Department of Orthopaedic Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
Acta Med Okayama. 2024 Apr;78(2):151-161. doi: 10.18926/AMO/66924.
Soft-tissue sarcoma (STS) is a heterogeneous group of rare tumors originating predominantly from the embryonic mesoderm. Despite the development of combined modalities including radiotherapy, STSs are often refractory to antitumor modalities, and novel strategies that improve the prognosis of STS patients are needed. We previously demonstrated the therapeutic potential of two telomerase-specific replication-competent oncolytic adenoviruses, OBP-301 and tumor suppressor p53-armed OBP-702, in human STS cells. Here, we demonstrate in vitro and in vivo antitumor effects of OBP-702 in combination with ionizing radiation against human STS cells (HT1080, NMS-2, SYO-1). OBP-702 synergistically promoted the antitumor effect of ionizing radiation in the STS cells by suppressing the expression of B-cell lymphoma-X large (BCL-xL) and enhancing ionizing radiation-induced apoptosis. The in vivo experiments demonstrated that this combination therapy significantly suppressed STS tumors' growth. Our results suggest that OBP-702 is a promising antitumor reagent for promoting the radiosensitivity of STS tumors.
软组织肉瘤 (STS) 是一组源自胚胎中胚层的罕见肿瘤,具有异质性。尽管采用了包括放疗在内的联合治疗方法,但 STS 通常对抗肿瘤方法具有耐药性,因此需要新的策略来改善 STS 患者的预后。我们之前证明了两种端粒酶特异性复制型溶瘤腺病毒 OBP-301 和肿瘤抑制因子 p53 武装的 OBP-702 在人 STS 细胞中的治疗潜力。在这里,我们证明了 OBP-702 与电离辐射联合用于人类 STS 细胞(HT1080、NMS-2、SYO-1)的体外和体内抗肿瘤作用。OBP-702 通过抑制 B 细胞淋巴瘤-X 大 (BCL-xL) 的表达和增强电离辐射诱导的细胞凋亡,协同促进 STS 细胞的抗肿瘤作用。体内实验表明,这种联合治疗显著抑制了 STS 肿瘤的生长。我们的结果表明,OBP-702 是一种有前途的抗肿瘤试剂,可促进 STS 肿瘤的放射敏感性。