Manfredi Mark G, Ecsedy Jeffrey A, Meetze Kristan A, Balani Suresh K, Burenkova Olga, Chen Wei, Galvin Katherine M, Hoar Kara M, Huck Jessica J, LeRoy Patrick J, Ray Emily T, Sells Todd B, Stringer Bradley, Stroud Stephen G, Vos Tricia J, Weatherhead Gabriel S, Wysong Deborah R, Zhang Mengkun, Bolen Joseph B, Claiborne Christopher F
Department of Oncology, Millennium Pharmaceuticals Inc., 40 Landsdowne Street, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):4106-11. doi: 10.1073/pnas.0608798104. Epub 2007 Feb 23.
Increased Aurora A expression occurs in a variety of human cancers and induces chromosomal abnormalities during mitosis associated with tumor initiation and progression. MLN8054 is a selective small-molecule Aurora A kinase inhibitor that has entered Phase I clinical trials for advanced solid tumors. MLN8054 inhibits recombinant Aurora A kinase activity in vitro and is selective for Aurora A over the family member Aurora B in cultured cells. MLN8054 treatment results in G(2)/M accumulation and spindle defects and inhibits proliferation in multiple cultured human tumor cells lines. Growth of human tumor xenografts in nude mice was dramatically inhibited after oral administration of MLN8054 at well tolerated doses. Moreover, the tumor growth inhibition was sustained after discontinuing MLN8054 treatment. In human tumor xenografts, MLN8054 induced mitotic accumulation and apoptosis, phenotypes consistent with inhibition of Aurora A. MLN8054 is a selective inhibitor of Aurora A kinase that robustly inhibits growth of human tumor xenografts and represents an attractive modality for therapeutic intervention of human cancers.
Aurora A表达增加出现在多种人类癌症中,并在有丝分裂期间诱发与肿瘤起始和进展相关的染色体异常。MLN8054是一种选择性小分子Aurora A激酶抑制剂,已进入晚期实体瘤的I期临床试验。MLN8054在体外抑制重组Aurora A激酶活性,并且在培养细胞中对Aurora A的选择性高于家族成员Aurora B。MLN8054处理导致G(2)/M期积累和纺锤体缺陷,并抑制多种培养的人类肿瘤细胞系的增殖。以耐受性良好的剂量口服MLN8054后,裸鼠体内人肿瘤异种移植物的生长受到显著抑制。此外,在停止MLN8054处理后,肿瘤生长抑制仍持续存在。在人肿瘤异种移植物中,MLN8054诱导有丝分裂积累和凋亡,这些表型与抑制Aurora A一致。MLN8054是一种Aurora A激酶的选择性抑制剂,能有力地抑制人肿瘤异种移植物的生长,是人类癌症治疗干预的一种有吸引力的方式。