PMID- 26956891 OWN - NLM STAT- MEDLINE DCOM- 20161213 LR - 20181113 IS - 1477-7819 (Electronic) IS - 1477-7819 (Linking) VI - 14 DP - 2016 Mar 8 TI - Downregulation of selenium-binding protein 1 is associated with poor prognosis in lung squamous cell carcinoma. PG - 70 LID - 10.1186/s12957-016-0832-6 [doi] LID - 70 AB - BACKGROUND: We found that selenium-binding protein 1 (SBP1) was progressively decreased in the human bronchial epithelial carcinogenic processes. Knockdown of SBP1 in immortalized human bronchial epithelial cell line 16HBE cells significantly increased the efficiency of B[a]P-induced cell transformation. However, the relationship between SBP1 expression and clinicopathological factors of patients has not been defined completely. The specific role of SBP1 in prognosis of lung squamous cell carcinoma (LSCC) is still unknown. METHODS: Tissue samples from 82 patients treated by pulmonary lobectomy for LSCC were used. Immunohistochemistry and western blotting were used to detect the expressions of SBP1 protein. The relationships between the expression level of SBP1 and the clinicopathological features of patients were analyzed. Cox proportional hazard regression analysis and Kaplan-Meier method were used to perform survival analysis. RESULTS: Expressions of SBP1 proteins were significantly lower in LSCC tissues than that in the corresponding normal bronchial epithelium (NBE) tissues (P = 0.000). In LSCC, The expression levels of SBP1 had not correlated with patients' age, gender, smoking state, primary tumor stages (T), TNM clinical stages, and distant metastasis (M) (P > 0.05). However, downregulation of SBP1 was significantly associated with higher lymph node metastasis and lower overall survival rate (P < 0.05). Cox regression analysis indicated low expressions of SBP1 can be an independent prognostic factor for poor overall survival in LSCC patients (P = 0.002). CONCLUSIONS: Downregulation of SBP1 may play a key role in the tumorigenic process of LSCC. SBP1 may be a novel potential prognostic factor of LSCC. FAU - Tan, Xing AU - Tan X AD - School of Nursing, University of South China, 28# Changsheng Road West, Hengyang, 421001, Hunan, China. 445679540@qq.com. FAU - Liao, Li AU - Liao L AD - School of Nursing, University of South China, 28# Changsheng Road West, Hengyang, 421001, Hunan, China. 254251558@qq.com. FAU - Wan, Yan-Ping AU - Wan YP AD - School of Nursing, University of South China, 28# Changsheng Road West, Hengyang, 421001, Hunan, China. wanyy1991@aliyun.com. FAU - Li, Mei-Xiang AU - Li MX AD - School of Medicine, University of South China, Hengyang, 421001, China. meixiangle@163.com. FAU - Chen, Si-Han AU - Chen SH AD - School of Medicine, University of South China, Hengyang, 421001, China. 172140411@qq.com. FAU - Mo, Wen-Juan AU - Mo WJ AD - School of Nursing, University of South China, 28# Changsheng Road West, Hengyang, 421001, Hunan, China. 764971367@qq.com. FAU - Zhao, Qiong-Lan AU - Zhao QL AD - School of Nursing, University of South China, 28# Changsheng Road West, Hengyang, 421001, Hunan, China. 386212360@qq.com. FAU - Huang, Li-Fang AU - Huang LF AD - School of Nursing, University of South China, 28# Changsheng Road West, Hengyang, 421001, Hunan, China. 450392434@qq.com. FAU - Zeng, Gu-Qing AU - Zeng GQ AD - School of Nursing, University of South China, 28# Changsheng Road West, Hengyang, 421001, Hunan, China. zengguqing0123@163.com. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20160308 PL - England TA - World J Surg Oncol JT - World journal of surgical oncology JID - 101170544 RN - 0 (Biomarkers, Tumor) RN - 0 (Selenium-Binding Proteins) SB - IM MH - Biomarkers, Tumor/*metabolism MH - Blotting, Western MH - Carcinoma, Squamous Cell/metabolism/*secondary MH - Down-Regulation MH - Female MH - Follow-Up Studies MH - Humans MH - Immunoenzyme Techniques MH - Lung Neoplasms/metabolism/*pathology MH - Lymphatic Metastasis MH - Male MH - Middle Aged MH - Neoplasm Staging MH - Prognosis MH - Selenium-Binding Proteins/*metabolism MH - Survival Rate PMC - PMC4782367 EDAT- 2016/03/10 06:00 MHDA- 2016/12/15 06:00 PMCR- 2016/03/08 CRDT- 2016/03/10 06:00 PHST- 2015/07/30 00:00 [received] PHST- 2016/03/01 00:00 [accepted] PHST- 2016/03/10 06:00 [entrez] PHST- 2016/03/10 06:00 [pubmed] PHST- 2016/12/15 06:00 [medline] PHST- 2016/03/08 00:00 [pmc-release] AID - 10.1186/s12957-016-0832-6 [pii] AID - 832 [pii] AID - 10.1186/s12957-016-0832-6 [doi] PST - epublish SO - World J Surg Oncol. 2016 Mar 8;14:70. doi: 10.1186/s12957-016-0832-6.