LoRusso P, Demchik L, Dan M, Polin L, Gross J L, Corbett T H
Division of Hematology/Oncology, Wayne State University, Detroit, MI 48201, USA.
Invest New Drugs. 1995;13(3):195-203. doi: 10.1007/BF00873800.
DMP 840 is a compound from a class of bis-naphthalimide antitumor agents that recently completed Phase I clinical trials at three North American centers and is currently undergoing Phase II testing. Preclinically, it was shown to have curative activity against a variety of human tumor xenograft models.
To test DMP 840 both in vitro and in vivo for antiproliferative activity against predominantly mouse tumor models.
A disk diffusion soft agar colony formation assay was used to determine the in vitro growth inhibitory activity against a selection of mouse and human tumor cell lines, and the comparable selective mouse solid tumors were used for in vivo testing.
In vitro DMP 840 exhibited equal cytotoxicity for human tumors (including MX-1 directly cultured from nude mice), mouse tumors and normal cells. In vivo DMP 840 was only modestly active or inactive against the following mouse tumors: Mam 16/C, T/C = 30% (T/C = Percent Tumor Growth Inhibition); Mam 16/C/ADR, T/C = 33%; Colon 38, T/C = 9%; Panc 03, T/C = 53%; Colon 51/A, T/C = 28%; Panc 02, T/C = 52%; P388/0, 36% ILS (Percent Increased Life Span) and P388/ADR, 14% ILS. Furthermore, the antitumor activity was only observed at the highest non-toxic dose and was associated with a large body weight loss. In contrast, the agent was highly active against the human breast tumor MX-1 implanted subcutaneously in either athymic nude or SCID mice (Nudes: T/C = 0%; 1/5 cures; SCIDS: T/C = 0%; 5/5 cures).
Although there was no selective cytotoxicity in our clonogenic assay for human versus mouse tumor cell lines, selective activity in vivo for human xenograft tumors was noted. Overall, this compound is rather unique in its differential degree of in vivo activity for human versus mouse tumors.
Phase II trials, which are ongoing, will help determine if the preclinical in vivo selective activity of DMP 840 translates to clinical activity in man.
DMP 840是一类双萘酰亚胺抗肿瘤药物中的一种化合物,该药物最近在北美三个中心完成了I期临床试验,目前正在进行II期试验。临床前研究表明,它对多种人类肿瘤异种移植模型具有治疗活性。
在体外和体内测试DMP 840对主要是小鼠肿瘤模型的抗增殖活性。
采用纸片扩散软琼脂集落形成试验来测定对一系列小鼠和人类肿瘤细胞系的体外生长抑制活性,并使用可比的选择性小鼠实体瘤进行体内试验。
在体外,DMP 840对人类肿瘤(包括直接从裸鼠培养的MX-1)、小鼠肿瘤和正常细胞表现出同等的细胞毒性。在体内,DMP 840对以下小鼠肿瘤仅表现出适度活性或无活性:Mam 16/C,T/C = 30%(T/C = 肿瘤生长抑制百分比);Mam 16/C/ADR,T/C = 33%;Colon 38,T/C = 9%;Panc 03,T/C = 53%;Colon 51/A,T/C = 28%;Panc 02,T/C = 52%;P388/0,36%ILS(寿命延长百分比)和P388/ADR,14%ILS。此外,抗肿瘤活性仅在最高无毒剂量下观察到,并且与体重大幅减轻有关。相比之下,该药物对皮下植入无胸腺裸鼠或SCID小鼠的人类乳腺肿瘤MX-1具有高度活性(裸鼠:T/C = 0%;5只中有1只治愈;SCID小鼠:T/C = 0%;5只全部治愈)。
尽管在我们针对人类与小鼠肿瘤细胞系的克隆形成试验中没有选择性细胞毒性,但在体内对人类异种移植肿瘤观察到了选择性活性。总体而言,该化合物在人类与小鼠肿瘤的体内活性差异程度方面相当独特。
正在进行的II期试验将有助于确定DMP 840临床前的体内选择性活性是否转化为人类的临床活性。