Evidence map›Paper›PMID 31450905›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2019

Genetic Variants Related to Cell Cycle and Stability of Telomere in Patients with Glioma.

Maria Clara Jessica Calastri, Gabriela Hattori, Nicolas Luz Toledo Ortega Rodrigues, Michele Lima Gregorio, Camila Ive Ferreira Oliveira Brancati, Eliane Milharcix Zanovelo, José Roberto Lopes Ferraz Filho, Cassiano Merussi Neiva, Antonio Carlos Ponde Rodrigues Junior, Moacir Fernandes de Godoy and 3 more

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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 1 institution in 1 country.

Maria Clara Jessica CalastriDepartment of Biochemistry and Molecular Biology, Faculty of Medicine , São José do Rio Preto, São Paulo, Brazil. Email:mariaclarajessica@hotmail.comORCID 0000-0003-4413-8207
Gabriela HattoriDepartment of Biochemistry and Molecular Biology, Faculty of Medicine , São José do Rio Preto, São Paulo, Brazil. Email:mariaclarajessica@hotmail.com
Nicolas Luz Toledo Ortega RodriguesDepartament Molecular Biology on the Sao Paulo State University-"Júlio de Mesquita Filho" Campus- UNESP/IBILCE, Brazil.
Michele Lima GregorioDepartment of Biochemistry and Molecular Biology, Faculty of Medicine , São José do Rio Preto, São Paulo, Brazil. Email:mariaclarajessica@hotmail.com
Camila Ive Ferreira Oliveira BrancatiDepartment of Biochemistry and Molecular Biology, Faculty of Medicine , São José do Rio Preto, São Paulo, Brazil. Email:mariaclarajessica@hotmail.com
Eliane Milharcix ZanoveloDepartament of Patology of the Hospital de Base University Hospital of the Medical School of São José do Rio Preto - HB/FAMERP, Brazil.
José Roberto Lopes Ferraz FilhoDepartament of Patology of the Hospital de Base University Hospital of the Medical School of São José do Rio Preto - HB/FAMERP, Brazil.
Cassiano Merussi NeivaDepartment of Physical Education of the Sao Paulo State University- "Júlio de Mesquita Filho" Campus- UNESP/Campos de Bauru, Brazil.
Antonio Carlos Ponde Rodrigues JuniorDepartament of Patology of the Hospital de Base University Hospital of the Medical School of São José do Rio Preto - HB/FAMERP, Brazil.
Moacir Fernandes de GodoyDepartment of Biochemistry and Molecular Biology, Faculty of Medicine , São José do Rio Preto, São Paulo, Brazil. Email:mariaclarajessica@hotmail.com
Carmen Lucia Penteado LancellottiDepartment of Neurology of Santa Casa of São Paulo Medical Science College, Brazil.
Waldir Antonio TognolaDepartament of Neurology of the Medical School of São José do Rio Preto - FAMERP, Brazil.
Dorotéia Rossi Silva SouzaDepartment of Biochemistry and Molecular Biology, Faculty of Medicine , São José do Rio Preto, São Paulo, Brazil. Email:mariaclarajessica@hotmail.com
Faculdade de Medicina de São José do Rio Preto · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glioma, most common primary malignant brain tumor in adults, is highly aggressive and associated with a poor prognosis. Evaluate the association of polymorphisms related of to the cell cycle, integrity and DNA repair with gliomas, as well as lifestyle habits, comorbidities, survival and response to treatment. Methods: Were studied 303 individuals distributed into: Study Group - 100 patients with gliomas, regardless of the degree of malignancy, and Control Group - 203 individuals without clinical signs of the disease. These polymorphisms were genotyped by TaqMan® SNP Genotyping Assay. Significance level was set at 5%. Results: Smoking, alcohol consumption, systemic arterial hypertension (SAH) and diabetes mellitus (DM) prevailed in patients, compared to controls (P=0.0088, P=0.0001, P=0.0001, P=0.0011, respectively). In the logistic regression analysis, alcohol consumption and SAH were identified as independent risk factors for gliomas (P=0.0001, P=0.0027, respectively). Patients with low-grade gliomas showed survival in one year (92.0±6.8%), compared to patients with high-grade gliomas (24.0±5.3; P=0.011). Conclusion: Polymorphisms involved in cell cycle, telomere protection and stability and DNA repair are not associated with gliomas. On the other hand, alcohol consumption and SAH stand out as independent risk factors for the disease. Low-grade gliomas, response to treatment and the combination of chemotherapy with Temozolomide and radiation therapy show increased survival of patients.

Indexed as

Polymorphism, GeneticAdolescentAdultAgedAged, 80 and overBiomarkers, TumorBrain NeoplasmsCase-Control StudiesChildChild, PreschoolCyclin D1DNA HelicasesFemaleFollow-Up StudiesGene Expression Regulation, NeoplasticGenotypeBiomarkers, TumorCCND1 protein, humanCyclin D1DNA HelicasesRTEL1 protein, humanX-ray Repair Cross Complementing Protein 1XRCC1 protein, humanastrocytomaGlioblastomamagnetic resonance spectroscopyPolymorphism

Identifiers

PMID31450905
PMCPMC6852820
OpenAlexW2969873935

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.