Somnay Yash R, Kunnimalaiyaan Muthusamy
Endocrine Surgery Research Laboratories, Department of Surgery, University of Wisconsin School of Medicine and Public Health, and the UW Carbone Cancer Center, Madison 53705, USA.
Glob J Biochem. 2012;3. Epub 2011 Mar 8.
The phosphatidylinositol 3-kinase (PI3K)-Akt pathway is often aberrantly activated in neuroendocrine-derived cancers. Therefore, selectively targeting this pathway using small-molecule inhibitors may reduce neuroendocrine tumor burden, potentiate adjunct therapies, and achieve symptomatic control for patients with hormonally active and inoperable disease. Here, we discuss the role of the PI3K-Akt pathway in the malignant transformation of neuroendocrine tumors, specifically carcinoids and small cell lung cancers. The collective findings presented in this review propose that selective targeting of the PI3K-Akt pathway may mitigate neuroendocrine tumor progression, thus offering a viable therapeutic approach for managing systemic disease.
磷脂酰肌醇3-激酶(PI3K)-Akt信号通路在神经内分泌源性癌症中常被异常激活。因此,使用小分子抑制剂选择性地靶向该信号通路可能会减轻神经内分泌肿瘤负担,增强辅助治疗效果,并为激素活性高且无法手术的患者实现症状控制。在此,我们讨论PI3K-Akt信号通路在神经内分泌肿瘤(特别是类癌和小细胞肺癌)恶性转化中的作用。本综述中呈现的总体研究结果表明,选择性靶向PI3K-Akt信号通路可能会减轻神经内分泌肿瘤的进展,从而为全身性疾病的治疗提供一种可行的治疗方法。