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SOM230 combined with celecoxib prolongs the survival in nude mice with HepG-2 xenografts

机译:SOM230与塞来昔布联合可延长HepG-2异种移植裸鼠的生存期

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摘要

A new non-cytotoxic therapy that SOM230 (pasireotide), a somatostatin analogue (SSTA) combined with celecoxib, a selective cyclooxygenase-2 (COX-2) inhibitor was tested in nude mice bearing HepG2 xenografts. Two agents did not markedly arrest the growth of HepG2 cells but greatly downregulated vascular endothelial growth factor expression. An imbalance between the vigorous demand and insufficient supply of nutrients and oxygen for tumor growth resulted in the massive necrosis of xenografts. The combination synergistically induced the early apoptosis of HepG2 cells and achieved longest survival without adverse reaction. This impressive strategy appears promising as a systemic therapy for patients with hepatocellular carcinoma (HCC).
机译:在带有HepG2异种移植物的裸鼠中测试了一种新的非细胞毒性疗法,该疗法将生长抑素类似物(SSTA)SOM230(帕雷西肽)与选择性环氧化酶2(COX-2)抑制剂塞来昔布联合使用。两种药物没有明显阻止HepG2细胞的生长,但大大下调了血管内皮生长因子的表达。肿瘤生长的旺盛需求与营养和氧气供应不足之间的不平衡导致异种移植物大量坏死。该组合物协同诱导了HepG2细胞的早期凋亡,并获得了最长的生存期而没有不良反应。这种令人印象深刻的策略作为肝癌(HCC)患者的全身疗法似乎很有希望。

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