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BRD4 inhibition suppresses cell growth, migration and invasion of salivary adenoid cystic carcinoma
Wang, Limei; Wu, Xiuyin; Wang, Ruolin; Yang, Chengzhe; Li, Zhi; Wang, Cunwei; Zhang, Fenghe; Yang, Pishan.
  • Wang, Limei; Shandong University. School of Stomatology. Department of Periodontology. Jinan. CN
  • Wu, Xiuyin; Shandong Provincial Key Laboratory of Oral Tissue Regeneration. Jinan. CN
  • Wang, Ruolin; Shandong University. School of Stomatology. Department of Periodontology. Jinan. CN
  • Yang, Chengzhe; Shandong University. Qilu Hospital, and Institute of Stomatology. Department of Oral & Maxillofacial Surgery. Jinan. CN
  • Li, Zhi; Shandong University. School of Stomatology. Department of Periodontology. Jinan. CN
  • Wang, Cunwei; Shandong University. School of Stomatology. Department of Prosthodontics. Jinan. CN
  • Zhang, Fenghe; Shandong University. School of Stomatology. Department of Oral & Maxillofacial Surgery. Jinan. CN
  • Yang, Pishan; Shandong University. School of Stomatology. Department of Periodontology. Jinan. CN
Biol. Res ; 50: 19, 2017. graf
Artículo en Inglés | LILACS | ID: biblio-950871
ABSTRACT
BACKGROUND: Bromodomain-containing protein 4 (BRD4) inhibition is a new therapeutic strategy for many malignancies. In this study, we aimed to explore the effect of BRD4 inhibition by JQ1 on in vitro cell growth, migration and invasion of salivary adenoid cystic carcinoma (SACC). METHODS: The human normal epithelial cells and SACC cells (ACC-LM and ACC-83) were treated with JQ1 at concentrations of 0, 0.1, 0.5 or 1 µM. Cell Counting Kit-8 (CCK-8) assay was performed to evaluate cell proliferation. Cell apoptosis and cell cycle distribution was evaluated by Flow cytometry. Immunofluorescence staining was used to examine the expression of BRD4 in SACC cells. The quantitative real-time polymerase chain reaction (qRT-PCR) assay and western blot assay were performed to examine messenger RNA (mRNA) and protein levels in SACC cells. Wound- healing assay and transwell assay were used to evaluate the activities of migration and invasion of SACC cells. RESULTS: JQ1 exhibits no adverse effects on proliferation, cell cycle and cell apoptosis of the normal human epithelial cells, while suppressed proliferation and cell cycle, and induced apoptosis of SACC cells, down-regulated the mRNA and protein levels of BRD4 in SACC cells, meanwhile reduced protein expressions of c-myc and BCL-2, two known target genes of BRD4. Moreover, JQ1 inhibited SACC cell migration and invasion by regulating key epithelial-mesenchymal transition (EMT) characteristics including E-cadherin, Vimentin and Twist. CONCLUSIONS: BRD4 is an important transcription factor in SACC and BRD4 inhibition by JQ1 may be a new strategy for SACC treatment.
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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Azepinas / Factores de Transcripción / Triazoles / Neoplasias de las Glándulas Salivales / Proteínas Nucleares / Movimiento Celular / Carcinoma Adenoide Quístico / Proliferación Celular / Invasividad Neoplásica Límite: Humanos Idioma: Inglés Revista: Biol. Res Asunto de la revista: Biologia Año: 2017 Tipo del documento: Artículo País de afiliación: China Institución/País de afiliación: Shandong Provincial Key Laboratory of Oral Tissue Regeneration/CN / Shandong University/CN

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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Azepinas / Factores de Transcripción / Triazoles / Neoplasias de las Glándulas Salivales / Proteínas Nucleares / Movimiento Celular / Carcinoma Adenoide Quístico / Proliferación Celular / Invasividad Neoplásica Límite: Humanos Idioma: Inglés Revista: Biol. Res Asunto de la revista: Biologia Año: 2017 Tipo del documento: Artículo País de afiliación: China Institución/País de afiliación: Shandong Provincial Key Laboratory of Oral Tissue Regeneration/CN / Shandong University/CN