肺癌
转移
血小板
微阵列分析技术
基因
下调和上调
微阵列
基因表达
巨核细胞
转录组
癌症研究
选择性拼接
生物
血小板活化
癌症
RNA剪接
信使核糖核酸
医学
免疫学
病理
内科学
核糖核酸
遗传学
干细胞
造血
作者
David C. Calverley,Tzu Phang,Qamrul G. Choudhury,Bifeng Gao,Ana B. Oton,Michael J. Weyant,Mark W. Geraci
标识
DOI:10.1111/j.1752-8062.2010.00226.x
摘要
Abstract Platelets play a major role in the metastatic dissemination of tumor cells in vivo . Recent evidence reveals megakaryocyte‐derived platelet pre‐mRNA is spliced to mRNA and then translated into functional proteins in response to external stimulation. Employing a human lung cancer model, we hypothesized a subset of megakaryocyte/platelet genes exists that are significantly over or underexpressed in metastasis compared with noncancer. Microarray analysis employing platelet mRNA followed by unsupervised hierarchical clustering revealed an expression profile that includes decreased expression of 197 of the 200 platelet genes with the most altered expression ( p < 1.0 × 10 −4 ). Among the 608 splicing events identified between the metastasis and negative control groups, 33 highly variable genes were identified with between 3 and 13 splicing events each. In conclusion, this preliminary study reveals a platelet‐based gene expression signature that differentiates metastatic lung cancer from negative controls on the basis of decreased expression of 197 of the 200 genes with the most altered expression levels. Further study may yield a prognostic tool for future metastasis among subsets of early stage lung cancer patients. Clin Trans Sci 2010; Volume 3: 227–232
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