Suppr超能文献

奥曲肽和胰岛素对结肠癌细胞增殖的影响及其与端粒酶逆转录酶(hTERT)活性的相关性。

Effects of octreotide and insulin on colon cancer cellular proliferation and correlation with hTERT activity.

作者信息

Ayiomamitis Georgios D, Notas George, Zaravinos Apostolos, Drygiannakis Ioannis, Georgiadou Maria, Sfakianaki Ourania, Mastrodimou Niki, Thermos Kyriaki, Kouroumalis Elias

机构信息

Laboratory of Gastroenterology, School of Medicine, University of Crete, Heraklion, Greece ; 2nd Department of Surgery, Tzaneion General Hospital, Piraeus, Greece.

Laboratory of Gastroenterology, School of Medicine, University of Crete, Heraklion, Greece ; Laboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Greece.

出版信息

Oncoscience. 2014 Jun 30;1(6):457-67. doi: 10.18632/oncoscience.58. eCollection 2014.

Abstract

Peptide hormone somatostatin and its receptors have a wide range of physiological functions and play a role in the treatment of numerous human diseases, including colorectal cancer. Octreotide, a synthetic somatostatin-analog peptide, inhibits growth of colonic cancer cells primarily by binding to G-protein coupled receptors and elicits cellular responses through second-messenger systems. Insulin also initiates mitogenic signals in certain cell types. The objective of the present study was to explore the effects of octreotide with or without insulin treatment, on Caco-2 and HT-29 human colon-cancer cell proliferation and to correlate their effects with the activation of telomerase reverse transcriptase (hTERT). The involvement of protein tyrosine phosphatases in the regulation of the anti-proliferative effect of octreotide was also evaluated. Sodium orthovanadate was used to reverse the anti- proliferative effect of octreotide. Telomerase activity was determined for each time point under octreotide and/or insulin treatment. Elevated expression of sst1, sst2 and sst5 was confirmed in both cell lines by RT-PCR. Immunocytochemistry detected sst1, sst2A, sst2B, sst3, sst4 and sst5 protein expression in the membranes of both cell lines. Octreotide inhibited the proliferation of Caco-2 and HT-29 cells in a time and dose-dependent manner. Insulin exerted proliferative effects in Caco-2 cells and octreotide reversed its effect in both cell lines. Sodium orthovanadate suppressed the anti-proliferative effect of octreotide both in Caco-2 and HT-29 cells. Telomerase activity was significantly reduced when Caco-2 cells were exposed to octreotide, under serum-free cultured medium. On the other hand, telomerase attenuation after octreotide treatment could not counteract the actions of insulin on both cells. Our data indicate that the use of octreotide could provide a possible therapeutic approach to the management of certain patients who suffer from colon cancer.

摘要

肽激素生长抑素及其受体具有广泛的生理功能,在包括结直肠癌在内的多种人类疾病的治疗中发挥作用。奥曲肽是一种合成的生长抑素类似肽,主要通过与G蛋白偶联受体结合来抑制结肠癌细胞的生长,并通过第二信使系统引发细胞反应。胰岛素也在某些细胞类型中启动有丝分裂信号。本研究的目的是探讨奥曲肽联合或不联合胰岛素治疗对Caco-2和HT-29人结肠癌细胞增殖的影响,并将其影响与端粒酶逆转录酶(hTERT)的激活相关联。还评估了蛋白酪氨酸磷酸酶在奥曲肽抗增殖作用调节中的参与情况。用原钒酸钠来逆转奥曲肽的抗增殖作用。在奥曲肽和/或胰岛素处理下的每个时间点测定端粒酶活性。通过RT-PCR在两种细胞系中均证实了sst1、sst2和sst5的表达升高。免疫细胞化学检测到两种细胞系膜中sst1、sst2A、sst2B、sst3、sst4和sst5蛋白的表达。奥曲肽以时间和剂量依赖性方式抑制Caco-2和HT-29细胞的增殖。胰岛素对Caco-2细胞具有增殖作用,而奥曲肽在两种细胞系中均逆转了其作用。原钒酸钠在Caco-2和HT-29细胞中均抑制了奥曲肽的抗增殖作用。在无血清培养基中,当Caco-2细胞暴露于奥曲肽时,端粒酶活性显著降低。另一方面,奥曲肽处理后端粒酶活性的减弱并不能抵消胰岛素对两种细胞的作用。我们的数据表明,使用奥曲肽可能为某些结肠癌患者的治疗提供一种可能的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb5/4284627/ad82751966a4/oncoscience-01-0457-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验