scholarly journals Su1125 Tumor Suppressive Gene p-53 and Cell Proliferation Marker KI-67 in Children With Eosinophilic Esophagitis

2012 ◽  
Vol 142 (5) ◽  
pp. S-431
Author(s):  
Awni Al-Subu ◽  
Krista L. Denning ◽  
Jenna Maynard ◽  
Pamela Thompson ◽  
Sarah E. Wellman ◽  
...  
2002 ◽  
Vol 33 (2) ◽  
pp. 170-174 ◽  
Author(s):  
Gail Amir ◽  
Josephine Issakov ◽  
Isaac Meller ◽  
Erwin Sucher ◽  
Amos Peyser ◽  
...  

2006 ◽  
Vol 33 (2) ◽  
pp. 203-209 ◽  
Author(s):  
Catherine Hou ◽  
Zhude Tu ◽  
Robert Mach ◽  
Hank F. Kung ◽  
Mei-Ping Kung

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Ramón Gil Carreón-Burciaga ◽  
Rogelio González-González ◽  
Nelly Molina-Frechero ◽  
Ronell Bologna-Molina

Cell proliferation assays are performed using antibodies against nuclear proteins associated with DNA replication. These nuclear proteins have gained special interest to predict the biological and clinical behaviors of various tumors. The aim of this study was to analyze the presence of Ki-67 protein and the minichromosome maintenance-2 (MCM2) and maintenance-3 (MCM3) proteins in ameloblastoma.Materials and Methods. Cell proliferation marker expression levels were assessed via immunohistochemistry in 111 ameloblastoma cases (72 unicystic ameloblastoma samples, 38 solid/multicystic ameloblastoma samples, and 1 ameloblastic carcinoma). The label index was performed as described previously.Results.MCM2 and MCM3 showed higher proliferation indexes in all variants of ameloblastoma compared to the classic marker Ki-67. No correlation between the proliferation index and the clinical and protein expression data was observed.Conclusion.The results suggest that clinical features do not directly affect tumor cell proliferation. Moreover, the high levels of cellular proliferation of MCM2 and MCM3 compared with Ki-67 may indicate that MCM2 and MCM3 are more sensitive markers for predicting the growth rate and eventually might be helpful as a tool for predicting aggressive and recurrent behaviors in these tumors.


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