Identification of clinically-informative biomarkers for risk stratification within the spectrum of gastro-esophageal reflux disease in the South African population

C. Rensburg, J. D. Villiers, C. Daniels, Wright Ca, M. Kidd, G. Jong, M. Kotze
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Abstract

Background : Barrett's esophagus is the precursor of esophageal adenocarcinoma with a 5-year survival rate of 25-30%. Objective : To define clinically useful biomarkers for transcriptional profiling in South African patients with Barrett's esophagus in order to identify those patients with an increased cancer risk necessitating intensified surveillance intervals. Materials and method : One-hundred and two patients were recruited for the study. COX-2, c-myb and c-myc mRNA expression were measured using a quantitative PCR method in endoscopically obtained specimens of Barrett's metaplasia (BM, n=26) or dysplasia (BD, n=14) and matching squamous esophageal tissue (n=40), squamous esophageal tissue of patients with erosive esophagitis (n=20), non-erosive esophagitis (n=20) and normal controls (n=20). Two patients with Barrett's adenocarcinoma (BAC) were also studied. Results : Demographic data of the groups were comparable. No significant differences in m-RNA expression levels were observed between ethnic groups for the genes analyzed. In the BD/BAC group 69% (11/16) showed increased c-myb m-RNA expression compared with 35% (9/26) in the BM group (p = 0.03). In the BD patients 19% (3/16) had increased c-myc m-RNA expression compared to none in those with BM and BAC. One patient each with BM and BAC had increased COX-2 m-RNA levels. No significant associations were observed for COX-2 in any of the other study groups. Conclusion : In the South African study cohort c-myb appears to be a clinically useful molecular marker for Barrett's esophagus and increased cancer risk, since m-RNA levels are progressively more over expressed in the metaplasia-dysplasia-adenocarcinoma sequence. Further studies are required to clarify the potential significance c-myc and COX-2 in South African patients with Barrett's esophagus. South African Gastroenterology Review Vol. 3(1) 2005: 5-9
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鉴定南非人群胃食管反流疾病谱系内风险分层的临床信息生物标志物
背景:Barrett食管是食管腺癌的前体,5年生存率为25-30%。目的:为南非巴雷特食管患者的转录谱定义临床有用的生物标志物,以确定那些癌症风险增加、需要加强监测间隔的患者。材料与方法:本研究共招募了102例患者。采用定量PCR方法检测内镜下Barrett化生(BM, n=26)或不典型增生(BD, n=14)及匹配的食管鳞状组织(n=40)、糜烂性食管炎(n=20)、非糜烂性食管炎(n=20)和正常对照(n=20)标本中COX-2、c-myb和c-myc mRNA的表达。同时对2例巴雷特腺癌(BAC)患者进行了研究。结果:两组人口统计学资料具有可比性。所分析基因的m-RNA表达水平在不同种族间无显著差异。在BD/BAC组中,69%(11/16)的c-myb m-RNA表达增加,而BM组为35% (9/26)(p = 0.03)。在BD患者中,19%(3/16)的c-myc m-RNA表达升高,而在BM和BAC患者中没有升高。BM和BAC各有1例患者COX-2 m-RNA水平升高。在其他研究组中未观察到COX-2的显著相关性。结论:在南非的研究队列中,c-myb似乎是临床上有用的Barrett食管和癌症风险增加的分子标志物,因为m-RNA水平在化生-发育不良-腺癌序列中逐渐过度表达。需要进一步的研究来阐明c-myc和COX-2在南非Barrett食管患者中的潜在意义。南非胃肠病学评论Vol. 3(1) 2005: 5-9
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South African Gastroenterology Review
South African Gastroenterology Review Medicine-Gastroenterology
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