Szende Béla, Okada Yoshio, Tsuda Yuko, Horvath Aniko, Bökönyi Gyöngyi, Okamoto Shosuke, Wanaka Keiko, Kéri György
1st Institute of Pathology and Experimental Cancer Research, Semmelweis University, Molecular Pathology Research Group of Hungarian Academy of Sciences, Budapest, Hungary.
In Vivo. 2002 Sep-Oct;16(5):281-6.
The novel plasmin inhibitor YO-2, which also exerts an apoptosis-inducing effect on various human tumor cell cultures, was examined regarding its tumor growth inhibitory and antimetastatic action. The tumor growth inhibitory effect of YO-2 was studied using HT-29 human colon carcinoma, HT-18 human melanoma and HT-58 human B cell lymphoma inoculated as xenografts into immuno-deprived mice. Antimetastatic activity was tested on the B16 mouse melanoma muscle-lung model. YO-2 inhibited the growth of all xenografts in the range of 40-50%, when administered s.c. at a dose of 2.0 mg/kg (HT-29, HT-58) or orally at a dose of 0.4 mg/kg (HT-18). YO-2 decreased the number of lung metastasis found in mice inoculated i.m. with B16 melanoma, 4 mg/kg being the most effective. Since YO-2 is the only plasmin inhibitor having antihemorrhagic and also antitumor effect, this compound could be rationally used in combination therapy of neoplastic disease, especially when hemorrhage aggravates the course of the disease.
新型纤溶酶抑制剂YO-2对多种人类肿瘤细胞培养物也具有诱导凋亡的作用,本研究检测了其对肿瘤生长的抑制作用和抗转移作用。采用将HT-29人结肠癌、HT-18人黑色素瘤和HT-58人B细胞淋巴瘤接种为异种移植物至免疫缺陷小鼠体内的方法,研究YO-2的肿瘤生长抑制作用。在B16小鼠黑色素瘤肌肉-肺转移模型上测试其抗转移活性。当以2.0mg/kg的剂量皮下给药(HT-29、HT-58)或以0.4mg/kg的剂量口服给药(HT-18)时,YO-2抑制所有异种移植物的生长,抑制率在40%-50%之间。YO-2减少了经肌肉注射接种B16黑色素瘤的小鼠肺部转移灶的数量,4mg/kg为最有效剂量。由于YO-2是唯一具有抗出血和抗肿瘤作用的纤溶酶抑制剂,该化合物可合理用于肿瘤疾病的联合治疗,尤其是在出血使疾病进程加重时。