Abe S, Kubota T, Otani Y, Furukawa T, Watanabe M, Kumai K, Akiyama T, Akinaga S, Kitajima M
Department of Surgery, School of Medicine, Keio University, Shinjuku-ku, Tokyo 160-8582, Japan.
Jpn J Cancer Res. 2001 May;92(5):537-45. doi: 10.1111/j.1349-7006.2001.tb01127.x.
Mechanisms underlying tumor sensitivity to the antitumor agent UCN-01 (7-hydroxystaurosporine) were examined in the nude mouse model using three human tumor xenografts, two pancreatic cancers (PAN-3-JCK and CRL 1420) and a breast cancer (MX-1). UCN-01 antitumor activity was evaluated in terms of relative tumor weights in treated and untreated mice bearing the tumor xenografts. The activity of cyclin-dependent kinase 2 (CDK2), levels of p21 and p27 proteins, pRb status and cell cycle were evaluated. Induction of p21 and apoptosis were also assessed immunohistochemically in CRL 1420. UCN-01 was administered intraperitoneally at a dose of either 5 or 10 mg / kg daily for 5 days followed by a further 5 injections after an interval of 2 days. UCN-01 significantly suppressed the growth of both pancreatic cancers, but was ineffective against MX-1. p21 protein expression was markedly induced in the UCN-01-sensitive pancreatic carcinoma xenografts at both doses, but p21 induction was only evident in the UCN-01-resistant MX-1 at 10 mg / kg. MX-1 exhibited CDK2 activity that was 6-fold higher than that of pancreatic cancer strains, which may explain the resistance of MX-1 to UCN-01 despite the induction of p21 at the dose of 10 mg / kg. The UCN-01-sensitive tumors exhibited G1 arrest and increased levels of apoptosis, changes not observed in resistant MX-1. In conclusion, it appears that a determining factor of in vivo UCN-01 sensitivity involves the balance of CDK2 kinase activity and p21 protein induction, resulting in augmented pRb phosphorylation, G1 cell cycle arrest and apoptosis.
利用三种人肿瘤异种移植模型,即两种胰腺癌(PAN - 3 - JCK和CRL 1420)和一种乳腺癌(MX - 1),在裸鼠模型中研究了肿瘤对抗肿瘤药物UCN - 01(7 - 羟基星孢菌素)敏感的潜在机制。根据携带肿瘤异种移植的治疗组和未治疗组小鼠的相对肿瘤重量来评估UCN - 01的抗肿瘤活性。评估了细胞周期蛋白依赖性激酶2(CDK2)的活性、p21和p27蛋白水平、pRb状态及细胞周期。还通过免疫组织化学方法在CRL 1420中评估了p21的诱导和凋亡情况。UCN - 01以每日5或10 mg / kg的剂量腹腔注射,持续5天,间隔2天后再进行5次注射。UCN - 01显著抑制了两种胰腺癌的生长,但对MX - 1无效。在两个剂量下,UCN - 01敏感的胰腺癌异种移植瘤中p21蛋白表达均明显诱导,但p21诱导仅在10 mg / kg剂量的UCN - 01耐药的MX - 1中明显。MX - 1显示出比胰腺癌株高6倍的CDK2活性,这可能解释了尽管在10 mg / kg剂量下诱导了p21,但MX - 1对UCN - 01仍具有抗性。UCN - 01敏感的肿瘤表现出G1期阻滞和凋亡水平增加,而在耐药的MX - 1中未观察到这些变化。总之,体内UCN - 01敏感性的一个决定性因素似乎涉及CDK2激酶活性和p21蛋白诱导的平衡,导致pRb磷酸化增加、G1期细胞周期阻滞和凋亡。