Premium
Gene expression profiling of serrated polyps identifies annexin A10 as a marker of a sessile serrated adenoma/polyp
Author(s) -
Gonzalo David Hernandez,
Lai Keith K,
Shadrach Bonnie,
Goldblum John R,
Bennett Ana E,
DownsKelly Erinn,
Liu Xiuli,
Henricks Walter,
Patil Deepa T,
Carver Paula,
Na Jie,
Gopalan Banu,
Rybicki Lisa,
Pai Rish K
Publication year - 2013
Publication title -
the journal of pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.964
H-Index - 184
eISSN - 1096-9896
pISSN - 0022-3417
DOI - 10.1002/path.4200
Subject(s) - hyperplastic polyp , immunohistochemistry , colorectal cancer , pathology , microsatellite instability , gene expression profiling , gene expression , microbiology and biotechnology , gene , real time polymerase chain reaction , biology , medicine , cancer , genetics , colonoscopy , microsatellite , allele
Sessile serrated adenomas/polyps ( SSA /Ps) are precursors of colon cancer, particularly those that exhibit microsatellite instability. Distinguishing SSA /Ps from the related, but innocuous, microvesicular hyperplastic polyp ( MVHP ) can be challenging. In this study seven gastrointestinal pathologists reviewed 109 serrated polyps and identified 60 polyps with histological consensus. Microarray analysis was performed on six distal consensus MVHPs < 9 mm, six proximal consensus SSA /Ps > 9 mm, and six normal colon biopsies (three proximal, three distal). Comparative gene expression analysis confirmed the close relationship between SSA /Ps and MVHPs as there was overlapping expression of many genes. However, the gene expression profile in SSA /Ps had stronger and more numerous associations with cancer‐related genes compared with MVHPs . Three genes ( TFF2 , FABP6 , and ANXA10 ) were identified as candidates whose expression can differentiate SSA /Ps from MVHPs , and the differences in expression were confirmed by quantitative RT‐PCR . As ANXA10 showed the most promise in differentiating these polyps, the expression of ANXA10 was evaluated by immunohistochemistry in consensus SSA /Ps ( n = 26), MVHPs ( n = 21), and normal colon ( n = 9). Immunohistochemical expression of ANXA10 was not identified in separate samples of normal colon or in the normal colonic epithelium adjacent to the serrated polyps. Consistent with the microarray and quantitative RT‐PCR experiments, immunohistochemical expression of ANXA10 was markedly increased in SSA /Ps compared to MVHPs ( p < 0.0001). An ANXA10 score ≥ 3 has a sensitivity of 73% and a specificity of 95% in the diagnosis of an SSA /P. In conclusion, we show that SSA /Ps and MVHPs have significant overlap in gene expression, but also important differences, particularly in cancer‐related pathways. Expression of ANXA10 may be a potential marker of the serrated pathway to colon cancer. Copyright © 2013 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom