题名 | I-BET726 suppresses human skin squamous cell carcinoma cell growth in vitro and in vivo |
作者 | |
发表日期 | 2020-05-05 |
发表期刊 | CELL DEATH & DISEASE 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
其他关键词 | PANCREATIC-CANCER CELLS ; SPHINGOSINE KINASE-1 ; PROTEIN PHOSPHATASE ; TREATMENT OPTIONS ; TARGETED THERAPY ; INHIBITION ; RESISTANCE ; APOPTOSIS ; BRD4 ; RAS/RAF/MEK/ERK |
摘要 | Bromodomain-containing protein 4 (BRD4) is a potential therapeutic target of skin squamous cell carcinoma (SCC). I-BET726 is a novel BRD4 inhibitor. Its potential effect in skin SCC cells was tested in the present study. We show that I-BET726 potently inhibited survival, proliferation, cell cycle progression, and migration in established (A431/SCC-9/SCC-12/SCC-13 lines) and primary human skin SCC cells. I-BET726 induced significant apoptosis activation in skin SCC cells. It was more efficient in inhibiting skin SCC cells than known BRD4 inhibitors (JQ1, CPI203, and AZD5153). I-BET726 not only downregulated BRD4-regulated proteins (c-Myc, Bcl-2, and cyclin D1), but also inhibited sphingosine kinase 1 (SphK1) and Akt signalings in SCC cells. Restoring Akt activation, by a constitutively active S473D mutant Akt1 (caAkt1), partially inhibited I-BET726-induced cytotoxicity in A431 cells. In vivo, I-BET726 oral administration potently inhibited A431 xenograft growth in severe combined immunodeficient mice. Downregulation of BRD4-regulated proteins and inhibition of the SphK1-Akt signaling were detected in I-BET726-treated A431 xenograft tumor tissues. Together, I-BET726 inhibits skin SCC cell growth in vitro and in vivo. |
资助项目 | National Natural Science FoundationNational Natural Science Foundation of China (NSFC) [81773192, 81472786, 81902715, 81774109]; Foundation of Tumor Clinical and Basic Research Team of Affiliated Kunshan Hospital of Jiangsu University [KYC005]; Jiangsu Province Youth Medical Talents Project [QNRC2016527]; Jiangsu Province 333 Project Research Projects [2016-III-0367]; Kunshan Science and Technology Program [KS18057]; Jiangsu University Clinical Medical Science and Technology Development Fund [JLY20180012]; Natural Science Foundation of Jiangsu ProvinceNatural Science Foundation of Jiangsu Province [BK20171248, BK20180195]; Scientific Research Program for Young Talents of China National Nuclear Corporation (Shang Cai) |
出版者 | NATURE PUBLISHING GROUP |
出版地 | LONDON |
ISSN | 2041-4889 |
卷号 | 11期号:5页码:318 |
DOI | 10.1038/s41419-020-2515-z |
页数 | 12 |
WOS类目 | Cell Biology |
WOS研究方向 | Cell Biology |
WOS记录号 | WOS:000532354400003 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 32371868 |
PMC记录号 | PMC7200671 |
SCOPUSEID | 2-s2.0-85084221543 |
通讯作者地址 | [Guo, Hailei]Department of Burn and Plastic Surgery,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,China |
Scopus学科分类 | Immunology;Cellular and Molecular Neuroscience;Cell Biology;Cancer Research |
TOP期刊 | TOP期刊 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/7305 |
专题 | 第一临床医学院(信息与工程学院)、附属第一医院_外科学_整形外科 附属第一医院 |
通讯作者 | Guo, Hailei |
作者单位 | 1.Department of Burn and Plastic Surgery,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,China; 2.Department of Radiotherapy and Oncology,Affiliated Kunshan Hospital of Jiangsu University,Kunshan,China; 3.Department of Radiotherapy and Oncology,the Second Affiliated Hospital of Soochow University,Suzhou,China |
第一作者单位 | 附属第一医院; 第一临床医学院(信息与工程学院)、附属第一医院 |
通讯作者单位 | 附属第一医院; 第一临床医学院(信息与工程学院)、附属第一医院 |
第一作者的第一单位 | 附属第一医院 |
推荐引用方式 GB/T 7714 | Liu, Zhengjun,Li, Ping,Yang, Yong-qiang,et al. I-BET726 suppresses human skin squamous cell carcinoma cell growth in vitro and in vivo[J]. CELL DEATH & DISEASE,2020,11(5):318. |
APA | Liu, Zhengjun., Li, Ping., Yang, Yong-qiang., Cai, Shang., Lin, Xiangwei., ... & Guo, Hailei. (2020). I-BET726 suppresses human skin squamous cell carcinoma cell growth in vitro and in vivo. CELL DEATH & DISEASE, 11(5), 318. |
MLA | Liu, Zhengjun,et al."I-BET726 suppresses human skin squamous cell carcinoma cell growth in vitro and in vivo".CELL DEATH & DISEASE 11.5(2020):318. |
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