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1.
Pathol Oncol Res ; 19(2): 303-9, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23225158

ABSTRACT

The multiple myeloma SET domain (MMSET) involved in the t(4;14)(p16;q32) chromosomal translocation encodes a histone lysine methyltransferase. High expression of MMSET is common translocation in multiple myeloma (MM) and is associated with the worst prognosis. Recent studies have shown that overexpression of MMSET is significant in other tumor types compared to their normal tissues. However, little is known about its role in hepatocellular carcinoma (HCC). In these study we investigate the expression of MMSET in HCC and to make correlations with clinicopathologic features. Twenty-eight pairs of HCC and adjacent non-tumor tissues, and eight normal liver tissues were collected for MMSET detection by western blotting and real time-PCR analysis. Immunohistochemistry was used to determine the expression of MMSET in HCC and adjacent non-tumor tissues from 103 patients. Overexpression of MMSET was significantly associated with Edmondson stage, vascular invasion. Moreover, Kaplan-Meier curves showed that MMSET upregulated was associated with shorter overall survival and disease-free survival in HCC patient. In conclusion, our study demonstrates for the first time that overexpression of MMSET is an independent prognostic factor and is correlated with poor survival in HCC patients.


Subject(s)
Carcinoma, Hepatocellular/metabolism , Histone-Lysine N-Methyltransferase/genetics , Liver Neoplasms/genetics , Repressor Proteins/genetics , Carcinoma, Hepatocellular/genetics , Carcinoma, Hepatocellular/pathology , Disease-Free Survival , Female , Follow-Up Studies , Histone-Lysine N-Methyltransferase/biosynthesis , Histone-Lysine N-Methyltransferase/metabolism , Humans , Immunohistochemistry , Kaplan-Meier Estimate , Liver Neoplasms/metabolism , Liver Neoplasms/pathology , Male , Middle Aged , Prognosis , Repressor Proteins/biosynthesis , Repressor Proteins/metabolism , Up-Regulation
2.
Dig Dis Sci ; 54(11): 2410-7, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19101799

ABSTRACT

This study aims to investigate the expression and significance of EphA2 and EphrinA-1 in human gastric adenocarcinoma progression and prognosis. The expression of EphA2 and EphrinA-1 was detected in the cell lines and tissues of gastric adenocarcinoma. Different expression levels of EphA2 and EphrinA-1 were found in two cell lines. The expression of EphA2 and EphrinA-1 was significantly higher in gastric adenocarcinoma tissues than in normal tissues. Statistical analysis showed a significant correlation of EphA2 expression with the depth of tumor invasion, tumor-node-metastasis (TNM) stages, and lymph node metastasis. EphrinA-1 over-expression was significantly correlated with TNM stages and lymph node metastasis, while EphA2 expression was found to be an independent prognostic factor of postoperative gastric adenocarcinoma. In conclusion, the increased expression of EphA2 and EphrinA-1 plays an important role in the progression of human gastric adenocarcinoma, in which elevated EphA2 expression is an independent factor that indicates poor prognosis in postoperative gastric adenocarcinoma.


Subject(s)
Adenocarcinoma/metabolism , Ephrin-A1/metabolism , Receptor, EphA2/metabolism , Stomach Neoplasms/metabolism , Adenocarcinoma/mortality , Adenocarcinoma/pathology , Aged , Cell Line, Tumor , China/epidemiology , Female , Humans , Male , Middle Aged , Postoperative Period , Prognosis , Stomach/pathology , Stomach Neoplasms/mortality , Stomach Neoplasms/pathology
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