Hiroshima Cancer Seminar Foundation, Hiroshima, Japan.
Jpn J Clin Oncol. 2010 Jul;40(7):702-8. doi: 10.1093/jjco/hyq031. Epub 2010 Mar 25.
This symposium presented recent progress of the pathogenesis and treatment of lung cancer. Aberrantly increased expression of miR-21 plays a significant role in lung carcinogenesis and is a potential therapeutic target in both epidermal growth factor receptor-mutant and wild-type cases. miR-34 may be necessary for the radiation-induced DNA damage response. Detailed expression profiling analyses of transcriptome have potential to provide increased understanding of the molecular biology of lung cancer. An embryonic signature is present in lung adenocarcinoma only, associated with a worse clinical outcome. Cytoplasmic expression of caveolin and membranous expression of CD26 are specific to mesothelioma. Nectin-4 is a new candidate for serum and tissue biomarker as well as a therapeutic target for lung cancer. Clinical presentations have provided us a great deal information on epidermal growth factor receptor mutations for personalized therapy, combination therapy with inhibitors of the tyrosine kinase activity of epidermal growth factor receptor and cytotoxic agents, antibody-dependent cellular cytotoxicity activity, and current management of lung cancer depending on both the extent of the disease and the treatment approach.
本次研讨会介绍了肺癌发病机制和治疗的最新进展。miR-21 的异常高表达在肺癌发生中起重要作用,是表皮生长因子受体突变型和野生型病例的潜在治疗靶点。miR-34 可能是辐射诱导的 DNA 损伤反应所必需的。对转录组的详细表达谱分析有潜力提供对肺癌分子生物学的更深入理解。胚胎特征仅存在于肺腺癌中,与更差的临床结局相关。细胞质中波形蛋白的表达和膜上 CD26 的表达是间皮瘤的特异性标志物。黏着蛋白-4 是血清和组织生物标志物以及肺癌治疗靶点的新候选物。临床表现为我们提供了大量有关表皮生长因子受体突变的信息,以进行个体化治疗、表皮生长因子受体酪氨酸激酶活性抑制剂与细胞毒性药物的联合治疗、抗体依赖的细胞毒性活性,以及根据疾病程度和治疗方法进行的当前肺癌管理。