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佩利福新诱导骨肉瘤细胞凋亡:骨肉瘤治疗的新启示?

Perifosine induces cell apoptosis in human osteosarcoma cells: new implication for osteosarcoma therapy?

机构信息

Department of Orthopedics, BenQ Medical Center, Nanjing Medical University, Nanjing, Jiangsu, China.

出版信息

Cell Biochem Biophys. 2013 Mar;65(2):217-27. doi: 10.1007/s12013-012-9423-5.

Abstract

Despite the advances of adjuvant chemotherapy and significant improvement of survival, the prognosis for patients with osteosarcoma is generally poor. The search for more effective anti-osteosarcoma agents is necessary and urgent. Here we report that perifosine induces cell apoptosis and growth inhibition in cultured human osteosarcoma cells. Perifosine blocks Akt/mTOR complex 1 (mTORC1) signaling, while promoting caspase-3, c-Jun N-terminal kinases (JNK), and p53 activation. Further, perifosine inhibits survivin expression probably by disrupting its association with heat shock protein-90 (HSP-90). These signaling changes together were responsible for a marked increase of osteosarcoma cell apoptosis and growth inhibition. Finally, we found that a low dose of perifosine enhanced etoposide- or doxorubicin-induced anti-OS cells activity. The results together suggest that perifosine might be used as a novel and effective anti-osteosarcoma agent.

摘要

尽管辅助化疗取得了进展,生存时间显著改善,但骨肉瘤患者的预后通常仍较差。因此,有必要寻找更有效的抗骨肉瘤药物。本文报道了帕非司亭能诱导人骨肉瘤细胞凋亡和生长抑制。帕非司亭能阻断 Akt/mTOR 复合物 1(mTORC1)信号,同时促进半胱天冬酶-3、c-Jun N 端激酶(JNK)和 p53 的激活。此外,帕非司亭可能通过破坏其与热休克蛋白 90(HSP-90)的结合来抑制生存素的表达。这些信号变化共同导致骨肉瘤细胞凋亡和生长抑制的显著增加。最后,我们发现低剂量帕非司亭能增强依托泊苷或阿霉素对 OS 细胞的杀伤作用。这些结果表明,帕非司亭可能作为一种新型有效的抗骨肉瘤药物。

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