Liwen Chen1, Guangbo Zhang2, Shouqin Sheng3, Qiang Zhou1, Ying Pan1, Shihe Guan4. 1. Department of Laboratory Medicine, The Second Hospital of Anhui Medical University, Hefei, China. 2. Clinical Immunology Laboratory and Institute of Medical Biotechnology, Soochow University, Suzhou, China. 3. Medical Research Center, The Second Hospital of Anhui Medical University, Hefei, China. 4. Department of Laboratory Medicine, The Second Hospital of Anhui Medical University, Hefei, China. Electronic address: shiheguan@126.com.
Abstract
BACKGROUND: The B7 family member B7-H3 (CD276) is involved in tumor immunity including Non-small-cell lung cancer (NSCLC). We have previously demonstrated an elevated circulating level of the soluble form of B7-H3 (sB7-H3) in NSCLC patients. However, the expression of sB7-H3 in NSCLC-derived malignant pleural effusions (MPEs) and its clinical significance remain elusive. METHODS: We measured and compared sB7-H3 levels in NSCLC-derived MPEs (n=52) and nonneoplastic pleural effusions (NPEs) (n=47), and then evaluated the diagnostic performance for sB7-H3 in NSCLC-derived MPEs. The correlation between MPE-derived sB7-H3 and clinical characteristics including TNM staging system was also analyzed. RESULTS: The median value of sB7-H3 in 52 MPEs and 47 NPEs were 41.60ng/ml (interquartile range: 36.76-51.30ng/ml) and 31.55ng/ml (interquartile range: 26.97-36.63ng/ml) (P<0.0001), respectively. At the proposed cut-off value at 38.41ng/ml, sB7-H3 was capable of discriminating NSCLC-derived MPEs from NPEs with a sensitivity of 67.3% and a specificity of 91.5% respectively. Furthermore, MPEs-derived sB7-H3 was correlated with smoking status (P=0.005), primary tumor size (T factor, P=0.03), regional lymph node dissemination (N factor, P=0.019) and distant metastasis (M factor, P=0.009) of NSCLC patients. CONCLUSIONS: Upregulated sB7-H3 expression in MPEs is correlated with TNM stage of NSCLC and may serve as a potential biomarker for NSCLC-derived MPEs.
BACKGROUND: The B7 family member B7-H3 (CD276) is involved in tumor immunity including Non-small-cell lung cancer (NSCLC). We have previously demonstrated an elevated circulating level of the soluble form of B7-H3 (sB7-H3) in NSCLCpatients. However, the expression of sB7-H3 in NSCLC-derived malignant pleural effusions (MPEs) and its clinical significance remain elusive. METHODS: We measured and compared sB7-H3 levels in NSCLC-derived MPEs (n=52) and nonneoplastic pleural effusions (NPEs) (n=47), and then evaluated the diagnostic performance for sB7-H3 in NSCLC-derived MPEs. The correlation between MPE-derived sB7-H3 and clinical characteristics including TNM staging system was also analyzed. RESULTS: The median value of sB7-H3 in 52 MPEs and 47 NPEs were 41.60ng/ml (interquartile range: 36.76-51.30ng/ml) and 31.55ng/ml (interquartile range: 26.97-36.63ng/ml) (P<0.0001), respectively. At the proposed cut-off value at 38.41ng/ml, sB7-H3 was capable of discriminating NSCLC-derived MPEs from NPEs with a sensitivity of 67.3% and a specificity of 91.5% respectively. Furthermore, MPEs-derived sB7-H3 was correlated with smoking status (P=0.005), primary tumor size (T factor, P=0.03), regional lymph node dissemination (N factor, P=0.019) and distant metastasis (M factor, P=0.009) of NSCLCpatients. CONCLUSIONS: Upregulated sB7-H3 expression in MPEs is correlated with TNM stage of NSCLC and may serve as a potential biomarker for NSCLC-derived MPEs.
Authors: Pranav Murthy; Chigozirim N Ekeke; Kira L Russell; Samuel C Butler; Yue Wang; James D Luketich; Adam C Soloff; Rajeev Dhupar; Michael T Lotze Journal: Oncoimmunology Date: 2019-01-22 Impact factor: 8.110