表型
嗜铬细胞瘤
神经嵴
生物
病态的
癌症
癌症研究
多发性内分泌肿瘤
内分泌系统
受体
胰岛素样生长因子1受体
生长因子
内分泌学
内科学
医学
激素
遗传学
基因
作者
P. Pennisi,María Celia Fernández,Ayelén Martín
出处
期刊:PubMed
日期:2020-08-01
卷期号:17 (4): 331-342
被引量:1
标识
DOI:10.17458/per.vol17.2020.kc.insightspheochromocytomabiology
摘要
Pheochromocytomas/paragangliomas (PCCs/PGLs) are rare neuroendocrine tumors, developed from chromaffin cells derived from the neural crest. From a genetic point of view PCCs/PGLs are divided as sporadic cases, and inherited cases as part of hereditary (familial) syndromes. While the majority is benign, up to 26% of PCCs/PGLs will undergo malignant transformation. Validated prognostic pathological parameters for malignant PCCs/PGLs are still lacking. Signaling that follows the interactions between IGFs and their receptor/s in tumor cells received extensive attention when investigating the role of IGF1R in cancer. Increased IGF1R expression has been shown during progression to metastatic phenotypes and associated with worse prognosis in several types of cancer. In this review we provide evidence supporting a role for the IGFs system on PCC/PGL tumor biology and malignant behavior, endocrine actions to sustain tumor phenotype as well as heterotypic interaction´s regulation by IGF1, encouraging further research for targeted therapeutic options for these tumors.
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