|Title:||Human kallikrein 8 protease confers a favorable clinical outcome in non-small cell lung cancer by suppressing tumor cell invasiveness||Authors:||Sher Y.-P.
|Issue Date:||2006||Journal Volume:||66||Journal Issue:||24||Start page/Pages:||11763-11770||Source:||Cancer Research||Abstract:||
The human kallikrein 8 (KLK8) gene, a member of the human tissue kallikrein gene family, encodes a serine protease. The KLK8 protein (hK8) is known to be a favorable prognostic marker in ovarian cancer, but the biological basis of this is not understood. We found that overexpressing the KLK8 gene in highly invasive lung cancer cell lines suppresses their invasiveness. This role in invasiveness was further confirmed by the fact that inhibition of endogenous KLK8 expression with a specific short hairpin RNA reduced cancer cell invasiveness. In situ degradation and cell adhesion assays showed that proteins produced from KLK8 splice variants modify the extracellular microenvironment by cleaving fibronectin. DNA microarray experiments and staining of cells for actin filaments revealed that the degradation of fibronectin by hK8 suppresses integrin signaling and retards cancer cell motility by inhibiting actin polymerization. In addition, studies in a mouse model coupled with the detection of circulating tumor cells by quantitative PCR for the human Alu sequence showed that KLKS suppresses tumor growth and invasion in vivo. Finally, studies of clinical specimens from patients with non-small cell lung cancer showed that the time to postoperative recurrence was longer for early-stage patients (stages I and II) with high KLK8 expression (mean, 49.9 months) than for patients with low KLK8 expression (mean, 22.9 months). Collectively, these findings show that KLK8 expression confers a favorable clinical outcome in non-small cell lung cancer by suppressing tumor cell invasiveness. ?2006 American Association for Cancer Research.
|ISSN:||0008-5472||DOI:||10.1158/0008-5472.CAN-06-3165||SDG/Keyword:||actin; fibronectin; integrin; neuropsin; short hairpin RNA; actin filament; Alu sequence; article; cancer invasion; cancer recurrence; cancer staging; cell adhesion; cell motility; controlled study; DNA microarray; gene expression; genetic transfection; human; human cell; in vivo study; lung non small cell cancer; microenvironment; polymerase chain reaction; postoperative period; priority journal; protein degradation; protein expression; protein polymerization; signal transduction; staining; tumor cell; tumor growth; Base Sequence; Carcinoma, Non-Small-Cell Lung; Cell Adhesion; DNA Primers; Fibronectins; Humans; Kallikreins; Lung Neoplasms; Molecular Sequence Data; Neoplasm Invasiveness; Reverse Transcriptase Polymerase Chain Reaction; Treatment Outcome
|Appears in Collections:||醫學系|
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