexis) and nuclear dissolution (karyolysis) and DNA damage. Correlations were observed between age and karyorrhexis at diagnosis; smoking and karyolysis during RT; and radiation and karyolysis during QT. These correlations indicate that risk factors may also influence the genetic instability in non-neoplastic cells caused to the patients during cancer therapies.

Indexed as

apoptosisbreast cancerchemotherapygenetic instabilityrisk factorstoxicogenomics

Identifiers

PMID29503660
PMCPMC5821102
OpenAlexW2787340663

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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.