Hanauske Axel-Rainer, Oberschmidt Olaf, Hanauske-Abel Hartmut, Lahn Michael M, Eismann Ulrike
Asklepios Klinik St. Georg, Lohmühlenstr. 5, 20099, Hamburg, Germany.
Invest New Drugs. 2007 Jun;25(3):205-10. doi: 10.1007/s10637-007-9038-7. Epub 2007 Mar 9.
Enzastaurin (LY317615.HCl) is an antiproliferative agent targeted specifically against PKC-beta. We have investigated the antitumoral effects of Enzastaurin against human cancer cell lines and freshly explanted human tumor tissue. Ten human cancer cell lines (NSCLC, colon, and thyroid) and human tumor specimens from 72 patients were used for in vitro studies in a cloning assay (HTCA). Cell lines and primary tumor cells were exposed to Enzastaurin for either 1 h or 7 days, or for 1 h or 21 days. At clinically achievable concentrations of Enzastaurin, inhibition of cell growth was observed for lung, colorectal, and thyroid cancer cell lines in a concentration dependent manner. Patient specimens exposed 1 h or 21 days to 1,400 nM Enzastaurin demonstrated inhibition rates of 24 and 32%, respectively. Marked inhibitory effects were observed in breast, thyroid, head/neck, non-small cell lung cancer, pancreatic cancer, and melanoma. In addition to its established antiangiogenic effects, Enzastaurin has direct antitumor activity against established human cancer cell lines and primary tumor specimens. This warrants further clinical development in tumors which have been identified to be potentially sensitive to Enzastaurin.
恩杂鲁胺(LY317615.HCl)是一种专门针对蛋白激酶C-β的抗增殖剂。我们研究了恩杂鲁胺对人癌细胞系和新鲜移植的人肿瘤组织的抗肿瘤作用。十种人癌细胞系(非小细胞肺癌、结肠癌和甲状腺癌)以及来自72名患者的人肿瘤标本用于克隆分析(HTCA)的体外研究。细胞系和原发性肿瘤细胞分别暴露于恩杂鲁胺1小时或7天,或1小时或21天。在恩杂鲁胺临床可达到的浓度下,观察到肺癌、结肠癌细胞系和甲状腺癌细胞系的细胞生长受到浓度依赖性抑制。暴露于1400 nM恩杂鲁胺1小时或21天的患者标本的抑制率分别为24%和32%。在乳腺癌、甲状腺癌、头颈部癌、非小细胞肺癌、胰腺癌和黑色素瘤中观察到明显的抑制作用。除了已确定的抗血管生成作用外,恩杂鲁胺对已建立的人癌细胞系和原发性肿瘤标本具有直接抗肿瘤活性。这使得在已确定对恩杂鲁胺潜在敏感的肿瘤中进行进一步的临床开发成为必要。