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Rho 激酶抑制剂可阻断黑素瘤细胞迁移并抑制转移。

Rho kinase inhibitors block melanoma cell migration and inhibit metastasis.

机构信息

Division of Cancer Biology, Institute of Cancer Research, London, United Kingdom.

Cancer Research UK Cancer Therapeutics Unit, Division of Cancer Therapeutics, Institute of Cancer Research, Sutton, Surrey, United Kingdom.

出版信息

Cancer Res. 2015 Jun 1;75(11):2272-84. doi: 10.1158/0008-5472.CAN-14-2156. Epub 2015 Apr 3.

DOI:10.1158/0008-5472.CAN-14-2156
PMID:25840982
Abstract

There is an urgent need to identify new therapeutic opportunities for metastatic melanoma. Fragment-based screening has led to the discovery of orally available, ATP-competitive AKT kinase inhibitors, AT13148 and CCT129254. These compounds also inhibit the Rho-kinases ROCK 1 and ROCK 2 and we show they potently inhibit ROCK activity in melanoma cells in culture and in vivo. Treatment of melanoma cells with CCT129254 or AT13148 dramatically reduces cell invasion, impairing both "amoeboid-like" and mesenchymal-like modes of invasion in culture. Intravital imaging shows that CCT129254 or AT13148 treatment reduces the motility of melanoma cells in vivo. CCT129254 inhibits melanoma metastasis when administered 2 days after orthotopic intradermal injection of the cells, or when treatment starts after metastases have arisen. Mechanistically, our data suggest that inhibition of ROCK reduces the ability of melanoma cells to efficiently colonize the lungs. These results suggest that these novel inhibitors of ROCK may be beneficial in the treatment of metastasis.

摘要

目前迫切需要为转移性黑色素瘤找到新的治疗机会。基于片段的筛选导致了可口服的、ATP 竞争性的 AKT 激酶抑制剂 AT13148 和 CCT129254 的发现。这些化合物还抑制 Rho 激酶 ROCK1 和 ROCK2,我们证明它们在培养物和体内强烈抑制黑色素瘤细胞中的 ROCK 活性。用 CCT129254 或 AT13148 处理黑色素瘤细胞可显著降低细胞侵袭,损害培养物中“阿米巴样”和间充质样侵袭模式。活体成像显示,CCT129254 或 AT13148 治疗可降低体内黑色素瘤细胞的迁移能力。在原位真皮内注射细胞后 2 天给予 CCT129254 或在转移发生后开始治疗时,CCT129254 可抑制黑色素瘤转移。从机制上讲,我们的数据表明,抑制 ROCK 降低了黑色素瘤细胞有效定植肺部的能力。这些结果表明,这些新型 ROCK 抑制剂可能有益于治疗转移。

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