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S100B 蛋白可能参与 NSCLC 的脑转移。

S100B protein as a possible participant in the brain metastasis of NSCLC.

机构信息

Department of Oncology, Tangdu Hospital, Fourth Military Medical University, 1 Xinsi Road, Xi’an 710038, China.

出版信息

Med Oncol. 2012 Dec;29(4):2626-32. doi: 10.1007/s12032-012-0169-0.

DOI:10.1007/s12032-012-0169-0
PMID:22286962
Abstract

Brain metastasis is a frequent occurrence in lung cancer, especially non-small cell lung cancer (NSCLC), the prognosis for NSCLC with brain metastasis is very poor. Our previous study found high S100B expression in the brain-specific metastatic NSCLC line PC14/B, suggested S100B is closely correlated with brain metastasis in NSCLC. However, the details have not yet been revealed. The aim of this study was to investigate the correlation between S100B and brain metastasis in NSCLC and to study the effects of S100B on non-brain metastatic NSCLC line PC14. We investigated serum S100B levels in 30 newly diagnosed NSCLC patients (15 with brain metastasis and 15 without brain metastasis) using enzyme-linked immunosorbent assay. Results showed that serum S100B levels were significant higher in NSCLC patients with brain metastasis compared to those without brain metastasis (P<0.01). We constructed the full-length S100B expression vector and transfected into PC14 cells. MTT and flow cytometric analysis showed that S100B transfection promoted cell proliferation and inhibited cell apoptosis (P<0.05). Transwell migration and invasion assays indicated that S100B transfection promoted cell invasion and cell migration compared to control cells transfected with empty vector alone (P<0.01). These results suggested that S100B could be involved in the development of brain metastasis in NSCLC.

摘要

脑转移是肺癌的常见并发症,尤其是非小细胞肺癌(NSCLC)。脑转移的 NSCLC 患者预后极差。我们之前的研究发现,脑特异性转移性 NSCLC 细胞系 PC14/B 中 S100B 表达较高,提示 S100B 与 NSCLC 的脑转移密切相关。然而,具体细节尚未揭示。本研究旨在探讨 S100B 与 NSCLC 脑转移的相关性,并研究 S100B 对非脑转移性 NSCLC 细胞系 PC14 的影响。我们采用酶联免疫吸附试验检测了 30 例初诊 NSCLC 患者(15 例有脑转移,15 例无脑转移)血清 S100B 水平。结果显示,有脑转移的 NSCLC 患者血清 S100B 水平明显高于无脑转移患者(P<0.01)。我们构建了全长 S100B 表达载体并转染至 PC14 细胞。MTT 和流式细胞术分析表明,S100B 转染促进了细胞增殖,抑制了细胞凋亡(P<0.05)。Transwell 迁移和侵袭实验表明,与单独转染空载体的对照细胞相比,S100B 转染促进了细胞侵袭和迁移(P<0.01)。这些结果表明,S100B 可能参与了 NSCLC 脑转移的发生。

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