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骨肉瘤和软组织肉瘤:端粒酶特异性溶瘤病毒疗法的新靶点。

Bone and Soft-Tissue Sarcoma: A New Target for Telomerase-Specific Oncolytic Virotherapy.

作者信息

Tazawa Hiroshi, Hasei Joe, Yano Shuya, Kagawa Shunsuke, Ozaki Toshifumi, Fujiwara Toshiyoshi

机构信息

Center for Innovative Clinical Medicine, Okayama University Hospital, Okayama 700-8558, Japan.

Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan.

出版信息

Cancers (Basel). 2020 Feb 18;12(2):478. doi: 10.3390/cancers12020478.

Abstract

Adenovirus serotype 5 (Ad5) is widely and frequently used as a virus vector in cancer gene therapy and oncolytic virotherapy. Oncolytic virotherapy is a novel antitumor treatment for inducing lytic cell death in tumor cells without affecting normal cells. Based on the Ad5 genome, we have generated three types of telomerase-specific replication-competent oncolytic adenoviruses: OBP-301 (Telomelysin), green fluorescent protein (GFP)-expressing OBP-401 (TelomeScan), and tumor suppressor -armed OBP-702. These viruses drive the expression of the adenoviral and genes under the control of the (human telomerase reverse transcriptase-encoding gene) promoter, providing tumor-specific virus replication. This review focuses on the therapeutic potential of three promoter-driven oncolytic adenoviruses against bone and soft-tissue sarcoma cells with telomerase activity. OBP-301 induces the antitumor effect in monotherapy or combination therapy with chemotherapeutic drugs via induction of autophagy and apoptosis. OBP-401 enables visualization of sarcoma cells within normal tissues by serving as a tumor-specific labeling reagent for fluorescence-guided surgery via induction of GFP expression. OBP-702 exhibits a profound antitumor effect in OBP-301-resistant sarcoma cells via activation of the p53 signaling pathway. Taken together, telomerase-specific oncolytic adenoviruses are promising antitumor reagents that are expected to provide novel therapeutic options for the treatment of bone and soft-tissue sarcomas.

摘要

5型腺病毒(Ad5)在癌症基因治疗和溶瘤病毒疗法中被广泛且频繁地用作病毒载体。溶瘤病毒疗法是一种新型抗肿瘤治疗方法,可诱导肿瘤细胞发生溶解性细胞死亡而不影响正常细胞。基于Ad5基因组,我们构建了三种类型的端粒酶特异性复制型溶瘤腺病毒:OBP - 301(Telomelysin)、表达绿色荧光蛋白(GFP)的OBP - 401(TelomeScan)和携带肿瘤抑制因子的OBP - 702。这些病毒在人端粒酶逆转录酶编码基因(hTERT)启动子的控制下驱动腺病毒E1A和E1B基因的表达,实现肿瘤特异性病毒复制。本综述重点关注三种hTERT启动子驱动的溶瘤腺病毒对具有端粒酶活性的骨肉瘤和软组织肉瘤细胞的治疗潜力。OBP - 301通过诱导自噬和凋亡在单药治疗或与化疗药物联合治疗中发挥抗肿瘤作用。OBP - 401通过诱导GFP表达,作为荧光引导手术的肿瘤特异性标记试剂,可实现正常组织内肉瘤细胞的可视化。OBP - 702通过激活p53信号通路,对OBP - 301耐药的肉瘤细胞具有显著的抗肿瘤作用。综上所述,端粒酶特异性溶瘤腺病毒是有前景的抗肿瘤试剂,有望为骨肉瘤和软组织肉瘤的治疗提供新的治疗选择。

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