Pharmaco-Chemistry Department, University of Bari, Bari, Italy.
J Drug Target. 2012 Jan;20(1):1-22. doi: 10.3109/1061186X.2011.611518. Epub 2011 Sep 26.
Ligand targeted therapy (LTT) is a powerful pharmaceutical strategy to achieve selective drug delivery to pathological cells, for both therapeutic and diagnostic purposes, with the advantage of limited side effects and toxicity. This active drug targeting approach is based on the discovery that there are receptors overexpressed on pathological cells, compared to their expression in normal tissues.
The purpose of this article is to review recently published data on LTT with applications, both in the field of cancer therapy and other diseases. Moreover, data on LTT exploiting receptors overexpressed at cytoplasmatic level are also reviewed.
Data were deduced from Medline (PubMed) and SciFinder and their selections were made with preference to papers where the most relevant receptors were involved.
Several groups have reported improved delivery of targeted nanocarriers, as compared to nontargeted ones, to pathological cells. LTT offers several advantages, but there are also limitations in the development of this strategy. Moreover, LTT have shown encouraging results in in vitro and in animal models in vivo; hence their clinical potential awaits investigation.
Recent studies highlight that the ligand density plays an important role in targeting efficacy. Furthermore, LTT applications in diseases different from cancer and those exploiting receptors overexpressed at cytoplasmatic level are growing.
配体靶向治疗(LTT)是一种将药物靶向递送至病理细胞的有力制药策略,具有治疗和诊断的双重作用,同时具有副作用和毒性有限的优点。这种主动药物靶向方法基于这样的发现,即在病理细胞上表达的受体比在正常组织中表达的受体更多。
本文的目的是综述最近发表的关于配体靶向治疗的应用数据,包括癌症治疗和其他疾病领域的应用。此外,还综述了利用细胞质水平过表达的受体进行配体靶向治疗的数据。
数据来自 Medline(PubMed)和 SciFinder,并优先选择涉及最相关受体的论文进行选择。
一些研究小组报告称,与非靶向纳米载体相比,靶向纳米载体能够更有效地递送至病理细胞。配体靶向治疗具有多种优势,但在该策略的开发中也存在局限性。此外,配体靶向治疗在体外和体内动物模型中显示出令人鼓舞的结果,因此其临床潜力有待进一步研究。
最近的研究强调了配体密度在靶向效果中的重要作用。此外,配体靶向治疗在癌症以外的疾病中的应用以及利用细胞质水平过表达的受体的应用正在不断增加。