Endocrinology and Nutrition Service, University Hospital of Bellvitge, L´Hospitalet of Llobregat, Spanish Biomedical Research Centre in Diabetes and Associated Metabolic Disorders (CIBERDEM), Barcelona, Spain.
Curr Genomics. 2011 Dec;12(8):597-608. doi: 10.2174/138920211798120826.
The MAPK/ERK (mitogen-activated protein kinase/extracellular signal- regulated kinase signaling pathway) and PI3K/Akt (lipid kinase phoshoinositide-3-kinase signaling pathway) play an important role in transmission of cell signals through transduction systems as ligands, transmembrane receptors and cytoplasmic secondary messengers to cell nucleus, where they influence the expression of genes that regulate important cellular processes: cell growth, proliferation and apoptosis. The genes, coding the signaling cascade proteins (RET, RAS, BRAF, PI3K, PTEN, AKT), are mutated or aberrantly expressed in thyroid cancer derived from follicular thyroid cell. Genetic and epigenetic alternations, concerning MAPK/ERK and PI3K/Akt signaling pathways, contribute to their activation and interaction in consequence of malignant follicular cell transformation. Moreover, it is additionally pointed out that genetic, as well as epigenetic DNA changing via aberrant methylation of several tumor suppressor and thyroid-specific genes is associated with tumor aggressiveness, being a jointly responsible mechanism for thyroid tumorigenesis. In the present manuscript the currently developed diagnostic and prognostic genetic/epigenetic markers are presented; the understanding of this molecular mechanism provides access to novel molecular therapeutic strategies.
丝裂原活化蛋白激酶/细胞外信号调节激酶(MAPK/ERK)和磷脂酰肌醇 3-激酶/蛋白激酶 B(PI3K/Akt)信号通路在细胞信号转导系统中作为配体、跨膜受体和细胞内第二信使发挥重要作用,将信号传递到细胞核,影响调节重要细胞过程的基因表达:细胞生长、增殖和凋亡。来源于滤泡甲状腺细胞的甲状腺癌中,编码信号转导级联蛋白(RET、RAS、BRAF、PI3K、PTEN、AKT)的基因发生突变或异常表达。MAPK/ERK 和 PI3K/Akt 信号通路的遗传和表观遗传改变导致其激活和相互作用,进而导致恶性滤泡细胞转化。此外,还指出遗传和表观遗传 DNA 的改变,通过几个肿瘤抑制基因和甲状腺特异性基因的异常甲基化,与肿瘤侵袭性相关,是甲状腺肿瘤发生的共同负责机制。本文介绍了目前开发的诊断和预后遗传/表观遗传标志物;对该分子机制的理解为新的分子治疗策略提供了途径。