Overexpression of SCC-S2 correlates with lymph node metastasis and poor prognosis in patients with non-small-cell lung cancer

被引:88
作者
Dong, Qian-Ze
Zhao, Yue
Liu, Yang
Wang, Yang
Zhang, Peng-Xin
Jiang, Gui-Yang
Dong, Xin-Jun
Cui, Quan-Ze
Wang, En-Hua [1 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Dept Pathol, Shenyang, Peoples R China
基金
中国国家自然科学基金;
关键词
DEATH EFFECTOR DOMAIN; MATRIX METALLOPROTEINASES; COLORECTAL-CANCER; MMP-9; EXPRESSION; IDENTIFICATION; ANGIOGENESIS; RECEPTORS; APOPTOSIS; BIOLOGY;
D O I
10.1111/j.1349-7006.2010.01557.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The objective of the current study was to investigate the expression pattern and clinicopathological significance of SCC-S2 in patients with non-small-cell lung cancer (NSCLC). The expression profile of SCC-S2 in NSCLC tissues and adjacent noncancerous lung tissues was detected by real-time RT-PCR, western blot analysis, and immunohistochemistry. In 25 lung cancer tissues examined, 18 (72%) of them exhibited stronger levels of SCC-S2 mRNA compared with their corresponding normal tissues. SCC-S2 protein level was up-regulated in cancerous lung tissues compared to adjacent normal tissue. Moreover, the expression level of SCC-S2 in 93 archived NSCLC tissues was measured by immunohistochemical staining. SCC-S2 was found to be overexpressed in 71 of 93 (76.3%) human lung cancer samples and correlated with lymph node metastasis (P = 0.0181), p-TNM stage (P = 0.0042), Ki-67 expression (P = 0.0028), and poor survival (P = 0.012). In addition, depleting SCC-S2 expression by small-interfering RNA inhibited growth and invasion in lung cell lines. These results indicate that SCC-S2 plays an important role in NSCLC and might be a useful therapeutic target of NSCLC. (Cancer Sci 2010).
引用
收藏
页码:1562 / 1569
页数:8
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