Oncology Research Centre of Mercogliano, Avellino, Italy.
Curr Genomics. 2010 Nov;11(7):513-8. doi: 10.2174/138920210793175903.
Lung cancer is the leading cause of cancer deaths worldwide among both men and women, with more than 1 million deaths annually. Non-small cell lung cancer (NSCLC) accounts for about 80% of all lung cancers.Although recent advances have been made in diagnosis and treatment strategies, the prognosis of NSCLC patients is poor and it is basically due to a lack of early diagnostic tools.However, in the last years genetic and biochemical studies have provided more information about the protein and gene's mutations involved in lung tumors. Additionally, recent proteomic and microRNA's approaches have been introduced to help biomarker discovery.Here we would like to discuss the most recent discoveries in lung cancer pathways, focusing on the genetic and epigenetic factors that play a crucial role in malignant cell proliferation, and how they could be helpful in diagnosis and targeted therapy.
肺癌是全世界男性和女性癌症死亡的主要原因,每年有超过 100 万人死亡。非小细胞肺癌(NSCLC)约占所有肺癌的 80%。尽管在诊断和治疗策略方面取得了一些进展,但 NSCLC 患者的预后仍然很差,这主要是由于缺乏早期诊断工具。然而,在过去几年中,遗传和生化研究提供了更多关于参与肺癌肿瘤的蛋白质和基因突变的信息。此外,最近还引入了蛋白质组学和 microRNA 方法来帮助发现生物标志物。在这里,我们将讨论肺癌途径的最新发现,重点讨论在恶性细胞增殖中起关键作用的遗传和表观遗传因素,以及它们如何有助于诊断和靶向治疗。