Identification of candidate nasopharyngeal carcinoma serum biomarkers by cancer cell secretome and tissue transcriptome analysis: Potential usage of cystatin A for predicting nodal stage and poor prognosis

被引:41
作者
Chang, Kai-Ping [2 ,3 ]
Wu, Chih-Ching [3 ]
Chen, Hua-Chien [3 ]
Chen, Shu-Jen [3 ]
Peng, Pei-Hua [1 ]
Tsang, Ngan-Ming [4 ]
Lee, Li-Yu [5 ]
Liu, Shiau-Chin [2 ]
Liang, Ying [3 ]
Lee, Yun-Shien [6 ]
Hao, Sheng-Po [2 ]
Chang, Yu-Sun [1 ,3 ]
Yu, Jau-Song [1 ,3 ]
机构
[1] Chang Gung Univ, Grad Inst Biomed Sci, Tao Yuan, Taiwan
[2] Chang Gung Mem Hosp, Dept Otolaryngol Head & Neck Surg, Tao Yuan, Taiwan
[3] Chang Gung Univ, Mol Med Res Ctr, Tao Yuan, Taiwan
[4] Chang Gung Mem Hosp, Dept Radiat Oncol, Tao Yuan, Taiwan
[5] Chang Gung Mem Hosp, Dept Pathol, Tao Yuan, Taiwan
[6] Chang Gung Mem Hosp, Genom Med Res Core Lab, Tao Yuan, Taiwan
关键词
Biomarker; Biomedicine; Cystatin A; Nasopharyngeal carcinoma; Secretome; Transcriptome; MANGANESE SUPEROXIDE-DISMUTASE; EPSTEIN-BARR-VIRUS; MATRIX-METALLOPROTEINASE EXPRESSION; LASER CAPTURE MICRODISSECTION; MEMBRANE PROTEIN-1 GENE; CATHEPSIN-B; COLORECTAL-CARCINOMA; PROTEOMIC ANALYSIS; STEFIN-A; IMMUNOHISTOCHEMICAL EXPRESSION;
D O I
10.1002/pmic.200900620
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nasopharyngeal carcinoma (NPC) is usually diagnosed at advanced clinical stages, resulting in poor outcomes. To discover serum biomarkers for improved NPC diagnosis and/or management, we simultaneously analyzed the NPC cell secretome and tissue transcriptome to identify candidate genes/proteins that are highly upregulated in NPC tissues and also secreted/released from NPC cells. Among the 30 candidates identified, 11 proteins were chosen for further validation using the serum samples from NPC patients and healthy controls, including cystatin A, cathepsin B, manganese superoxide dismutase and matrix metalloproteinase 2. The results showed that serum levels of all the four proteins were indeed higher in NPC patients versus healthy controls and that the use of a three-marker panel (cystatin A, manganese superoxide dismutase and matrix metalloproteinase 2) can contribute to a better NPC detection than each marker alone. In addition, a higher pretreated serum level of cystatin A was found to be associated with a higher nodal stage and poorer prognosis of NPC patients and cystatin A could modulate the migration and invasion of NPC cells in vitro. Altogether, our results indicate that analysis of both the cancer cell secretome and tissue transcriptome is a feasible strategy for efficient identification of novel NPC serum marker panel.
引用
收藏
页码:2644 / 2660
页数:17
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