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Expression of E-cadherin and B-cell lymphoma 2 in oral cancer: A ratio-based planning for targeted therapy.

AbstractBACKGROUND:
Oral cancer is known to be governed by the antiapototic and loss of cell adhesion properties which dictate its progression.
AIM:
To study the immunexpression of E-cadherin and Bcl-2 in varying TNM stages and histopathological grades of OSCC.
MATERIALS AND METHODS:
11 cases of well differentiated, 10 cases of moderately differentiated and 11 cases of poorly differentiated OSCC were studied immunohistochemically using archival paraffin embedded tissue specimens.
STATISTICAL ANALYSIS:
Differences between the different variables were analyzed using ANOVA test, Kruskal-Wallis test and post hoc test followed by Bonferroni test. The resulting data was analyzed using SPSS software version 19.
RESULTS:
The expression of Bcl-2 and E cadherin immunopositivity was associated positively with tumor grade, high T category and Histopathological grades.
CONCLUSIONS:
The results of this study points to the significance of cell proliferation and invasion as a major determinant of prognosis in OSCC.
AuthorsNikita Gulati, Ajit Singh Rathore, Saurabh Juneja, Priyanka Rastogi
JournalIndian journal of dental research : official publication of Indian Society for Dental Research (Indian J Dent Res) 2017 Jan-Feb Vol. 28 Issue 1 Pg. 3-9 ISSN: 1998-3603 [Electronic] India
PMID28393810 (Publication Type: Journal Article)
Chemical References
  • BCL2 protein, human
  • Cadherins
  • Proto-Oncogene Proteins c-bcl-2
Topics
  • Cadherins (analysis, antagonists & inhibitors, genetics)
  • Carcinoma, Squamous Cell (drug therapy, genetics, immunology, pathology)
  • Cell Transformation, Neoplastic (drug effects, genetics, immunology, pathology)
  • DNA Mutational Analysis
  • Developing Countries
  • Humans
  • India
  • Molecular Targeted Therapy
  • Mouth Neoplasms (drug therapy, genetics, immunology, pathology)
  • Neoplasm Grading
  • Neoplasm Invasiveness
  • Neoplasm Staging
  • Proto-Oncogene Proteins c-bcl-2 (analysis, antagonists & inhibitors, genetics)

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