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1.
Chinese Journal of Oncology ; (12): 31-34, 2012.
Article in Chinese | WPRIM | ID: wpr-335350

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the methylation levels of death-associated protein kinase (DAPK) in Uyghur female patients with different cervical lesions in Xinjiang, and to discuss the relationship of the expression and significance of DAPK in normal cervix, chronic cervicitis, cervical intraepithelial neoplasia (CINI, CIN II/III) and invasive cervical squamous cell carcinoma.</p><p><b>METHODS</b>30 cases of normal cervix and chronic cervicitis, 30 cases of CINI, 30 cases of CINII/III and 30 cases of cervical squamous cell carcinoma were tested by methylation specific PCR (MSP). Expressions of DAPK in 30 cases of normal cervix and chronic cervicitis, 30 cases of CINI, 30 cases of CINII/III and 30 cases of cervical squamous cell carcinoma were assayed using immunohistochemical SP staining.</p><p><b>RESULTS</b>The methylation rate of DAPK gene in normal cervix and chronic cervicitis was 3.33%, 10% in cervical intraepithelial neoplasia CINI, 36.7% in CINII/III, and 63.3% in invasive cervical squamous cell carcinoma. The methylation rate of DAPK in the SCC group was significantly higher than that in the other groups (P < 0.05). Aberrant promoter methylation of the DAPK gene was positively correlated with the degree of cervical lesions. The positive rate of DAPK protein in normal cervix and chronic cervicitis was 93.3%, 83.3% in cervical intraepithelial neoplasia CINI, 60.0% in CINII/III, and 33.3% in invasive cervical squamous cell carcinoma. The expression of DAPK in the SCC group was significantly lower than that in the other groups (P < 0.05). The positive rate of DAPK protein was negatively correlated with the degree of cervical lesions (r(s) = -0.603, P < 0.001).</p><p><b>CONCLUSIONS</b>Methylation of DAPK is involved in the cervical carcinogenesis and DAPK gene promoter methylation occurs in the early development of cervical cancer in Uyghur women in Xinjiang. Detection of DAPK gene methylation may provide a basis for use in early detection of cervical cancer. DAPK protein expression is decreasing even disappears along with the progression of cervical lesions.</p>


Subject(s)
Adult , Aged , Female , Humans , Middle Aged , Apoptosis Regulatory Proteins , Genetics , Metabolism , Calcium-Calmodulin-Dependent Protein Kinases , Genetics , Metabolism , Carcinoma, Squamous Cell , Genetics , Metabolism , Pathology , Uterine Cervical Dysplasia , Genetics , Metabolism , Pathology , China , Ethnology , DNA Methylation , Death-Associated Protein Kinases , Disease Progression , Promoter Regions, Genetic , Genetics , Uterine Cervical Neoplasms , Genetics , Metabolism , Pathology , Uterine Cervicitis , Genetics , Metabolism , Pathology
2.
Acta Academiae Medicinae Sinicae ; (6): 592-596, 2007.
Article in Chinese | WPRIM | ID: wpr-298776

ABSTRACT

<p><b>OBJECTIVE</b>To explore the relationship between human papillomavirus (HPV) 16 infection and the expression of p33(ING1b), human telomerase reverse transcriptase (hTERT) in cervical squamous cell carcinoma of Uygur Female in Xinjiang Uygur Autonomous Region.</p><p><b>METHODS</b>Polymerase chain reaction (PCR) and immunohistochemical methods were used to detect HPV16 infection and the expression of p33(ING1b) and hTERT in the normal control group (n=12), the patients with cervical intraepithelial neoplasm (CIN) (n=34), and the patients with cervical squamous cell carcinoma (SCC) (n=50).</p><p><b>RESULTS</b>In the cervical tissues of Uygur female, the HPV16 infection rate was 0 in control group, 22.2% in the CIN 1 group, 44.0% in CIN 2 & CIN 3 group, and 74.0% in SCC group (P = 0.000). The expression rate of p33(ING1b) decreased was 91.7% in control group, 77.7% in CIN 1 group, 68.0% in CIN 2 & CIN 3 group, and 36.0% in SCC group (P = 0. 000). The expression rate of hTERT was 50.0% in control group, 66.6% in CIN 1 group, 88.0% in CIN 2 & CIN 3 group, and 94.0% in SCC group (P = 0.000). In the cervical tissues of Uygur female, the HPV16 infection rate was negatively correlated with the expression of p33(ING1b) (r = -0.294, P = 0.004), and was positively correlated with the expression of hTERT (r = 0.286, P = 0.005). The expression of p33(ING1b) was negatively correlated with the expression of hTERT (r = -0.361, P = 0.000).</p><p><b>CONCLUSION</b>The infection of HPV 16 correlates with the decreased expression of p33(ING1b) and increased expression of hTERT in the cervical squamous cell carcinoma of Uygur female in Xinjiang.</p>


Subject(s)
Female , Humans , Carcinoma, Squamous Cell , Metabolism , Virology , Uterine Cervical Dysplasia , Metabolism , Virology , China , Human papillomavirus 16 , Inhibitor of Growth Protein 1 , Intracellular Signaling Peptides and Proteins , Nuclear Proteins , Papillomavirus Infections , Metabolism , Virology , Telomerase , Tumor Suppressor Proteins , Uterine Cervical Neoplasms , Metabolism , Virology
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