Abdel-Latif Mohamed M M, O'Riordan James, Windle Henry J, Carton Eleanor, Ravi Nagunivan, Kelleher Dermot, Reynolds John V
Department of Clinical Surgery, Trinity Centre for Health Sciences, St. James's Hospital and Trinity College Dublin, Dublin 8, Ireland.
Ann Surg. 2004 Apr;239(4):491-500. doi: 10.1097/01.sla.0000118751.95179.c6.
To examine the expression of the transcription factor nuclear factor kappa B (NF-kappaB) in Barrett's epithelium and adenocarcinoma and the impact of NF-kappaB expression on tumor stage and response to neoadjuvant chemotherapy and radiation therapy.
Progression of Barrett's esophagus to adenocarcinoma is associated with a wide range of cellular and molecular abnormalities. Nuclear factor-kappa B (NF-kappaB) regulates several genes involved in inflammatory, immune and apoptotic responses, but its role in esophageal inflammation and tumorigenesis has not been reported.
Mobility shift assay was used to measure NF-kappaB activity in nuclear extracts of fresh-frozen biopsies from tumor and uninvolved tissues (n = 30) and esophageal cell lines OE33, SKGT-4, and OE21. RelA expression was assessed by immunohistochemical staining (n = 97). The NF-kappaB/RelA and IkappaB protein expressions were also examined by Western blotting.
NF-kappaB was not expressed in normal esophageal squamous epithelium, in contrast to increased expression in 40% of patients with Barrett's epithelium. Sixty-one percent of resected tumors (n = 97) displayed NF-kappaB immunoreactivity, and 87.5% of the NF-kappaB-positive tumors were Stage IIb and III compared with only 12.5% of patients with Stage I and IIa disease (P < 0.05). The expression of NF-kappaB inversely correlated with major or complete pathologic responses to neoadjuvant chemotherapy and radiation therapy, with 15/20 (75%) responders in the NF-kappaB-negative group compared with 7/38 (18%) in the NF-kappaB-positive group (P < 0.00001). Moreover, incubation of esophageal cell lines OE33, SKGT-4, and OE21 with deoxycholic acid or low pH induced NF-kappaB expression.
Bile acids and low pH induce NF-kappaB expression in esophageal cell lines. NF-kappaB activation is common in esophageal adenocarcinoma. In patients with Barrett's epithelium and an associated esophageal adenocarcinoma, there is a progressive expression of NF-kappaB through Barrett's tumorigenesis. The absence of NF-kappaB expression in esophageal adenocarcinoma correlates with response to neoadjuvant chemoradiotherapy and may be of value in predicting response to neoadjuvant therapy.
检测转录因子核因子κB(NF-κB)在巴雷特食管上皮及腺癌中的表达情况,以及NF-κB表达对肿瘤分期、新辅助化疗和放疗反应的影响。
巴雷特食管进展为腺癌与多种细胞和分子异常有关。核因子κB(NF-κB)调控多个参与炎症、免疫和凋亡反应的基因,但其在食管炎症和肿瘤发生中的作用尚未见报道。
采用凝胶迁移试验检测新鲜冷冻活检肿瘤组织及未受累组织(n = 30)以及食管癌细胞系OE33、SKGT-4和OE21细胞核提取物中的NF-κB活性。通过免疫组织化学染色评估RelA表达(n = 97)。还通过蛋白质印迹法检测NF-κB/RelA和IκB蛋白表达。
正常食管鳞状上皮中未检测到NF-κB表达,相比之下,40%的巴雷特食管上皮患者表达增加。61%的切除肿瘤(n = 97)显示NF-κB免疫反应性,87.5%的NF-κB阳性肿瘤为Ⅱb期和Ⅲ期,而Ⅰ期和Ⅱa期疾病患者仅占12.5%(P < 0.05)。NF-κB的表达与新辅助化疗和放疗的主要或完全病理反应呈负相关,NF-κB阴性组20例中有15例(75%)有反应,而NF-κB阳性组38例中有7例(18%)有反应(P < 0.00001)。此外,用脱氧胆酸或低pH值处理食管癌细胞系OE33、SKGT-4和OE21可诱导NF-κB表达。
胆汁酸和低pH值可诱导食管癌细胞系中NF-κB表达。NF-κB激活在食管腺癌中常见。在巴雷特食管上皮及相关食管腺癌患者中,NF-κB在巴雷特肿瘤发生过程中呈渐进性表达。食管腺癌中NF-κB表达缺失与新辅助放化疗反应相关,可能对预测新辅助治疗反应有价值。