Distinct Expression of Surface and Genetic Biomarkers in Prostate Cancer Cell Lines

被引:0
作者
Su, Chen-Ying [1 ]
Huang, Gwo-Che [2 ]
Chen, I-Cheng [3 ]
Chen, Pei-Yu [1 ]
Chen, Yu-Jen [2 ]
Fang, Hsu-Wei [1 ,4 ,5 ]
机构
[1] Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei, Taiwan
[2] MacKay Mem Hosp, Dept Radiat Oncol, Taipei, Taiwan
[3] Natl Taipei Univ Technol, Accelerator Happiness & Hlth Ind, Taipei, Taiwan
[4] Natl Hlth Res Inst, Inst Biomed Engn & Nanomed, Zhunan, Taiwan
[5] Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, 1,Sec 3,Zhongxiao E Rd, Taipei 10608, Taiwan
来源
IN VIVO | 2023年 / 37卷 / 01期
关键词
Surface biomarker; genetic biomarker; prostate cancer; CD44; CD133; PCA3; KLK4; KLK9;
D O I
10.21873/invivo.13073
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: Surface biomarkers, such as CD44 and CD133, have been demonstrated to be expressed in prostate cancer cells, and our previous study has shown that prostate cancer cell lines could be divided into three groups according to the single and combined expression pattern of CD44 and 133. In order to refine prognostication in prostate cancer cells, we further investigated genetic biomarkers, prostate cancer antigen 3 (PCA3), kallikrein 4 (KLK4), and KLK9 in different prostate cancer cell lines. Materials and Methods: CWR22Rv1, PC3, and DU145 cell lines were cultured until 95% confluence. The single expression of CD44 or CD133 and their combined expression were analyzed by flow cytometry, and gene expression of b-actin, PCA3, KLK4, and KLK9 was analyzed by real-time polymerase chain reaction. Results: The single expression of CD133 was less than 4% in all cell lines examined. PC3 and DU145 cells displayed a high expression of CD44 (>91%), whereas CWR22Rv1 was the only cell line that demonstrated a high co-expression of both CD44 and CD133 (>91%). In addition, PC3 and DU145 displayed low expression of PCA3, KLK4, and KLK9 when compared with their own b-actin expression. In contrast, CWR22Rva showed high expression of PCA3 and KLK4 although KLK9 expression was also low. Conclusion: Both surface and genetic biomarkers should be validated for a more accurate prognosis in prostate cancer.
引用
收藏
页码:242 / 246
页数:5
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