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NOTCH1 MUTATION FROM ADENOID CYSTIC CARCINOMA FROM THE SALIVARY GLANDS PRESENT A BETTER RESPONSE TO EPI-DRUG THERAPY
Adenoid cystic carcinoma from the salivary glands (ACC-SG) is characterized by slow-growing and metastatic potential. Also, they are resistant to chemotherapy, and mutations in NOTCH1 and MYB suggest a poor prognosis. Objective: Here we decided to test the efficiency of a novel histone deacetylase i...
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Published in: | Oral surgery, oral medicine, oral pathology and oral radiology oral medicine, oral pathology and oral radiology, 2020-09, Vol.130 (3), p.e283-e283 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | Adenoid cystic carcinoma from the salivary glands (ACC-SG) is characterized by slow-growing and metastatic potential. Also, they are resistant to chemotherapy, and mutations in NOTCH1 and MYB suggest a poor prognosis. Objective: Here we decided to test the efficiency of a novel histone deacetylase inhibitor (HDACi), entinostat, in patient-derived xenografts (PDX) of ACC-SG (ACCX9, ACCM1, ACCX6). Study Design: PDX tumors were divided into vehicle, entinostat, cisplatin, and entinostat/cisplatin. Then, tumor growth inhibition (TGI) was calculated for each tumor and frozen samples were processed for gene expression using NanoString and key markers using immunofluorescence. Results: All responded to combined therapy of entinostat/cisplatin and the overall TGI observed was 106%, 63%, and 38% for ACCX9, ACCM1, and ACCX6, respectively. Furthermore, we found that tumors with a better response to therapy had a low expression of Ki-67, p16 ink4, gamma-H2 AX, nuclear factor kappa B (NFkB), p300, and upregulation of caspase3, H3 K9, and acetyl-p53. Reduced expression of NOTCH1 was associated with better response to therapy whereas high levels of MYB were associated with reduced response. Conclusion: Overall, a subset of ACC-SG presenting with a NOTCH1 mutation had a better response to the new epigenetic therapy, and that ACC-SG is comprised of a heterogeneous group of tumors exhibiting distinct genetic and resistance behavior toward HDACi. |
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ISSN: | 2212-4403 2212-4411 |
DOI: | 10.1016/j.oooo.2020.04.784 |