EXPRESSION OF TERATOCARCINOMA-DERIVED GROWTH FACTOR-1 (CRIPTO-1) IN EPITHELIAL ODONTOGENIC LESIONS
Objective: To evaluate the immunohistochemical expression of CRIPTO-1 in odontogenic cysts and tumors. Study Design: Thirty ameloblastomas, 30 keratocysts, 30 dentigerous cysts, and 2 ameloblastic carcinomas were evaluated using the biotin-free immunoperoxidase technique. The immunohistochemical exp...
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Published in: | Oral surgery, oral medicine, oral pathology and oral radiology Vol. 130; no. 3; p. e245 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier Inc
01-09-2020
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Online Access: | Get full text |
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Summary: | Objective: To evaluate the immunohistochemical expression of CRIPTO-1 in odontogenic cysts and tumors. Study Design: Thirty ameloblastomas, 30 keratocysts, 30 dentigerous cysts, and 2 ameloblastic carcinomas were evaluated using the biotin-free immunoperoxidase technique. The immunohistochemical expression was analyzed from the immunoreactive score (IRS). Kruskal Wallis and Mann-Whitney U tests were performed for statistical analysis (P ≤ .05). Results: Ages ranged from 9 to 75 years, with female gender being the most prevalent (n = 49; 53.3%). The mandible was the most affected anatomic site (n = 69; 75.0%). Immunoexpression of CRIPTO-1 was observed in all cases of ameloblastoma, keratocyst, and ameloblastic carcinoma; however, 9 cases (30%) of dentigerous cysts were negative. Expression scores were higher in cases of ameloblastomas, keratocysts, and ameloblastic carcinomas (median, 8-11) compared with cases of dentigerous cysts (median, 2) being statistically significant (P < .001). Conclusion: CRIPTO-1 is critically important in the progression of some tumor types because it is related to the transforming growth-Factor-beta (TGFβ) and epidermal growth factor receptor (EGFR) pathways. The high expression of CRIPTO-1 in more aggressive odontogenic lesions suggests that this molecule may be involved in the activation of important pathways related to the pathogenesis of these lesions. |
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ISSN: | 2212-4403 2212-4411 |
DOI: | 10.1016/j.oooo.2020.04.634 |