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ZD6474,一种小分子酪氨酸激酶抑制剂,增强了辐射对人鼻咽癌的抗肿瘤和抗转移作用。

ZD6474, a small molecule tyrosine kinase inhibitor, potentiates the anti-tumor and anti-metastasis effects of radiation for human nasopharyngeal carcinoma.

机构信息

State Key Laboratory of Oncology in South China, Cancer Center, Sun Yat-Sen University, Guangzhou, 510060, PR China.

出版信息

Curr Cancer Drug Targets. 2010 Sep;10(6):611-22. doi: 10.2174/156800910791859506.

Abstract

PURPOSE

To investigate the capacity for ZD6474, a small molecule tyrosine kinase inhibitor, to enhance anti-tumor and anti-metastasis effects of radiation on human nasopharyngeal carcinoma (NPC).

EXPERIMENTAL DESIGN

NPC cell lines and xenograft models were evaluated following treatment with ZD6474 and radiation alone and in combination compared with untreated control mice.

RESULTS

Treatment with ZD6474 enhanced the anti-proliferative effect of radiation on NPC cell lines as detected by cell proliferation and apoptosis assays. ZD6474 also induced a significant increase in the radiosensitivity of NPC cells, with radiation enhancement ratios (RERs) ranging from 1.2 to 1.6. Despite the cytotoxicity exhibited by NPC cells following radiotherapy, the invasion and migration of NPC cells was found to be unaffected. In contrast, treatment with ZD6474 strongly inhibited the invasion and migration of NPC cells. When the administration of radiation and ZD6474 was investigated in vitro, the ability of ZD6474 to inhibit activation of the pro-survival signaling pathways induced by radiation was demonstrated. In vivo, ZD6474 significantly enhanced the anti-metastasis effects of radiation, while treatment with radiation and ZD6474 was found to be well tolerated and resulted in a strong inhibition of tumor growth.

CONCLUSIONS

Our results suggest the combination of radiation and ZD6474 represents a promising strategy for the treatment of human NPC.

摘要

目的

研究小分子酪氨酸激酶抑制剂 ZD6474 增强放射治疗对人鼻咽癌(NPC)的抗肿瘤和抗转移作用的能力。

实验设计

单独和联合使用 ZD6474 和放射治疗以及未治疗的对照小鼠,评估 NPC 细胞系和异种移植模型。

结果

ZD6474 处理增强了 NPC 细胞系的放射增殖抑制作用,通过细胞增殖和凋亡测定检测。ZD6474 还诱导 NPC 细胞对放射的敏感性显著增加,放射增强比(RER)范围为 1.2 至 1.6。尽管 NPC 细胞在放射治疗后表现出细胞毒性,但 NPC 细胞的侵袭和迁移不受影响。相比之下,ZD6474 处理强烈抑制 NPC 细胞的侵袭和迁移。当研究体外放射治疗和 ZD6474 的给药时,证明了 ZD6474 抑制由放射诱导的生存信号通路激活的能力。在体内,ZD6474 显著增强了放射的抗转移作用,而放射和 ZD6474 的联合治疗耐受性良好,导致肿瘤生长受到强烈抑制。

结论

我们的结果表明,放射治疗联合 ZD6474 可能是治疗人类 NPC 的一种很有前途的策略。

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