Ana Lívia Silva Galbiatti-Dias

Dr. Ana Lívia Silva Galbiatti-Dias

orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 November 2015 in Brazilian Journal of Otorhinolaryngology
Verified
Journal Article
Open access
AGAna Lívia Silva Galbiatti-Dias
Ana Lívia Silva Galbiatti-Dias
JPJoão Armando Padovani-Junior
João Armando Padovani-Junior
JMJosé Victor Maníglia
José Victor Maníglia
CRCléa Dometilde Soares Rodrigues
Cléa Dometilde Soares Rodrigues
ÉPÉrika Cristina Pavarino
Érika Cristina Pavarino
EGEny Maria Goloni-Bertollo
Eny Maria Goloni-Bertollo
Although head and neck carcinoma ranks fifth among cancer types, patient survival rates have not changed significantly over the past years. To determine the risk factors, causes, therapies, and prevention measures for head and neck cancer. Risk factors, causes, therapies, and preventive measures for this disease were searched on databases PUBMED, MEDLINE, and SCIELO. Alcohol and tobacco are still atop risk factors. Other factors may influence the development of head and neck carcinoma. Surgery is the main treatment option, and the addition of radiotherapy following surgery is frequent for patients in the early stages of the disease. Other therapies target specific genetic molecular components connected to tumor development. Disease preventive measures include smoking cessation, limiting alcohol intake, preventing exposure to tobacco smoke and environmental carcinogenic agents, early detection of infection by HPV, maintaining oral health, good eating habits, and managing stress. Additional research is needed for a more thorough understanding of the development of head and neck carcinomas and to shed light on new ways to improve therapeutic approaches and interventions.

1 July 2012 in European Journal of Cancer
Verified
Journal Article
Closed access
AGAna Lívia Silva Galbiatti-Dias
Ana Lívia Silva Galbiatti-Dias
LALidia Maria Rebolho Batista Arantes
Lidia Maria Rebolho Batista Arantes
MRMariangela Torreglosa Ruiz-Cintra
Mariangela Torreglosa Ruiz-Cintra
LRLuis Sérgio Raposo
Luis Sérgio Raposo
JMJosé Victor Maníglia
José Victor Maníglia
EGEny Maria Goloni-Bertollo
Eny Maria Goloni-Bertollo

1 January 2016 in Genetics and Molecular Research
Verified
Journal Article
Closed access
TZT. Zara-Lopes
T. Zara-Lopes
AGA.P.A. Gimenez-Martins
A.P.A. Gimenez-Martins
CNC.H.V. Nascimento-Filho
C.H.V. Nascimento-Filho
MCMárcia Maria U Castanhole-Nunes
Márcia Maria U Castanhole-Nunes
AGAna Lívia Silva Galbiatti-Dias
Ana Lívia Silva Galbiatti-Dias
EGE.M. Goloni-Bertollo
E.M. Goloni-Bertollo
Folate metabolism is essential for DNA synthesis and repair. Alterations in genes that participate in folate metabolism can be associated with several types of malignant neoplasms, including thyroid and breast cancer. In the present case-control study, we examined the association between methylenetetrahydrofolate reductase (MTHFR C677T, rs1801133) and methionine synthase (MTR A2756G, rs1805087) polymorphisms and risk for thyroid and breast cancer. Polymerase chain reaction-restriction fragment length technique was used to determine the specific genotypes in the genes of interest. Statistical analysis was performed by multiple logistic regression test. We found an association between MTHFR C677T polymorphism and risks to both thyroid (OR = 2.50; 95% CI = 1.15-5.46; P = 0.02) and breast cancer (OR = 2.53; 95% CI = 1.08-5.93; P = 0.03). Tobacco consumption and high body mass index were also associated with thyroid cancer. In addition, increased age (= 50 years) and alcohol consumption were found to be associated with breast cancer. Our results indicated that MTHFR C677T is significantly associated with thyroid and breast cancer risks. Thus, these factors may be used as potential prognostic markers for thyroid and breast cancers.

