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Monoamine oxidase B inhibits epithelial-mesenchymal transition and trigger apoptosis via targeting ERK1/2 signaling pathway in head and neck squamous cell carcinoma.
Qi, Yibo; Shao, Weihua; Gao, Jing; Ni, Nan; Xue, Feifei; Wang, Tianxiao; Wang, Yuli; Fan, Yi; Yuan, Hua.
Afiliación
  • Qi Y; Jiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
  • Shao W; Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Stomatology, Nanjing Medical University, Nanjing, China.
  • Gao J; Department of Pharmacology, Neuroprotective Drug Discovery Center, Nanjing Medical University, Nanjing, China.
  • Ni N; Jiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
  • Xue F; Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Stomatology, Nanjing Medical University, Nanjing, China.
  • Wang T; Department of Pharmacology, Neuroprotective Drug Discovery Center, Nanjing Medical University, Nanjing, China.
  • Wang Y; Department of Pharmacology, Neuroprotective Drug Discovery Center, Nanjing Medical University, Nanjing, China.
  • Fan Y; Jiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, China.
  • Yuan H; Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Stomatology, Nanjing Medical University, Nanjing, China.
Head Neck ; 46(8): 2031-2041, 2024 08.
Article en En | MEDLINE | ID: mdl-38379404
ABSTRACT

BACKGROUND:

Monoamine oxidase B (MAOB), a flavin monoamine oxidase, regulates biogenic and xenobiotic amine oxidative deaminization. We demonstrate MAOB expression in head and neck epithelium and its biological importance in head and neck squamous cell carcinoma (HNSCC) development.

METHODS:

First, we found a possible MAOB downregulation in HNSCC using bioinformatic analysis. Second, we validated MAOB expression changes in vitro and assessed its tumorigenicity in HNSCC. Finally, preclinical xenograft models further confirmed our findings.

RESULTS:

Results proved that MAOB was significantly reduced in HNSCC tissues and cell lines. By comparing MAOB localization in patient specimens, we found that epithelial basal cells express MAOB and that it changes throughout HNSCC development. We observed that MAOB overexpression inhibited HNSCC cell malignancy via lentiviral transfection. We additionally discovered that selegiline partly counter-regulated MAOB overexpression-induced phenotypes in HNSCC cells.

CONCLUSIONS:

We found that MAOB is a potent biomarker and a unique and essential indication of HNSCC carcinogenesis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Apoptosis / Transición Epitelial-Mesenquimal / Carcinoma de Células Escamosas de Cabeza y Cuello / Neoplasias de Cabeza y Cuello / Monoaminooxidasa Límite: Animals / Female / Humans / Male Idioma: En Revista: Head Neck Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma de Células Escamosas / Apoptosis / Transición Epitelial-Mesenquimal / Carcinoma de Células Escamosas de Cabeza y Cuello / Neoplasias de Cabeza y Cuello / Monoaminooxidasa Límite: Animals / Female / Humans / Male Idioma: En Revista: Head Neck Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: China