Dipartimento di Scienze della Vita, Seconda Università di Napoli, Via Vivaldi 43, I-81100 Caserta, Italy.
Biochimie. 2012 Sep;94(9):1990-6. doi: 10.1016/j.biochi.2012.05.022. Epub 2012 May 29.
Both ribosome-inactivating proteins (RIPs) and plant proteinase inhibitors, belong to protein families known to regulate cellular homeostasis and likely involved in plant defense. Nevertheless the interest in these protein classes is due to their potential use for the treatment of several important human diseases such as cancer. Thus, in the present study, type 1 ribosome-inactivating protein and wheat subtilisin/chymotrypsin inhibitor, were engineered into a chimeric protein with cytotoxic action selective for murine tumor cells, while lacking any appreciable toxicity on murine normal cells. This chimeric protein selectively sensitizes to apoptotic death cells derived from Simian-virus-40-transformed mouse fibroblasts (SVT2 cells). The cytotoxicity of this new recombinant product has been detected also on three different human malignant cells. Therefore action on tumor cells of this protein could represent a potentially very attractive novel tool for anticancer drug design.
核糖体失活蛋白(RIPs)和植物蛋白酶抑制剂都属于已知能调节细胞内稳态并可能参与植物防御的蛋白质家族。然而,人们对这些蛋白质类别的兴趣源于它们在治疗多种重要人类疾病(如癌症)方面的潜在用途。因此,在本研究中,将 1 型核糖体失活蛋白和小麦枯草溶菌素/胰凝乳蛋白酶抑制剂设计成一种具有细胞毒性的嵌合蛋白,对鼠肿瘤细胞具有选择性,但对鼠正常细胞几乎没有任何毒性。这种嵌合蛋白选择性地使源自猴病毒 40 转化的鼠成纤维细胞(SVT2 细胞)的凋亡死亡细胞敏感。该新型重组产物的细胞毒性也已在三种不同的人类恶性细胞上检测到。因此,这种蛋白对肿瘤细胞的作用可能代表一种用于抗癌药物设计的极具吸引力的新工具。