Genetic Variants Related to Cell Cycle and Stability of Telomere in Patients with Glioma.
Maria Clara Jessica CalastriGabriela HattoriNicolas Luz Toledo Ortega RodriguesMichele Lima GregorioCamila Ive Ferreira Oliveira BrancatiEliane Milharcix ZanoveloJosé Roberto Lopes Ferraz FilhoCassiano Merussi NeivaAntonio Carlos Ponde Rodrigues JuniorMoacir Fernandes de GodoyCarmen Lucia Penteado LancellottiWaldir Antonio TognolaDorotéia Rossi Silva SouzaPublished in: Asian Pacific journal of cancer prevention : APJCP (2019)
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.
Keyphrases
- high grade
- low grade
- cell cycle
- alcohol consumption
- dna repair
- cell proliferation
- poor prognosis
- end stage renal disease
- radiation therapy
- newly diagnosed
- dna damage
- chronic kidney disease
- high throughput
- long non coding rna
- cardiovascular disease
- peritoneal dialysis
- genome wide
- arterial hypertension
- dna damage response
- gene expression
- physical activity
- weight loss
- squamous cell carcinoma
- insulin resistance
- skeletal muscle
- locally advanced
- adipose tissue
- oxidative stress
- combination therapy
- radiation induced
- neural network