Gene Expression Core--Human Molecular Genetics Laboratory, Institute of Genetics and Biophysics, CNR Naples Italy.
Curr Cancer Drug Targets. 2010 Feb;10(1):19-26. doi: 10.2174/156800910790980232.
Malignant mesothelioma (MM) is a rare, highly aggressive tumor that arises from the surface serosal cells (pleural, peritoneal and pericardial cavities). Epidemiological and clinical data show that there is an association between asbestos exposure and MM development, even if the exact mechanism whereby asbestos induces MM is unknown. The continuing identification and elucidation of the molecular defects involved in mesothelioma pathogenesis and progression should lead to better disease control and greater therapeutic options in the near future. Goal of this article is to summarize the most recent advances in molecular pathogenesis of mesothelioma with particular emphasis on genes that could be considered as biomarkers or therapeutic targets and discuss possible clinical implications of these findings.
恶性间皮瘤(MM)是一种罕见的、侵袭性很强的肿瘤,起源于表面浆膜细胞(胸膜、腹膜和心包腔)。流行病学和临床数据表明,石棉暴露与 MM 的发生之间存在关联,尽管石棉诱导 MM 的确切机制尚不清楚。不断发现和阐明间皮瘤发病机制和进展中涉及的分子缺陷,应能在不久的将来更好地控制疾病和提供更多的治疗选择。本文的目的是总结间皮瘤分子发病机制的最新进展,特别强调可作为生物标志物或治疗靶点的基因,并讨论这些发现的可能临床意义。