ANO1 protein as a potential biomarker for esophageal cancer prognosis and precancerous lesion development prediction

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 t...

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Published inOncotarget Vol. 7; no. 17; pp. 24374 - 24382
Main Authors 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
Format Journal Article
LanguageEnglish
Published United States 26.04.2016
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Abstract 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.
AbstractList 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.
OBJECTIVESAnoctamin 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.RESULTSANO1 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.METHODSImmunohistochemistry (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.CONCLUSIONSPositive ANO1 is a promising biomarker to predict the unfavorable outcome for ESCC patients. More importantly, it can predict disease progression of precancerous lesions.
Author Li, Min
Li, En-Min
Jia, Xue-Mei
Zhan, Qi-Min
He, Jian-Zhong
Zhang, Yu
Wei, Wen-Qiang
Wu, Li-Fei
Shi, Zhi-Zhou
Xu, Xin
Zhang, Tong-Tong
Shang, Li
Zhao, Xue-Ke
Wang, Li-Dong
Shi, Feng
Yang, Hai
Hao, Jia-Jie
Cai, Yan
Liu, Yi-Zhen
Wang, Ming-Rong
Liu, Hui-Juan
Jiang, Yan-Yi
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Keywords ANO1
esophageal squamous cell carcinoma
biomarker
prognosis
precancerous lesions
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References 22564524 - Cancer Res. 2012 Jul 1;72(13):3270-81
20571340 - Appl Immunohistochem Mol Morphol. 2010 Jul;18(4):333-7
24119907 - Zhonghua Zhong Liu Za Zhi. 2013 Jun;35(6):456-8
21296855 - CA Cancer J Clin. 2011 Mar-Apr;61(2):69-90
18981721 - Cancer Biol Ther. 2009 Jan;8(1):36-46
24009147 - Clin Cancer Res. 2013 Nov 1;19(21):5867-78
21705456 - Gut. 2011 Nov;60(11):1449-72
14657432 - N Engl J Med. 2003 Dec 4;349(23):2241-52
15111177 - Ann Thorac Surg. 2004 May;77(5):1740-4
22335248 - Histopathology. 2012 Jun;60(7):1099-106
19004025 - Int J Cancer. 2009 Feb 1;124(3):578-88
22912841 - PLoS One. 2012;7(8):e43265
19606013 - Am J Surg Pathol. 2009 Sep;33(9):1401-8
23431153 - Proc Natl Acad Sci U S A. 2013 Mar 12;110(11):E1026-34
24450308 - Mol Pain. 2014 Jan 23;10:5
24823391 - Endocrinology. 2014 Aug;155(8):2787-96
15215166 - Am J Pathol. 2004 Jul;165(1):107-13
18223323 - Am J Surg Pathol. 2008 Feb;32(2):210-8
22699056 - Nan Fang Yi Ke Da Xue Xue Bao. 2012 Jun;32(6):794-7
20664600 - Br J Cancer. 2010 Aug 24;103(5):715-26
22820160 - Cancer Lett. 2012 Dec 29;326(1):41-51
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Snippet Anoctamin 1 (ANO1) has been found to be overexpressed in esophageal squamous cell carcinoma (ESCC) in our previous study. Herein we showed the clinical...
OBJECTIVESAnoctamin 1 (ANO1) has been found to be overexpressed in esophageal squamous cell carcinoma (ESCC) in our previous study. Herein we showed the...
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SubjectTerms Anoctamin-1 - biosynthesis
Biomarkers, Tumor - metabolism
Carcinoma, Squamous Cell - diagnosis
Carcinoma, Squamous Cell - metabolism
Disease Progression
Esophageal Neoplasms - diagnosis
Esophageal Neoplasms - metabolism
Esophagus - metabolism
Esophagus - pathology
Female
Humans
Immunohistochemistry
Kaplan-Meier Estimate
Male
Middle Aged
Neoplasm Proteins - biosynthesis
Precancerous Conditions - diagnosis
Precancerous Conditions - metabolism
Prognosis
Title ANO1 protein as a potential biomarker for esophageal cancer prognosis and precancerous lesion development prediction
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