Targeted chemotherapy using a cytotoxic somatostatin conjugate to inhibit tumor growth and metastasis in nude mice.

Clinical medicine. Oncology Pub Date : 2008-01-01 Epub Date: 2008-08-19 DOI:10.4137/cmo.s970
Li-Chun Sun, L Vienna Mackey, Jing Luo, Joseph A Fuselier, David H Coy
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引用次数: 29

Abstract

The major problems of traditional chemotherapy are non-selectivity and non-specificity, resulting in severe toxic side effects. Peptides are a new-generation of drug-delivery vector to increase efficacy of this therapy and avoid the resulting damage. The cytotoxic somatostatin (SST) conjugate JF-10-81 was developed by coupling camptothecin (CPT) to the N-terminus of a SST analog (JF-07-69) using an activated carbamate linker. This conjugate selectively targets somatostatin receptor subtype 2 (SSTR2) and also retains high binding affinity and rapid internalization as well as anti-proliferative activity towards various tumor cells. JF-10-81 was tested for its inhibitory activity against the growth of human tumors which included neuroblastoma (IMR32), pancreatic cancer (CFPAC-1), leukemia (MOLT-4), pancreatic carcinoid (BON) and prostate cancer (PC-3). Both SSTR2 mRNAs and proteins were detected in all these tumor cell lines. The conjugate displayed potent in vivo inhibitory activity, although some of the potency measured in in vitro experiments was lost. JF-10-81 was found to significantly inhibit growth of these SSTR-positive tumors, resulting in 87% tumor reduction in neuroblastoma IMR32 and 97% in leukemia MOLT-4 bearing animals, even inducing regression of CFPAC-1 tumors. SSTR-overexpressing BON tumors were unfortunately relatively CPT-insensitive in vitro, however, JF-10-81 again exhibited in vivo potency presumably by specifically increasing CPT concentrations inside the tumor cells so that the inhibition rate for JF-10-81 was 85%. Also, JF-10-81 was used to treat highly invasive PC-3 tumors where s.c. injections inhibited both tumor growth (almost 60% reduction) and tumor metastasis (over 70%). This conjugate demonstrated its broad and excellent anti-tumor activity by targeting SSTR2-specific tumor tissues, supporting that short peptides and their analogs may be applied as ideal drug-delivery carriers to improve the traditional chemotherapy.

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使用细胞毒性生长抑素偶联物的靶向化疗抑制裸鼠肿瘤生长和转移。
传统化疗存在的主要问题是非选择性和特异性,毒副作用严重。多肽是一种新一代的药物传递载体,可以提高这种治疗的疗效,避免由此产生的损害。通过活化氨基甲酸酯连接物将喜树碱(CPT)偶联到SST类似物(JF-07-69)的n端,开发了细胞毒性生长抑素(SST)偶联物JF-10-81。该偶联物选择性靶向生长抑素受体亚型2 (SSTR2),并对多种肿瘤细胞保持高结合亲和力和快速内化以及抗增殖活性。JF-10-81对神经母细胞瘤(IMR32)、胰腺癌(CFPAC-1)、白血病(MOLT-4)、类胰腺癌(BON)、前列腺癌(PC-3)等肿瘤的生长有抑制作用。在所有肿瘤细胞系中均检测到SSTR2 mrna和蛋白。该偶联物在体内表现出有效的抑制活性,尽管在体外实验中测量的一些效力丢失了。研究发现JF-10-81显著抑制这些sstr阳性肿瘤的生长,使神经母细胞瘤IMR32的肿瘤减少87%,白血病MOLT-4的肿瘤减少97%,甚至诱导CFPAC-1肿瘤的消退。不幸的是,sstr过表达的BON肿瘤在体外对CPT相对不敏感,然而,JF-10-81再次表现出体内效力,可能是通过特异性增加肿瘤细胞内CPT浓度,因此JF-10-81的抑制率为85%。此外,JF-10-81用于治疗高度侵袭性PC-3肿瘤,其中sc注射抑制肿瘤生长(几乎减少60%)和肿瘤转移(超过70%)。该偶联物可靶向sstr2特异性肿瘤组织,具有广泛而优异的抗肿瘤活性,支持短肽及其类似物可作为理想的药物递送载体,改善传统化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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