广东医学
廣東醫學
엄동의학
GUNAGDONG MEDICAL JOURNAL
2015年
2期
208-211
,共4页
冉永刚%游颜杰%黄继红%李文梅%苑艺%李海军%赵新雷
冉永剛%遊顏傑%黃繼紅%李文梅%苑藝%李海軍%趙新雷
염영강%유안걸%황계홍%리문매%원예%리해군%조신뢰
鼻咽癌%桥粒钙黏蛋白质类%DNA甲基化
鼻嚥癌%橋粒鈣黏蛋白質類%DNA甲基化
비인암%교립개점단백질류%DNA갑기화
nasopharyngeal neoplasms%desmosomal cadherins%DNA methylation
目的:探讨鼻咽癌组织和细胞E-钙黏蛋白( E-cadherin )基因表达水平与启动子甲基化的相关性,以及患者外周血E-cadherin甲基化作为肿瘤分子标志物的可能。方法采用RT-PCR检测鼻咽癌组织及两种鼻咽癌细胞株HNE1和CNE2中E-cadherin表达水平,以甲基化特异性PCR及硫化测序方法甲基化状态分析鼻咽癌组织、两种鼻咽癌细胞株及鼻咽癌患者外周血中E-cadherin启动子区域的甲基化状态。结果40例鼻咽癌组织中E-cadherin 表达下调率为80%(32/40),甲基化率为65%(26/40),5例正常鼻咽组织中未检测到E-cadherin甲基化,鼻咽癌患者外周血中E-cadherin甲基化率为45%(9/20)。结论基因启动子区域高甲基化状态可能是导致鼻咽癌组织中E-cadherin表达下调的重要机制,经外周血检测E-cadherin甲基化将为鼻咽癌的筛查诊断提供敏感、特异的无创检测方法。
目的:探討鼻嚥癌組織和細胞E-鈣黏蛋白( E-cadherin )基因錶達水平與啟動子甲基化的相關性,以及患者外週血E-cadherin甲基化作為腫瘤分子標誌物的可能。方法採用RT-PCR檢測鼻嚥癌組織及兩種鼻嚥癌細胞株HNE1和CNE2中E-cadherin錶達水平,以甲基化特異性PCR及硫化測序方法甲基化狀態分析鼻嚥癌組織、兩種鼻嚥癌細胞株及鼻嚥癌患者外週血中E-cadherin啟動子區域的甲基化狀態。結果40例鼻嚥癌組織中E-cadherin 錶達下調率為80%(32/40),甲基化率為65%(26/40),5例正常鼻嚥組織中未檢測到E-cadherin甲基化,鼻嚥癌患者外週血中E-cadherin甲基化率為45%(9/20)。結論基因啟動子區域高甲基化狀態可能是導緻鼻嚥癌組織中E-cadherin錶達下調的重要機製,經外週血檢測E-cadherin甲基化將為鼻嚥癌的篩查診斷提供敏感、特異的無創檢測方法。
목적:탐토비인암조직화세포E-개점단백( E-cadherin )기인표체수평여계동자갑기화적상관성,이급환자외주혈E-cadherin갑기화작위종류분자표지물적가능。방법채용RT-PCR검측비인암조직급량충비인암세포주HNE1화CNE2중E-cadherin표체수평,이갑기화특이성PCR급류화측서방법갑기화상태분석비인암조직、량충비인암세포주급비인암환자외주혈중E-cadherin계동자구역적갑기화상태。결과40례비인암조직중E-cadherin 표체하조솔위80%(32/40),갑기화솔위65%(26/40),5례정상비인조직중미검측도E-cadherin갑기화,비인암환자외주혈중E-cadherin갑기화솔위45%(9/20)。결론기인계동자구역고갑기화상태가능시도치비인암조직중E-cadherin표체하조적중요궤제,경외주혈검측E-cadherin갑기화장위비인암적사사진단제공민감、특이적무창검측방법。
Objective To investigate the expression and methylation status of E -cadherin in nasopharyngeal car-cinoma ( NPC) , and to evaluate efficacy of methylated E -cadherin in peripheral blood as a potential biomarker on the di-agnosis of NPC.Methods RT-PCR and methylation-specific PCR ( MSP) were performed to analyze the mRNA ex-pression levels and methylation status of E -cadherin in primary NPC specimens and two tumor cell lines .MSP was also used to observe the methylated E -cadherin in primary NPC specimens , two tumor cell lines and peripheral blood samples of NPC patients.Results Down-regulated E-cadherin expression was detected in 32 of 40 (80%) primary tumors as well as two NPC cell lines , when compared with normal tissues .Methylated E-cadherin was observed in 26 of 40 (65%) primary tumors but not in normal tissues .Moreover, E-cadherin methylation was also detected in 9 of 20 (45%) periph-eral blood samples of NPC patients .Conclusion Promoter methylation may be one of the mechanisms inducing E -cad-herin silencing .Detection of methylated E -cadherin in peripheral blood suggests potential clinical application for nonin -vasive diagnosis and disease monitoring of NPC .