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Chinese Journal of Oncology ; (12): 351-355, 2013.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-284177

RESUMO

<p><b>OBJECTIVE</b>To explore the association between methylation of cystathionine-beta-synthase (CBS) promoter and clinicopathological features in colorectal cancer.</p><p><b>METHODS</b>Bisulfate sequencing PCR, real-time RT-PCR, and immunohistochemistry were used to investigate the methylation of CpG island in CBS promoter of 95 sporadic colorectal cancers. Software SPSS PASW Statistics was used to analyze the data of the hypermethylation levels in the malignant tissues and the correlation with pathological parameters and clinical outcome.</p><p><b>RESULTS</b>Methylation levels in tumor tissue of patients [(64.9 ± 14.3)%]with colorectal cancer were significantly higher than that in normal tissues[(27.5 ± 13.1)%, P < 0.001]. The CBS mRNA levels in the hypomethylation group (7.22 ± 1.91) were significantly higher than that in the hypermethylation group (2.78 ± 1.12, P < 0.01). Univariate analysis showed that age, pT stage, pN stage, liver metastases, pTNM stage, and CBS hypermethylation level significantly correlated with the survival and recurrence rates of colorectal cancer patients (All P < 0.05). Multivariate analysis showed that CBS hypermethylation level and liver metastasis were independent factors significantly correlated with the recurrence rate and overall survival of the patients (All P < 0.05).</p><p><b>CONCLUSIONS</b>Our study indicates that methylation of CpG island in CBS promoter is correlated with the occurrence and progression of colorectal cancer and plays a role in its tumorigenesis. It might serve as a useful marker for early diagnosis, targeted therapy and prediction of prognosis in colorectal cancer.</p>


Assuntos
Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adenocarcinoma , Genética , Metabolismo , Patologia , Biomarcadores Tumorais , Genética , Metabolismo , Neoplasias Colorretais , Genética , Metabolismo , Patologia , Ilhas de CpG , Genética , Cistationina beta-Sintase , Genética , Metabolismo , Metilação de DNA , Seguimentos , Neoplasias Hepáticas , Gradação de Tumores , Recidiva Local de Neoplasia , Estadiamento de Neoplasias , Prognóstico , Regiões Promotoras Genéticas , Genética , RNA Mensageiro , Metabolismo
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