Suppr超能文献

普萘洛尔可阻断骨肉瘤细胞周期进程,抑制血管生成,并与顺铂为基础的化疗联合抑制异种移植物生长。

Propranolol blocks osteosarcoma cell cycle progression, inhibits angiogenesis and slows xenograft growth in combination with cisplatin-based chemotherapy.

机构信息

Center for Molecular and Translational Oncology (COMTra), Science and Technology Department, National University of Quilmes, Buenos Aires, Argentina.

Center for Translational Medicine, El Cruce "Néstor Kirchner" Hospital, Buenos Aires, Argentina.

出版信息

Sci Rep. 2022 Sep 8;12(1):15058. doi: 10.1038/s41598-022-18324-3.

Abstract

Osteosarcoma is still associated with limited response to standard-of-care therapy and alarmingly elevated mortality rates, especially in low- and middle-income countries. Despite multiple efforts to repurpose β-blocker propranolol in oncology, its potential application in osteosarcoma management remains largely unexplored. Considering the unsatisfied clinical needs of this aggressive disease, we evaluated the antitumoral activity of propranolol using different in vitro and in vivo osteosarcoma preclinical models, alone or in addition to chemotherapy. Propranolol significantly impaired cellular growth in β2-adrenergic receptor-expressing MG-63 and U-2OS cells, and was capable of blocking growth-stimulating effects triggered by catecholamines. siRNA-mediated ADRB2 knockdown in MG-63 cells was associated with decreased cell survival and a significant attenuation of PPN anti-osteosarcoma activity. Direct cytostatic effects of propranolol were independent of apoptosis induction and were associated with reduced mitosis, G0/G1 cell cycle arrest and a significant down-regulation of cell cycle regulator Cyclin D1. Moreover, colony formation, 3D spheroid growth, cell chemotaxis and capillary-like tube formation were drastically impaired after propranolol treatment. Interestingly, anti-migratory activity of β-blocker was associated with altered actin cytoskeleton dynamics. In vivo, propranolol treatment (10 mg/kg/day i.p.) reduced the early angiogenic response triggered by MG-63 cells in nude mice. Synergistic effects were observed in vitro after combining propranolol with chemotherapeutic agent cisplatin. Sustained administration of propranolol (10 mg/kg/day i.p., five days a week), alone and especially in addition to low-dose metronomic cisplatin (2 mg/kg/day i.p., three times a week), markedly reduced xenograft progression. After histological analysis, propranolol and cisplatin combination resulted in low tumor mitotic index and increased tumor necrosis. β-blockade using propranolol seems to be an achievable and cost-effective therapeutic approach to modulate osteosarcoma aggressiveness. Further translational studies of propranolol repurposing in osteosarcoma are warranted.

摘要

骨肉瘤患者的标准治疗反应仍然有限,死亡率高得惊人,尤其是在中低收入国家。尽管人们多次努力将β受体阻滞剂普萘洛尔重新用于肿瘤学,但它在骨肉瘤治疗中的潜在应用仍在很大程度上未被探索。鉴于这种侵袭性疾病的临床需求未得到满足,我们使用不同的骨肉瘤临床前体外和体内模型评估了普萘洛尔的抗肿瘤活性,单独使用或与化疗联合使用。普萘洛尔显著抑制了表达β2-肾上腺素能受体的 MG-63 和 U-2OS 细胞的细胞生长,并能够阻断儿茶酚胺触发的生长刺激作用。在 MG-63 细胞中,通过 siRNA 介导的 ADRB2 敲低与细胞存活率降低以及 PPN 抗骨肉瘤活性的显著减弱相关。普萘洛尔的直接细胞抑制作用与诱导细胞凋亡无关,与有丝分裂减少、G0/G1 细胞周期阻滞和细胞周期调节蛋白 Cyclin D1 的显著下调有关。此外,普萘洛尔处理后集落形成、3D 球体生长、细胞趋化和毛细血管样管形成均受到严重破坏。有趣的是,β-阻断剂的抗迁移活性与肌动蛋白细胞骨架动力学的改变有关。在体内,普萘洛尔治疗(10mg/kg/天腹腔内注射)可减少裸鼠中 MG-63 细胞引发的早期血管生成反应。体外联合化疗药物顺铂观察到协同作用。普萘洛尔(10mg/kg/天腹腔内注射,每周 5 天)持续给药,单独给药,特别是与低剂量节拍式顺铂(2mg/kg/天腹腔内注射,每周 3 次)联合给药,可显著减少异种移植物的进展。组织学分析后,普萘洛尔和顺铂联合治疗可降低肿瘤有丝分裂指数并增加肿瘤坏死。使用普萘洛尔进行β阻断似乎是一种可行且具有成本效益的治疗方法,可以调节骨肉瘤的侵袭性。普萘洛尔在骨肉瘤中的重新应用的进一步转化研究是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3df4/9458647/cf56ee9ceb73/41598_2022_18324_Fig1_HTML.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