Redding T W, Schally A V
Proc Natl Acad Sci U S A. 1984 Jan;81(1):248-52. doi: 10.1073/pnas.81.1.248.
Using animal models of acinar and ductal pancreatic cancer, we investigated the effect of analogs of hypothalamic hormones on tumor growth. In Wistar/Lewis rats bearing the acinar pancreatic tumor DNCP-322, chronic administration of [L-5-Br-Trp8]somatostatin-14 significantly decreased tumor weights and volume. Somatostatin-28 and the cyclic hexapeptide analog of somatostatin cyclo(Pro-Phe-D-Trp-Lys-Thr-Phe) failed to influence the growth of this tumor. The agonistic analog of luteinizing hormone-releasing hormone [D-Trp6]LH-RH also significantly decreased tumor weight and volume in this model and reduced testosterone levels and the weights of the ventral prostate and tests. In Syrian hamsters bearing ductal type of pancreatic carcinoma, chronic administration of [L-5-Br-Trp8]somatostatin diminished tumor weights and volume. The percentage change in tumor volume was significantly decreased when compared to control animals. In one experiment, cyclic hexapeptide of somatostatin also inhibited growth of this tumor. [D-Trp6]LH-RH, given twice daily or injected in the form of microcapsules for constant controlled release, significantly decreased tumor weight and volume and suppressed serum testosterone levels. Hamsters castrated 4 days after transplantation of the pancreatic tumors showed a significant decrease in weight and volume of these tumors. This suggests that pancreatic cancers may, at least in part, be sex hormone sensitive. [D-Trp6]LH-RH may decrease the growth of pancreatic carcinomas by suppressing androgens. Somatostatin analogs reduce the growth of pancreatic ductal and acinar cancers, probably by inhibiting the release or stimulatory action of gastrointestinal hormones on tumor cells (or both). Inhibition of animal models of pancreatic tumors by chronic administration of somatostatin analogs and [D-Trp6]LH-RH suggests that these compounds should be considered for the development of a new hormonal therapy for cancer of the pancreas.
利用胰腺腺泡癌和导管癌动物模型,我们研究了下丘脑激素类似物对肿瘤生长的影响。在携带胰腺腺泡肿瘤DNCP - 322的Wistar/Lewis大鼠中,长期给予[L - 5 - Br - Trp8]生长抑素-14可显著降低肿瘤重量和体积。生长抑素-28以及生长抑素的环六肽类似物环(Pro - Phe - D - Trp - Lys - Thr - Phe)对该肿瘤的生长没有影响。促黄体生成素释放激素的激动剂类似物[D - Trp6]LH - RH在该模型中也显著降低了肿瘤重量和体积,并降低了睾酮水平以及腹侧前列腺和睾丸的重量。在患有导管型胰腺癌的叙利亚仓鼠中,长期给予[L - 5 - Br - Trp8]生长抑素可减轻肿瘤重量和体积。与对照动物相比,肿瘤体积的百分比变化显著降低。在一项实验中,生长抑素的环六肽也抑制了该肿瘤的生长。每日两次给予或微胶囊注射以持续控释形式给予的[D - Trp6]LH - RH显著降低了肿瘤重量和体积,并抑制了血清睾酮水平。胰腺肿瘤移植后4天去势的仓鼠,其肿瘤重量和体积显著降低。这表明胰腺癌可能至少部分对性激素敏感。[D - Trp6]LH - RH可能通过抑制雄激素来降低胰腺癌的生长。生长抑素类似物可能通过抑制胃肠激素对肿瘤细胞的释放或刺激作用(或两者兼有)来降低胰腺导管癌和腺泡癌的生长。长期给予生长抑素类似物和[D - Trp6]LH - RH对胰腺肿瘤动物模型的抑制作用表明,这些化合物应被考虑用于开发针对胰腺癌的新型激素疗法。