Chen Kang, Jiao Jianbao, Xue Jinwei, Chen Taoping, Hou Yu, Jiang Yuantao, Qian Ligang, Wang Yunfei, Ma Zheng, Liang Zhixing, Sun Bo, Ren Qiao
Department of Orthopedics, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Department of Rheumatism and Immunology, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Oncol Rep. 2020 Mar;43(3):886-896. doi: 10.3892/or.2020.7460. Epub 2020 Jan 13.
Osteosarcoma is one of the most malignant bone tumors, and its major threats are aggressive invasion and early tumor metastasis, which result in a poor prognosis and high mortality. Accumulating evidence indicates that ginsenoside compound K (CK) has a significant antitumor effect, particularly on the inhibition of proliferation and invasion of numerous human tumors. In the present study, it was revealed that CK inhibited the viability and proliferation of osteosarcoma cells. Moreover, it was demonstrated that CK induced apoptosis and inhibited the migration and invasion of osteosarcoma cells via apoptotic staining, Annexin V/PI staining, and Transwell invasion assays. Furthermore, at the molecular level, the present results confirmed that apoptosis and invasion‑related proteins were regulated by CK, which was possibly related to the blockade of the PI3K/mTOR/p70S6K1 signaling pathway. In summary, the present findings indicated that CK inhibited viability and proliferation, induced apoptosis, and inhibited the migration and invasion of osteosarcoma cells through the PI3K/mTOR/p70S6K1 signaling pathway.
骨肉瘤是最恶性的骨肿瘤之一,其主要威胁是侵袭性浸润和早期肿瘤转移,这导致预后不良和高死亡率。越来越多的证据表明,人参皂苷Compound K(CK)具有显著的抗肿瘤作用,尤其是对多种人类肿瘤增殖和浸润的抑制作用。在本研究中,发现CK抑制骨肉瘤细胞的活力和增殖。此外,通过凋亡染色、Annexin V/PI染色和Transwell侵袭试验表明,CK诱导骨肉瘤细胞凋亡并抑制其迁移和侵袭。此外,在分子水平上,本研究结果证实凋亡和侵袭相关蛋白受CK调节,这可能与PI3K/mTOR/p70S6K1信号通路的阻断有关。总之,本研究结果表明,CK通过PI3K/mTOR/p70S6K1信号通路抑制骨肉瘤细胞的活力和增殖,诱导细胞凋亡,并抑制其迁移和侵袭。