Shang Li, Hao Jia-Jie, Zhao Xue-Ke, He Jian-Zhong, Shi Zhi-Zhou, Liu Hui-Juan, Wu Li-Fei, Jiang Yan-Yi, Shi Feng, Yang Hai, Zhang Yu, Liu Yi-Zhen, Zhang Tong-Tong, Xu Xin, Cai Yan, Jia Xue-Mei, Li Min, Zhan Qi-Min, Li En-Min, Wang Li-Dong, Wei Wen-Qiang, Wang Ming-Rong
State Key Laboratory of Molecular Oncology, Cancer Institute (Hospital), Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100021, China.
Henan Key Laboratory for Esophageal Cancer Research of the First Affiliated Hospital, Zhengzhou University, Zhengzhou 450000, China.
Oncotarget. 2016 Apr 26;7(17):24374-82. doi: 10.18632/oncotarget.8223.
Anoctamin 1 (ANO1) has been found to be overexpressed in esophageal squamous cell carcinoma (ESCC) in our previous study. Herein we showed the clinical relevance of ANO1 alterations with ESCC and esophageal precancerous lesion progression.
ANO1 was detected in 38.1% (109/286) and 25.4% (77/303) of tumors in the two cohorts, but in none of morphologically normal operative margin tissues. ANO1 expression was significantly associated with a shorter overall survival (OS), especially in patients with moderately differentiated and stage IIA tumors. In 499 iodine-unstained biopsies from the endoscopic screening cohort in 2005-2007, all the 72 pathologically normal epithelial mucosa presented negative immunostaining, whereas ANO1 expression was observed in 3/11 tumors and 5/231 intraepithelial lesions. 7/8 ANO1-positive cases had developed unfavorable outcomes revealed by endoscopic follow-up in 2012. Analysis of another independent cohort of 148 intraepithelial lesions further confirmed the correlation between ANO1 expression and progression of precancerous lesions. 3/4 intraepithelial lesions with ANO1 expression had developed ESCC within 4-9 years after the initial endoscopic examination.
Immunohistochemistry (IHC) was performed to examine ANO1 expression in surgical ESCC specimens and two independent cohorts of esophageal biopsies from endoscopic screening in high-incidence area of ESCC in northern China. Association between ANO1 expression, clinico-pathologic parameters, and the impact on overall survival was analyzed.
Positive ANO1 is a promising biomarker to predict the unfavorable outcome for ESCC patients. More importantly, it can predict disease progression of precancerous lesions.
在我们之前的研究中发现,anoctamin 1(ANO1)在食管鳞状细胞癌(ESCC)中过表达。在此,我们展示了ANO1改变与ESCC及食管癌前病变进展的临床相关性。
在两个队列中,分别有38.1%(109/286)和25.4%(77/303)的肿瘤检测到ANO1,但在形态学正常的手术切缘组织中均未检测到。ANO1表达与总生存期(OS)显著相关,尤其是在中分化和IIA期肿瘤患者中。在2005 - 2007年内镜筛查队列的共499例碘不着色活检标本中,所有72例病理正常的上皮黏膜免疫染色均为阴性,而在11例肿瘤和231例上皮内病变中观察到ANO1表达。2012年内镜随访显示,8例ANO1阳性病例中有7例出现不良结局。对另一个包含148例上皮内病变的独立队列进行分析,进一步证实了ANO1表达与癌前病变进展之间的相关性。4例有ANO1表达的上皮内病变中有3例在首次内镜检查后4 - 9年内发展为ESCC。
采用免疫组织化学(IHC)检测手术切除的ESCC标本以及来自中国北方ESCC高发地区内镜筛查的两个独立食管活检队列中ANO1的表达。分析ANO1表达与临床病理参数之间的关联以及对总生存期的影响。
ANO1阳性是预测ESCC患者不良结局的一个有前景的生物标志物。更重要的是,它可以预测癌前病变的疾病进展。