BRD4 inhibition suppresses cell growth, migration and invasion of salivary adenoid cystic carcinoma

被引:37
作者
Wang, Limei [1 ,2 ]
Wu, Xiuyin [2 ,3 ]
Wang, Ruolin [1 ,2 ]
Yang, Chengzhe [4 ,5 ]
Li, Zhi [1 ,2 ]
Wang, Cunwei [6 ]
Zhang, Fenghe [7 ]
Yang, Pishan [1 ,2 ]
机构
[1] Shandong Univ, Sch Stomatol, Dept Periodontol, 44-1 West Wen Hua Rd, Jinan 250012, Shandong, Peoples R China
[2] Shandong Prov Key Lab Oral Tissue Regenerat, Jinan 250012, Shandong, Peoples R China
[3] Laiwu City Peoples Hosp, Dept Stomatol, Laiwu 271100, Shandong, Peoples R China
[4] Shandong Univ, Qilu Hosp, Dept Oral & Maxillofacial Surg, Jinan 250012, Shandong, Peoples R China
[5] Shandong Univ, Inst Stomatol, Jinan 250012, Shandong, Peoples R China
[6] Shandong Univ, Sch Stomatol, Dept Prosthodont, Jinan 250012, Shandong, Peoples R China
[7] Shandong Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, 44-1 West Wen Hua Rd, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Salivary adenoid cystic carcinoma; BRD4; inhibition; Proliferation; Migration; Epithelial-mesenchymal transition; BET BROMODOMAIN INHIBITION; EPITHELIAL-MESENCHYMAL TRANSITION; HISTONE DEACETYLASE INHIBITOR; COLORECTAL-CANCER; TRANSCRIPTION FACTORS; DISTANT METASTASIS; GENE-EXPRESSION; MYC EXPRESSION; PROTEIN BRD4; JQ1;
D O I
10.1186/s40659-017-0124-9
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 mu M. 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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页数:13
相关论文
共 49 条
[1]   BRD4-targeted therapy induces Myc-independent cytotoxicity in Gnaq/11-mutatant uveal melanoma cells [J].
Ambrosini, Grazia ;
Sawle, Ashley D. ;
Musi, Elgilda ;
Schwartz, Gary K. .
ONCOTARGET, 2015, 6 (32) :33397-33409
[2]   Therapeutic targeting of BET bromodomain proteins in castration-resistant prostate cancer [J].
Asangani, Irfan A. ;
Dommeti, Vijaya L. ;
Wang, Xiaoju ;
Malik, Rohit ;
Cieslik, Marcin ;
Yang, Rendong ;
Escara-Wilke, June ;
Wilder-Romans, Kari ;
Dhanireddy, Sudheer ;
Engelke, Carl ;
Iyer, Mathew K. ;
Jing, Xiaojun ;
Wu, Yi-Mi ;
Cao, Xuhong ;
Qin, Zhaohui S. ;
Wang, Shaomeng ;
Feng, Felix Y. ;
Chinnaiyan, Arul M. .
NATURE, 2014, 510 (7504) :278-+
[3]   BET inhibitors induce apoptosis through a MYC independent mechanism and synergise with CDK inhibitors to kill osteosarcoma cells [J].
Baker, Emma K. ;
Taylor, Scott ;
Gupte, Ankita ;
Sharp, Phillip P. ;
Walia, Mannu ;
Walsh, Nicole C. ;
Zannettino, Andrew C. W. ;
Chalk, Alistair M. ;
Burns, Christopher J. ;
Walkley, Carl R. .
SCIENTIFIC REPORTS, 2015, 5
[4]   Perineural invasion in adenoid cystic carcinoma of the salivary glands: A valid prognostic indicator? [J].
Barrett, A. William ;
Speight, Paul M. .
ORAL ONCOLOGY, 2009, 45 (11) :936-940
[5]   The Bromodomain BET Inhibitor JQ1 Suppresses Tumor Angiogenesis in Models of Childhood Sarcoma [J].
Bid, Hemant K. ;
Phelps, Doris A. ;
Xaio, Linlin ;
Guttridge, Denis C. ;
Lin, Jiayuh ;
London, Cheryl ;
Baker, Laurence H. ;
Mo, Xiaokui ;
Houghton, Peter J. .
MOLECULAR CANCER THERAPEUTICS, 2016, 15 (05) :1018-1028
[6]   Long noncoding RNA SPRY4-IT1 promotes malignant development of colorectal cancer by targeting epithelial-mesenchymal transition [J].
Cao, Dong ;
Ding, Qiong ;
Yu, Wubin ;
Gao, Ming ;
Wang, Yilian .
ONCOTARGETS AND THERAPY, 2016, 9 :5417-5425
[7]   Dissemination and growth of cancer cells in metastatic sites [J].
Chambers, AF ;
Groom, AC ;
MacDonald, IC .
NATURE REVIEWS CANCER, 2002, 2 (08) :563-572
[8]   SOD2 deregulation enhances migration, invasion and has poor prognosis in salivary adenoid cystic carcinoma [J].
Chang, Boyang ;
Yang, Hang ;
Jiao, Yuan ;
Wang, Kefeng ;
Liu, Zhonghua ;
Wu, Peihong ;
Li, Su ;
Wang, Anxun .
SCIENTIFIC REPORTS, 2016, 6
[9]   Synergistic action of master transcription factors controls epithelial-to-mesenchymal transition [J].
Chang, Hongyuan ;
Liu, Yuwei ;
Xue, Mengzhu ;
Liu, Haiyue ;
Du, Shaowei ;
Zhang, Liwen ;
Wang, Peng .
NUCLEIC ACIDS RESEARCH, 2016, 44 (06) :2514-2527
[10]   Involvement of DNMT 3B promotes epithelial-mesenchymal transition and gene expression profile of invasive head and neck squamous cell carcinomas cell lines [J].
Chen, Li-Hsuen ;
Hsu, Wen-Lin ;
Tseng, Yen-Ju ;
Liu, Dai-Wei ;
Weng, Ching-Feng .
BMC CANCER, 2016, 16