期刊
CLINICAL & EXPERIMENTAL METASTASIS
卷 31, 期 7, 页码 841-851出版社
SPRINGER
DOI: 10.1007/s10585-014-9675-0
关键词
Brain metastases; Non-small cell lung cancer; Integrins; Survival
类别
资金
- Medical University of Vienna
Integrins are transmembranous adhesion molecules postulated to be involved in the brain metastatic cascade. We investigated the correlation of alpha v beta 3 (alpha v beta 3), alpha v beta 5 (alpha v beta 5) and alpha v beta 6 (alpha v beta 6) integrin isoform expression with clinical characteristics including survival times in lung cancer patients with brain metastases (BM). All BM from lung cancer operated at our institution between 1990 and 2011, were identified; where available, primary tumors were retrieved as well. Immunohistochemical analysis for alpha v beta 3, alpha v beta 5 and alpha v beta 6 integrin subunits was performed and correlated with Ki67 and hypoxia-inducible factor (HIF)-1 alpha indexes. Clinical data including survival data were obtained by chart review. 191 BM specimens of 191 patients with histologically confirmed lung cancer (172 non-small cell lung cancer and 19 small cell lung cancer) were included. In 18 patients matched primary tumor samples were available. alpha v beta 6 expression was commonly found on BM tumor cells (103/191; 53.9 %) and showed a significant association with low Ki67 proliferation indices (46 vs. 36 %, p = 0.001, Mann-Whitney U test) and favorable survival times (p = 0.020; log rank test) in patients with non-squamous NSCLC BM. alpha v beta 5 expression was highly expressed on vascular structures (167/191; 87.4 %) and tumor stroma in BM (151/191; 79.1 %) and associated with high HIF-1 alpha indices (60 vs. 90, p = 0.007, Mann-Whitney U test). alpha v beta 3 expression was more frequently found on vascular structures in BM than in primary tumors (68.1 vs. 5.6 %; p = 0.645; Chi square test) and its expression in BM tumor cells correlated with low Ki67 indices (41 vs. 28 %; p = 0.046, Mann-Whitney U test). Expression of alpha v integrin subunits seem to be of pathobiological and clinical relevance in patients with NSCLC BM. Further investigations of their involvement in the brain metastatic cascade and their role as biomarkers are warranted.
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