Sano Daisuke, Matsuda Hideki, Ishiguro Yukari, Nishimura Goshi, Kawakami Mariko, Tsukuda Mamoru
Department of Biology and Function in the Head and Neck, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Yokohama 236-0004, Japan.
Oncol Rep. 2006 Feb;15(2):329-34.
Taxanes, a new class of antitumor drugs, are effective against a large number of human tumors, although there are problems with drug resistance. The novel taxane, IDN5109, is characterized by its high tolerability, antitumor efficacy, ability to overcome multidrug resistance, and oral bioavailabilty. We investigated the cellular response of IDN5109 to head and neck squamous cell carcinoma (HNSCC), and compared the antitumor activity of IDN5109 with that of paclitaxel. This is the first demonstration of antitumor effects of IDN5109 on HNSCC. In in vitro experiments, IDN5109 showed antiproliferative effects against HNSCC cell lines. After treatment with IDN5109, Bcl-2 and Bcl-XL were down-regulated, Bax was up-regulated, and caspase-3 was activated. After treatment with IDN5109, concentrations of both VEGF and IL-8 in the culture supernatant of HNSCC cells decreased. In in vivo experiments, the oral administration of IDN5109 showed antitumor effects against HNSCC tumor xenografts. Immunohistochemistry showed that IDN5109 inhibited tumor angiogenesis and induced apoptosis in HNSCC cells, producing a decreased blood vessel density and increased apoptosis index. On the basis of these results, IDN5109 is useful as a chemotherapeutic agent against HNSCC.
紫杉烷类是一类新型抗肿瘤药物,对多种人类肿瘤有效,尽管存在耐药性问题。新型紫杉烷IDN5109具有高耐受性、抗肿瘤疗效、克服多药耐药的能力以及口服生物利用度等特点。我们研究了IDN5109对头颈部鳞状细胞癌(HNSCC)的细胞反应,并将IDN5109与紫杉醇的抗肿瘤活性进行了比较。这是首次证明IDN5109对HNSCC具有抗肿瘤作用。在体外实验中,IDN5109对HNSCC细胞系显示出抗增殖作用。用IDN5109处理后,Bcl-2和Bcl-XL下调,Bax上调,caspase-3被激活。用IDN5109处理后,HNSCC细胞培养上清液中VEGF和IL-8的浓度均降低。在体内实验中,口服IDN5109对HNSCC肿瘤异种移植显示出抗肿瘤作用。免疫组织化学显示,IDN5109抑制HNSCC细胞中的肿瘤血管生成并诱导凋亡,导致血管密度降低和凋亡指数增加。基于这些结果,IDN5109可作为治疗HNSCC的化疗药物。