10 May 2011 in Molecular Biology Reports
Verified
Journal Article
Closed access
PDF file
AGAna Lívia Silva Galbiatti-Dias
Ana Lívia Silva Galbiatti-Dias
MRMariangela Torreglosa Ruiz
Mariangela Torreglosa Ruiz
JRJuliana Olsen Rodrigues
Juliana Olsen Rodrigues
LRLuiz Sérgio Raposo
Luiz Sérgio Raposo
JMJosé Victor Maníglia
José Victor Maníglia
EGEny Maria Goloni-Bertollo
Eny Maria Goloni-Bertollo

1 June 2011 in Molecular Biology Reports
Verified
Journal Article
Closed access
PDF file
LALidia Maria Rebolho Batista Arantes
Lidia Maria Rebolho Batista Arantes
AGAna Lívia Silva Galbiatti-Dias
Ana Lívia Silva Galbiatti-Dias
MRMariangela Torreglosa Ruiz
Mariangela Torreglosa Ruiz
LRLuiz Sérgio Raposo
Luiz Sérgio Raposo
JMJosé Victor Maniglia
José Victor Maniglia
EGEny Maria Goloni-Bertollo
Eny Maria Goloni-Bertollo

1 January 2010 in Revista da Associação Médica Brasileira
Verified
Journal Article
Open access
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CLCássia Veridiana Dourado Leme
Cássia Veridiana Dourado Leme
LRLuis Sérgio Raposo
Luis Sérgio Raposo
MRMariangela Torreglosa Ruiz
Mariangela Torreglosa Ruiz
JBJoice Matos Biselli
Joice Matos Biselli
AGAna Lívia Silva Galbiatti-Dias
Ana Lívia Silva Galbiatti-Dias
EGEny Maria Goloni-Bertollo
Eny Maria Goloni-Bertollo
OBJETIVO: Estabelecer o perfil clínico e demográfico bem como identificar os fatores de risco entre os pacientes com câncer de cabeça e pescoço e relacioná-los ao polimorfismo dos genes GSTT1 e GSTM1. MÉTODOS: Foram estudados 100 pacientes com carcinoma espinocelular de cabeça e pescoço e 100 indivíduos sem história de neoplasia. A análise molecular foi realizada pela técnica de PCR multiplex. Para a análise estatística, os dados foram tabulados e comparados pelo teste exato de Fisher. Foi também utilizado o teste do Qui quadrado e de regressão logística múltipla. RESULTADOS: Há predomínio de indivíduos tabagistas (OR= 5,32; IC95%= 2,04-13,86; p=0,0006), etilistas (OR= 5,04; IC95%= 2,19-11,59; p= 0,0001) em pacientes com neoplasia de cabeça e pescoço. Foi identificado genótipo nulo do gene GSTT1 em 47% dos pacientes e 41% dos controles (OR= 0,67; IC 95%= 0,34-1,35; p= 0,2648). Da mesma forma, identificou-se o genótipo nulo do gene GSTM1 em 66% dos pacientes e 75% dos controles (OR= 2,25; IC95%= 1,05-4,84; p= 0,0368). A análise dos genótipos combinados demonstrou associação entre GSTM1*0/GSTT1 e a ocorrência de carcinoma de cabeça e pescoço (OR= 7,64; IC 95%= 1,72-34,04; p= 0,0076). A análise dos parâmetros clínicos mostrou que é possível identificar associação entre genótipo GSTT1 nulo e neoplasia na laringe, o inverso ocorrendo com este genótipo e a faringe. CONCLUSÃO: Em nosso estudo foi possível estabelecer a associação entre a nulidade do genótipo GSTM1 e dos genótipos combinados GSTT1/GSTM1 *0 ([ ] / [-] a ocorrência de câncer de cabeça e pescoço. OBJECTIVE: To establish the clinical and demographic profile and identify risk factors among patients with head and neck cancer and relate them to the polymorphism of GSTT1 and GSTM1. METHODS: One hundred patients with head and neck cancer and 100 control group individuals without history of neoplasm were analyzed. . The molecular analysis were made by multiplex polymerase chain reaction. For statistical analysis, data were tabulated and compared by the Fisher’s exact test, the Chi-square test and multiple logistic regression were also used. RESULTS: There was prevalence of smokers (OR = 5.32, CI 95% CI = 2.04-13.86 p = 0.0006), alcohol drinkers (OR = 5.04, CI 95% = 2.19-11.59 p = 0.0001) in head and neck cancer patients . The GSTT1 null genotype was found in 47% of the patient and 41% of the control group (OR = 0.67; CI 95%= 0.34-1.35; p = 0.2648). Likewise , the GSTM1 null genotype was found in 66% of the patient and 75% of the control group (OR = 2.25; CI 95%= 1.05 - 4.84; p = 0.0368). The combined GSTT1 and GSTM1 gene null genotype shown association between GSTM1*0/GSTT1 and occurrence of head and neck carcinoma (OR = 7.64; CI 95%= 1.72-34.04; p = 0.0076). Analysis of clinical-pathological features showed association between GSTT1 null genotype and larynx, the inverse relation between this genotype and pharynx. CONCLUSION: In our study it was possible to establish association between GSTM1 null genotypes and head and neck cancer