Identification of enhancer of zeste homolog 2 expression in peripheral circulating tumor cells in metastatic prostate cancer patients: A preliminary study

被引:8
作者
Cho, Kang Su [1 ]
Oh, Hea Young [1 ,2 ]
Lee, Eun Jin [1 ]
Hong, Sung Joon [1 ]
机构
[1] Yonsei Univ, Coll Med, Dept Urol, Urol Sci Inst,Brain Korea Project Med Sci 21, Seoul 120752, South Korea
[2] Yonsei Univ, Dept Food & Nutr, Seoul 120752, South Korea
关键词
prostate cancer; metastasis; circulating tumor cell; enhancer of zeste homolog 2;
D O I
10.3349/ymj.2007.48.6.1009
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Purpose: Enhancer of zeste homolog 2 (EZH2), a kind of transcriptional repressor, is reportedly over-expressed in metastatic prostate cancer. In this study, we analyzed EZH2 mRNA in circulating tumor cells (CTCs) in peripheral blood as a biomarker in patients with metastatic prostate cancer. Patients and Methods: Ber-EP4 coated immunomagnetic beads were used to harvest CTCs, and mRNA was isolated by oligo-dT conjugated immunomagnetic beads. Reverse transcriptase-polymerase chain reaction for EZH2 mRNA was performed and the expression density was measured. The sensitivity of this test for detection of EZH2 mRNA was determined by serial dilutions of a human prostate cancer cell line. Blood samples were collected from 20 patients each with metastatic or localized prostate cancer and 10 healthy volunteers. Results: Sensitivity experiments showed that the test was highly sensitive as it could detect 10 tumor cells per 5mL. EZH2 mRNA expression was obtained from peripheral blood samples of patients and control subjects. EZH2 mRNA expression density in the metastatic prostate cancer group was significantly higher than in the control (p=0.023) and localized prostate cancer groups (p=0.019). There was no difference between the control and localized prostate cancer groups (p > 0.05). Conclusion: EZH2 mRNA expression in circulating epithelial cells represents a promising marker for detecting early metastasis in prostate cancer. However, more specific and sensitive techniques for detection of CTCs are needed to avoid mononuclear cell contamination.
引用
收藏
页码:1009 / 1014
页数:6
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