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叶酸靶向长春花生物碱偶联物EC140和EC145的临床前比较活性

Comparative preclinical activity of the folate-targeted Vinca alkaloid conjugates EC140 and EC145.

作者信息

Leamon Christopher P, Reddy Joseph A, Vlahov Iontcho R, Westrick Elaine, Parker Nikki, Nicoson Jeffrey S, Vetzel Marilynn

机构信息

Endocyte, Inc., 3000 Kent Ave., West Lafayette, IN 47906, USA.

出版信息

Int J Cancer. 2007 Oct 1;121(7):1585-92. doi: 10.1002/ijc.22853.

Abstract

EC140 is a water soluble folate conjugate of desacetylvinblastine monohydrazide (DAVLBH), which is constructed with an endosome-cleavable acyl hydrazone bond. This agent has proven to be active and specific against well established, subcutaneous folate receptor (FR)-positive tumors in multiple animal models. Recent structure-activity and optimization studies have yielded a disulfide bond-containing counterpart to EC140, herein referred to as EC145. This new conjugate was found to retain high affinity for FR-positive cells, and it produced specific, dose-responsive activity in vitro. Comparative in vivo efficacy tests confirmed that, like EC140, EC145 displays activity against both syngeneic and xenograft tumor models. However, EC145 was found to be more active and better tolerated than EC140; hence, more durable complete responses were consistently observed in EC145-treated tumor-bearing animals. Furthermore, EC145 was not found to be active against a FR-negative tumor model. Additional preclinical studies are therefore warranted to better understand EC145's breadth of activity against FR-positive tumors.

摘要

EC140是去乙酰长春碱单酰肼(DAVLBH)的水溶性叶酸偶联物,它通过一种可在内体裂解的酰腙键构建而成。该药物已被证明对多种动物模型中已确立的皮下叶酸受体(FR)阳性肿瘤具有活性且具有特异性。最近的构效关系和优化研究产生了一种含二硫键的EC140类似物,在此称为EC145。发现这种新的偶联物对FR阳性细胞保持高亲和力,并且在体外产生特异性的剂量反应活性。体内疗效比较试验证实,与EC140一样,EC145对同基因和异种移植肿瘤模型均有活性。然而,发现EC145比EC140更具活性且耐受性更好;因此,在接受EC145治疗的荷瘤动物中始终观察到更持久的完全缓解。此外,未发现EC145对FR阴性肿瘤模型有活性。因此,需要进行更多的临床前研究,以更好地了解EC145对FR阳性肿瘤的活性广度。

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