Institute of Translational Pharmacology, National Research Council of Italy, Rome, Italy.
Curr Cancer Drug Targets. 2011 Jun;11(5):572-85. doi: 10.2174/156800911795655976.
An innovative approach for cancer therapy implies the use of drugs covalently conjugated to macromolecular carriers that specifically target molecules over-expressed on tumor cells. This drug delivery strategy may allow a controlled release of the drug and a high targeting selectivity on tumor cells, increasing drug cytotoxicity and decreasing its undesirable side effects. We provide in vitro and in vivo preclinical data on the antitumor efficacy of ONCOFID™-S, a new bioconjugate of hyaluronic acid (HA) with SN-38 (the CPT11 active metabolite), that support the validity of the drug delivery strategy implying the use of HA as macromolecular carrier of antineoplastic drugs, an approach based on the over-expression of its target CD44 (the receptor for HA-mediated motility) in a wide variety of cancers. We show that ONCOFID™-S exerts a strong in vitro anti-proliferative activity on CD44 over-expressing rat DHD/K12/trb colon adenocarcinoma cells, as well as on gastric, breast, oesophageal, ovarian and lung human cancer cells, higher than that exerted by unconjugated SN-38. We also demonstrated the in vivo anti-tumor efficacy of locoregional treatment with ONCOFID™-S on two pre-clinical models of colorectal cancer (CRC) in BDIX rats: a) syngeneic model of subcutaneous tumor; b) syngeneic model of metastatic tumor induced by injection of cells into the peritoneal cavity, mimicking the clinical situation of peritoneal carcinomatosis. Specifically, in the latter model ONCOFID™-S is able to dramatically reduce all parameters indicative of a poor prognosis in peritoneal metastatization of CRC without any myelotoxicity or mesothelial inflammation. We propose this CD44-targeted therapeutic strategy for locoregional treatment of peritoneal carcinomatosis from CRC, against which systemic chemotherapy results almost inefficient.
一种癌症治疗的创新方法涉及将药物共价连接到对肿瘤细胞上过表达的分子具有特异性靶向的大分子载体上。这种药物递送策略可以允许药物的控制释放和对肿瘤细胞的高靶向选择性,从而增加药物的细胞毒性并降低其不良副作用。我们提供了 ONCOFID™-S 的体外和体内临床前数据,ONCOFID™-S 是透明质酸(HA)与 SN-38(CPT11 活性代谢物)的新生物缀合物,支持使用 HA 作为抗肿瘤药物的大分子载体的药物递送策略的有效性,这种方法基于其靶标 CD44(透明质酸介导的运动的受体)在多种癌症中的过表达。我们表明,ONCOFID™-S 在体外对 CD44 过表达的大鼠 DHD/K12/trb 结肠腺癌细胞以及胃、乳腺、食管、卵巢和肺人类癌细胞具有很强的抗增殖活性,高于未缀合的 SN-38。我们还证明了 ONCOFID™-S 在 BDIX 大鼠两种结直肠癌(CRC)的局部治疗中的体内抗肿瘤功效:a)皮下肿瘤的同基因模型;b)通过注射细胞到腹腔中诱导的转移性肿瘤的同基因模型,模拟腹膜癌病的临床情况。具体而言,在后一种模型中,ONCOFID™-S 能够显著降低 CRC 腹膜转移中所有预示预后不良的参数,而没有任何骨髓毒性或间皮炎症。我们提出了针对 CRC 腹膜癌病的局部治疗的这种 CD44 靶向治疗策略,针对这种策略,全身化疗几乎无效。