Suppr超能文献

由DD3启动子驱动的携带SPAG9 shRNA的溶瘤腺病毒提高了多西他赛治疗前列腺癌的疗效。

Oncolytic Adenovirus with SPAG9 shRNA Driven by DD3 Promoter Improved the Efficacy of Docetaxil for Prostate Cancer.

作者信息

Lu Meng, Wei Fu-Kun, Wu Chuang, Xu Zi-Yang, Mao Li-Jun, Yang Dong-Rong

机构信息

Department of Urology, The Second Affiliated Hospital of Soochow University, Suzhou 215004, Jiangsu Province, China.

Department of Urology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.

出版信息

J Oncol. 2022 Apr 30;2022:7918067. doi: 10.1155/2022/7918067. eCollection 2022.

Abstract

Prostate cancer (PCa) is a common malignant tumor of the male urinary system and ranks the second in the causes of tumor-related deaths. Differential display code 3 (DD3) is a noncoding gene that is specifically expressed in PCa. High expression of sperm-associated antigen 9 (SPAG9) is closely related to tumorigenesis of PCa, and SPAG9 is a therapeutic target for PCa. In this study, a new oncolytic adenovirus DD3-ZD55-SPAG9 was constructed by using DD3 promoter to enhance the efficacy and safety of adenovirus. The combined use of DD3-ZD55-SPAG9 and docetaxel showed that DD3-ZD55-SPAG9 significantly improved the anti-tumor efficacy of docetaxel in PCa both in vitro and in vivo. The mechanism was related to the induction of tumor cell apoptosis and the inhibition of tumor cell invasion. In conclusion, DD3-ZD55-SPAG9 combined with docetaxel is an effective strategy for PCa therapy.

摘要

前列腺癌(PCa)是男性泌尿系统常见的恶性肿瘤,在肿瘤相关死亡原因中排名第二。差异显示编码3(DD3)是一种在PCa中特异性表达的非编码基因。精子相关抗原9(SPAG9)的高表达与PCa的肿瘤发生密切相关,且SPAG9是PCa的治疗靶点。在本研究中,通过使用DD3启动子构建了一种新型溶瘤腺病毒DD3-ZD55-SPAG9,以提高腺病毒的疗效和安全性。DD3-ZD55-SPAG9与多西他赛联合使用表明,DD3-ZD55-SPAG9在体外和体内均显著提高了多西他赛对PCa的抗肿瘤疗效。其机制与诱导肿瘤细胞凋亡和抑制肿瘤细胞侵袭有关。总之,DD3-ZD55-SPAG9与多西他赛联合使用是PCa治疗的有效策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e41/9078851/8440c620e9d6/JO2022-7918067.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验