Russell-Jones Gregory, McTavish Kirsten, McEwan John, Rice John, Nowotnik David
Access Pharmaceuticals Australia Pty Ltd., Targeted Delivery, Unit 5, 15-17 Gibbes St, Chatswood, NSW, Sydney 2067, Australia.
J Inorg Biochem. 2004 Oct;98(10):1625-33. doi: 10.1016/j.jinorgbio.2004.07.009.
Targeted chemotherapy for cancer treatment offers a great potential advantage in tumour treatment due to greater specificity of delivery which leads to increased dose of the cytotoxin delivered to the tumour relative to the rest of the body. In order to achieve such selective targeted delivery one needs to identify generic markers that are over-expressed on the surface of tumour cells but are not over-expressed on normal tissue. Work of several authors has shown that some cells, such as those of rapidly dividing, aggressive tumours, over-express surface receptors involved in the uptake of vitamin B(12) [B. Rachmilewitz, M. Rachmilewitz, B. Moshkowitz, J. Gross, J. Lab. Clin. Med. 78 (1971) 275-279; B. Rachmilewitz, A. Sulkes, M. Rachmilewitz, A. Fuks, Israel J. Med. Sci. 17 (1981) 874-879] or folate [P. Garin-Chesa, I. Campbell, P.E. Saigo, J.L. Lewis Jr., L.J. Old, W.J. Rettig, Am. J. Pathol. 142 (1993) 557-567; O.C. Boerman, C.C. van Niekerk, K. Makkink, T.G.J.M. Hanselaar, P. Kenemans, L.G. Poels, Int. J. Gynecol. Pathol. 10 (1991) 15-25; G. Toffoli, C. Cernigoi, A. Russo, A. Gallo, M. Bagnoli, M. Boiocchi, Int. J. Cancer 74 (1997) 193-194; J.A. Reddy, D. Dean, M.D. Kennedy, P.S. Low, J. Pharm. Sci. 88 (1999) 1112-1118; J.A. Reddy, P.S. Low, Crit. Rev. Ther. Drug Carrier Syst. 15 (1998) 587-627; G.J. Russell-Jones, K. McTavish, J.F. McEwan, in: Proceedings of the 2nd International Symposium on Tumor Targeted Delivery Systems, 2002]. Furthermore the degree of over-expression has been found to correlate with the stage of tumour growth, with the highest levels found on stage IV carcinomas. Using fluorescently-labelled polymers to which are linked the targeting agents, vitamin B(12), folate or biotin, the relative uptake of these polymers into various types of tumour cell lines grown both in vitro and in vivo has been examined. These studies have shown that while some tumour types do NOT over-express receptors involved in vitamin uptake, most tumour types over-express receptors for folate, or vitamin B(12). In either case there is also a greatly increased expression of a yet to be identified biotin receptor. In cases of receptor over-expression, binding of the targeted fluorochrome leads to rapid internalization of these molecules within the cells to levels that are two to thirty times higher than with non-targeted polymers. Using a number of cancer models, these studies were extended further and it was found that the increased expression of receptors also leads to increased levels of killing with targeted cytotoxins. Thus the preliminary data described suggests that the use of vitamins as targeting agents has enormous potential for use in cancer diagnosis and chemotherapy.
由于给药的特异性更高,相对于身体其他部位,靶向化疗在癌症治疗中能够将更多剂量的细胞毒素递送至肿瘤,因此在肿瘤治疗中具有巨大的潜在优势。为了实现这种选择性靶向递送,需要识别在肿瘤细胞表面过度表达但在正常组织中不表达的通用标志物。几位作者的研究表明,一些细胞,如快速分裂、侵袭性肿瘤的细胞,会过度表达参与摄取维生素B12的表面受体[B. Rachmilewitz, M. Rachmilewitz, B. Moshkowitz, J. Gross, J. Lab. Clin. Med. 78 (1971) 275 - 279; B. Rachmilewitz, A. Sulkes, M. Rachmilewitz, A. Fuks, Israel J. Med. Sci. 17 (1981) 874 - 879]或叶酸[P. Garin - Chesa, I. Campbell, P.E. Saigo, J.L. Lewis Jr., L.J. Old, W.J. Rettig, Am. J. Pathol. 142 (1993) 557 - 567; O.C. Boerman, C.C. van Niekerk, K. Makkink, T.G.J.M. Hanselaar, P. Kenemans, L.G. Poels, Int. J. Gynecol. Pathol. 10 (1991) 15 - 25; G. Toffoli, C. Cernigoi, A. Russo, A. Gallo, M. Bagnoli, M. Boiocchi, Int. J. Cancer 74 (1997) 193 - 194; J.A. Reddy, D. Dean, M.D. Kennedy, P.S. Low, J. Pharm. Sci. 88 (1999) 1112 - 1118; J.A. Reddy, P.S. Low, Crit. Rev. Ther. Drug Carrier Syst. 15 (1998) 587 - 627; G.J. Russell - Jones, K. McTavish, J.F. McEwan, in: Proceedings of the 2nd International Symposium on Tumor Targeted Delivery Systems, 2002]。此外,发现过度表达的程度与肿瘤生长阶段相关,在IV期癌中发现的水平最高。使用连接了靶向剂维生素B12、叶酸或生物素的荧光标记聚合物,研究了这些聚合物在体外和体内培养的各种类型肿瘤细胞系中的相对摄取情况。这些研究表明,虽然某些肿瘤类型不过度表达参与维生素摄取的受体,但大多数肿瘤类型会过度表达叶酸或维生素B12的受体。在这两种情况下,尚未鉴定的生物素受体的表达也大大增加。在受体过度表达的情况下,靶向荧光染料的结合会导致这些分子在细胞内迅速内化,其水平比非靶向聚合物高出两到三十倍。使用多种癌症模型,这些研究进一步扩展,发现受体表达的增加也会导致靶向细胞毒素的杀伤水平提高。因此,所述初步数据表明,使用维生素作为靶向剂在癌症诊断和化疗中具有巨大的应用潜力。