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1.
Oncol Lett ; 13(5): 3087-3099, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28521414

RESUMO

The aim of the present study was to determine the association between sirtuin 1 (SIRT1), fibroblast growth factor receptor 2 (FGFR2) and signal transducer and activator of transcription 3 (STAT3) polymorphisms, and pituitary adenoma (PA) development, invasiveness, hormonal activity and recurrence. The present study included 143 patients with a diagnosis of PA. The reference group involved 808 healthy subjects. The genotyping of SIRT1 rs12778366, FGFR2 rs2981582 and STAT3 rs744166 was performed using the quantitative polymerase chain reaction method. The SIRT1 rs12778366 polymorphism analysis in the overall group revealed differences in the genotype distribution between patients with PA and control group subjects. The rs12778366 T/C genotype was observed to be different in non-invasive, non-recurrent and inactive PA subgroups compared with the control group, while the C/C genotype was observed to be different in invasive, recurrent and active PA subgroups compared with the control group. STAT3 rs744166 polymorphism analysis in the overall group revealed differences in the genotype distribution between patients with PA and the control groups. The rs744166 G/G genotype was observed to be different in invasive, non-recurrent and active PA subgroups compared with the control group, while the rs744166 A/A genotype was observed to be different in the active PA subgroup compared with the control group, and was also different in terms of invasiveness and recurrence in PA subgroups. The present study demonstrated that SIRT1 rs12778366 is associated with pituitary adenoma development while STAT3 rs744166 is associated with PA invasiveness, hormonal activity and recurrence.

2.
Dis Markers ; 2017: 5839528, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28194042

RESUMO

Purpose. To determine if the MMP-9 genotype has an influence on development of pituitary adenoma (PA). Methodology. The study enrolled n = 86 patients with PA and n = 526 healthy controls (reference group). The genotyping of MMP-9 was carried out using the real-time polymerase chain reaction method. Results. Our data demonstrated that the MMP-9 (-1562) C/C genotype was more frequent in PA group than in healthy controls (81.4% versus 64.6%, p = 0.002); C/C genotype was more frequently present in PA females compared to healthy control females, 81.5% versus 64.6%, p = 0.018, as well. MMP-9 (-1562) C/C genotype was frequently observed for all subgroups: noninvasive and invasive, nonrecurrence, and inactive PA compared to healthy controls: 81.8% versus 64.6%, p = 0.021; 81.0% versus 64.6%, p = 0.041; 81.8% versus 64.6%, p = 0.005; 100.0% versus 64.6%, p < 0.001, respectively. MMP-9 (-1562) C/C genotype was more frequent in inactive PA compared to active PA: 100.0% versus 71.4%; p < 0.001. Conclusion. MMP-9 (-1562) C/C genotype plays a role in nonrecurrence, inactive, and invasive as well as in nonivasive PA development.


Assuntos
Adenoma/genética , Metaloproteinase 9 da Matriz/genética , Neoplasias Hipofisárias/genética , Polimorfismo de Nucleotídeo Único , Adenoma/patologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos de Casos e Controles , Feminino , Predisposição Genética para Doença , Humanos , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Recidiva Local de Neoplasia/genética , Neoplasias Hipofisárias/patologia , Adulto Jovem
3.
Acta Med Litu ; 24(4): 177-190, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29487481

