ORIGINAL ARTICLE
The prognostic significance of CD63 expressionin patients with non-small cell lung cancer
,
 
,
 
,
 
 
 
 
More details
Hide details
1
Department of Pathology, Gyeongsang National University Changwon Hospital, South Korea
 
2
Department of Thoracic and Cardiovascular Surgery, Gyeongsang National University Changwon Hospital, South Korea
 
3
Gyeongsang National University School of Medicine, South Korea
 
4
Gyeongsang Institute of Health Science, South Korea
 
 
Submission date: 2019-01-10
 
 
Final revision date: 2019-03-11
 
 
Acceptance date: 2019-04-27
 
 
Publication date: 2019-12-08
 
 
Pol J Pathol 2019;70(3):183-188
 
KEYWORDS
TOPICS
ABSTRACT
CD63 has been suggested to participate in tumorigenesis, invasion, and metastasis. In this study, we aimed to investigate the prognostic significance of CD63 expression in non-small cell lung cancer (NSCLC).
CD63 expression was evaluated in 133 cases of NSCLC via immunohistochemical staining using tissue microarray blocks. We assessed the relationship between CD63 expression and clinicopathological characteristics, as well as the prognostic significance of CD63 expression in NSCLC.
CD63 expression was significantly correlated with patient gender (p < 0.001), smoking history (p = 0.020), histologic type (p < 0.001), tumour stage (p = 0.016), lymph node metastasis (p = 0.034), and TNM stage (p = 0.007). A multivariate Cox proportional hazards regression analysis determined low CD63 expression to be an independent factor for unfavourable disease-free survival (DFS) (HR = 2.043, 95% CI: 1.035-4.035, p = 0.040), and Kaplan-Meier analysis indicated that the low CD63 expression group showed significantly lower DFS than the high CD63 expression group of patients with NSCLC (p = 0.019).
Low CD63 expression might be an unfavourable prognostic factor in patients with NSCLC.
REFERENCES (24)
1.
Li L, Sun Y, Feng M, et al. Clinical significance of bloodbased miRNAs as biomarkers of nonsmall cell lung cancer. Oncol Lett 2018; 15: 8915-8925.
 
2.
Ku BM, Heo MH, Kim JH, et al. Molecular screening of small biopsy samples using next-generation sequencing in korean patients with advanced non-small cell lung cancer: Korean lung cancer consortium (KLCC-13-01). J Pathol Transl Med 2018; 52: 148-156.
 
3.
Jo YM, Park TI, Lee HY, et al. Prognostic significance of aquaporin 5 expression in non-small cell lung cancer. J Pathol Transl Med 2016; 50: 122-128.
 
4.
Campa MJ, Wang MZ, Howard B, et al. Protein expression profiling identifies macrophage migration inhibitory factor and cyclophilin a as potential molecular targets in non-small cell lung cancer. Cancer Res 2003; 63: 1652-1656.
 
5.
Yun S, Sun PL, Jin Y, et al. Aquaporin 1 is an independent marker of poor prognosis in lung adenocarcinoma. J Pathol Transl Med 2016; 50: 251-257.
 
6.
Bandres E, Bitarte N, Arias F, et al. microRNA-451 regulates macrophage migration inhibitory factor production and proliferation of gastrointestinal cancer cells. Clin Cancer Res 2009; 15: 2281-2290.
 
7.
Lai X, Gu Q, Zhou X, et al. Decreased expression of CD63 tetraspanin protein predicts elevated malignant potential in human esophageal cancer. Oncol Lett 2017; 13: 4245-4251.
 
8.
Liu W, Li X, Zhu X, et al. CD63 inhibits the cell migration and invasion ability of tongue squamous cell carcinoma. Oncol Lett 2018; 15: 9033-9042.
 
9.
Jang H, Lee H. A decrease in the expression of CD63 tetraspanin protein elevates invasive potential of human melanoma cells. Exp Mol Med 2003; 35: 317-323.
 
10.
Kang M, Ryu J, Lee D, et al. Correlations between transmembrane 4 L6 family member 5 (TM4SF5), CD151, and CD63 in liver fibrotic phenotypes and hepatic migration and invasive capacities. PLoS One 2014; 9: e102817.
 
11.
Sordat I, Decraene C, Silvestre T, et al. Complementary DNA arrays identify CD63 tetraspanin and α3 integrin chain as differentially expressed in low and high metastatic human colon carcinoma cells. Lab Invest 2002; 82: 1715-1724.
 
12.
Sauer G, Kurzeder C, Grundmann R, et al. Expression of tetraspanin adaptor proteins below defined threshold values is associated with in vitro invasiveness of mammary carcinoma cells. Oncol Rep 2003; 10: 405-410.
 
13.
Zhijun X, Shulan Z, Zhuo Z. Expression and significance of the protein and mRNA of metastasis suppressor gene ME491/CD63 and integrin alpha5 in ovarian cancer tissues. Eur J Gynaecol Oncol 2007; 28: 179-183.
 
14.
Song DH, Ko GH, Lee JH, et al. Prognostic role of myoferlin expression in patients with clear cell renal cell carcinoma. Oncotarget 2017; 8: 89033-89039.
 
15.
Kwon MS, Shin S, Yim S, et al. CD63 as a biomarker for predicting the clinical outcomes in adenocarcinoma of lung. Lung Cancer 2007; 57: 46-53.
 
16.
Kondoh M, Ueda M, Ichihashi M, et al. Decreased expression of human melanoma-associated antigen ME491 along the progression of melanoma pre-canceroses to invasive and metastatic melanomas. Melanoma Res 1993; 3: 241-245.
 
17.
Pols MS, Klumperman J. Trafficking and function of the tetraspanin CD63. Exp Cell Res 2009; 315: 1584-1592.
 
18.
Radford KJ, Mallesch J, Mersey P. Suppression of human melanoma cell growth and metastasis by the melanoma-associated antigen CD63 (ME491). Int J Cancer 1995; 62: 631-635.
 
19.
Radford KJ, Thorne RF, Hersey P. CD63 associates with transmembrane 4 superfamily members, CD9 and CD81, and with β1 integrins in human melanoma. Biochem Biophys Res Commun 1996; 222: 13-18.
 
20.
Radford KJ, Thorne RF, Hersey P. Regulation of tumor cell motility and migration by CD63 in a human melanoma cell line. J Immunol 1997; 158: 3353-3358.
 
21.
Seubert B, Cui H, Simonavicius N, et al. Tetraspanin CD 63 acts as a pro-metastatic factor via β-catenin stabilization. Int J Cancer 2015; 136: 2304-2315.
 
22.
Cui H, Seubert B, Stahl E, et al. Tissue inhibitor of metalloproteinases-1 induces a pro-tumourigenic increase of miR-210 in lung adenocarcinoma cells and their exosomes. Oncogene 2015; 34: 3640-3650.
 
23.
Rorive S, Lopez XM, Maris C, et al. TIMP-4 and CD63: New prognostic biomarkers in human astrocytomas. Mod Pathol 2010; 23: 1418-1428.
 
24.
Toricelli M, Melo FH, Hunger A, et al. Timp1 promotes cell survival by activating the PDK1 signaling pathway in melanoma. Cancers 2017; 9: E37.
 
eISSN:2084-9869
ISSN:1233-9687
Journals System - logo
Scroll to top