RESUMO

BACKGROUND: The pathogenesis of pituitary adenoma (PA) is complex and poorly understood. It is thought that PA has a multifactorial aetiology; genetic factors also have an impact on PA development. Since MMP1 and FGFR4 genes play an important role in tumour growth, differentiation and progression, we decided to determine if the frequency of the genotypes of MMP-1 and FGFR4-R388 polymorphisms influence the development of PA. MATERIALS AND METHODS: The study enrolled n = 100 patients with PA and n = 200 healthy controls (reference group). The genotyping tests of MMP-1 and FGFR4-R388 were carried out using the real-time polymerase chain reaction (PCR) method. RESULTS: The polymorphism in the MMP-1 gene 1G/1G genotype was more frequent in the group of invasive PA than in the control group: 28.6% vs. 16.5%, p = 0.044. The 1G/2G genotype was more frequent in females of the control group compared to PA group females: 50.3% vs. 30.8%, p = 0.011. The polymorphism in the MMP-1 gene 1G/1G genotype was more frequent in the active PA group than in the control group: 28.4% vs. 16.5%, p = 0.044. FGFR4-R388 did not play any predominant role in PA development. CONCLUSION: The MMP-1 gene 1G/1G may play a role in invasive and active PA development.

4.
Medicina (Kaunas) ; 45(9): 693-8, 2009.
Artigo em Lituano | MEDLINE | ID: mdl-19834305

RESUMO

The most common genetically determined cause of multiple pituitary hormone deficiency is PROP-1 gene mutation. PROP-1 is a transcription factor involved in the development of pituitary gland and affects hormonal synthesis of anterior pituitary. The aim of our study was to evaluate radiological aspects of the pituitary region in patients with PROP-1 gene mutation. Pituitary imaging studies were performed in 12 patients with a confirmed PROP-1 gene mutation. Pituitary hyperplasia was found in 5 (42%) and pituitary hypoplasia in 4 (33%) patients. Changes in pituitary size were not associated with the type of PROP-1 gene mutation.


Assuntos
Proteínas de Homeodomínio/genética , Hipopituitarismo/genética , Hipopituitarismo/patologia , Mutação , Hipófise/patologia , Adolescente , Encéfalo/diagnóstico por imagem , Criança , Pré-Escolar , Feminino , Hormônio do Crescimento Humano/deficiência , Humanos , Hiperplasia , Hipopituitarismo/diagnóstico , Hipopituitarismo/diagnóstico por imagem , Hipopituitarismo/fisiopatologia , Recém-Nascido , Imageamento por Ressonância Magnética , Masculino , Hipófise/diagnóstico por imagem , Hormônios Hipofisários/deficiência , Tomografia Computadorizada Espiral , Fatores de Transcrição
5.
Medicina (Kaunas) ; 38(2): 135-9, 2002.
Artigo em Lituano | MEDLINE | ID: mdl-12474729

RESUMO

The purpose of this study was to determine the character of MR findings in the cases of intratumoral hemorrhage within pituitary adenomas, and to correlate them with surgery and CT. In our study we included 86 patients with pituitary adenomas, who underwent surgery at the Clinic of Neurosurgery at Kaunas Medical University Hospital. In 23% (n = 20) of cases with MR evidence of intratumoral hemorrhage the variety of focal MR signal changes was observed in dependence of hemoglobin degradation process and accumulation of blood products. CT demonstrated only 10% (n = 2) of cases with acute intratumoral hemorrhage. The nonspecific hypodensities within pituitary adenomas were observed in 35% (n = 7) cases. Fifty-five percent (n = 11) of cases demonstrated no focal changes. All surgically discovered hemorrhages within pituitary adenomas were clinically asymptomatic.


Assuntos
Adenoma/diagnóstico , Hemorragia/diagnóstico , Imageamento por Ressonância Magnética , Neoplasias Hipofisárias/diagnóstico , Tomografia Computadorizada por Raios X , Adenoma/complicações , Adenoma/diagnóstico por imagem , Adenoma/cirurgia , Adulto , Feminino , Hemoglobinas/análise , Hemorragia/diagnóstico por imagem , Hemorragia/etiologia , Hemossiderina/análise , Humanos , Masculino , Metemoglobina/análise , Pessoa de Meia-Idade , Oxiemoglobinas/análise , Neoplasias Hipofisárias/complicações , Neoplasias Hipofisárias/diagnóstico por imagem , Neoplasias Hipofisárias/cirurgia , Fatores de Tempo
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