Literature DB >> 25216220

A clinicopathological and molecular analysis of 200 traditional serrated adenomas.

Mark L Bettington1, Neal I Walker2, Christophe Rosty3, Ian S Brown4, Andrew D Clouston5, Diane M McKeone6, Sally-Ann Pearson6, Kerenaftali Klein7, Barbara A Leggett8, Vicki L J Whitehall9.   

Abstract

The traditional serrated adenoma is the least common colorectal serrated polyp. The clinicopathological features and molecular drivers of these polyps require further investigation. We have prospectively collected a cohort of 200 ordinary and advanced traditional serrated adenomas and performed BRAF and KRAS mutational profiling, CpG island methylator phenotype analysis, and immunohistochemistry for a panel of 7 antibodies (MLH1, β-catenin, p53, p16, Ki67, CK7, and CK20) on all cases. The mean age of the patients was 64 years and 50% were female. Of the polyps, 71% were distal. Advanced histology (overt dysplasia or carcinoma) was present in 19% of cases. BRAF mutation was present in 67% and KRAS mutation in 22%. BRAF mutant traditional serrated adenomas were more frequently proximal (39% versus 2%; P≤0.0001), were exclusively associated with a precursor polyp (57% versus 0%; P≤0.0001), and were more frequently CpG island methylator phenotype high (60% versus 16%; P≤0.0001) than KRAS mutant traditional serrated adenomas. Advanced traditional serrated adenomas retained MLH1 expression in 97%, showed strong p53 staining in 55%, and nuclear β-catenin staining in 40%. P16 staining was lost in the advanced areas of 55% of BRAF mutant traditional serrated adenomas compared with 10% of the advanced areas of KRAS mutant or BRAF/KRAS wild-type traditional serrated adenomas. BRAF and KRAS mutant traditional serrated adenomas are morphologically related but biologically disparate polyps with distinctive clinicopathological and molecular features. The overwhelming majority of traditional serrated adenomas retain mismatch repair enzyme function indicating a microsatellite-stable phenotype. Malignant progression occurs via TP53 mutation and Wnt pathway activation regardless of mutation status. However, CDKN2A (encoding the p16 protein) is silenced nearly exclusively in the advanced areas of the BRAF mutant traditional serrated adenomas. Thus, the BRAF mutant traditional serrated adenoma represents an important precursor of the aggressive BRAF mutant, microsatellite-stable subtype of colorectal carcinoma.

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Year:  2014        PMID: 25216220     DOI: 10.1038/modpathol.2014.122

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  39 in total

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2.  Clinicopathologic and genetic characterization of traditional serrated adenomas of the colon.

Authors:  Baojin Fu; Shinichi Yachida; Richard Morgan; Yi Zhong; Elizabeth A Montgomery; Christine A Iacobuzio-Donahue
Journal:  Am J Clin Pathol       Date:  2012-09       Impact factor: 2.493

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4.  Up and downregulation of p16(Ink4a) expression in BRAF-mutated polyps/adenomas indicates a senescence barrier in the serrated route to colon cancer.

Authors:  Lydia Kriegl; Jens Neumann; Michael Vieth; Florian R Greten; Simone Reu; Andreas Jung; Thomas Kirchner
Journal:  Mod Pathol       Date:  2011-03-18       Impact factor: 7.842

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Authors:  Douglas K Rex; Dennis J Ahnen; John A Baron; Kenneth P Batts; Carol A Burke; Randall W Burt; John R Goldblum; José G Guillem; Charles J Kahi; Matthew F Kalady; Michael J O'Brien; Robert D Odze; Shuji Ogino; Susan Parry; Dale C Snover; Emina Emilia Torlakovic; Paul E Wise; Joanne Young; James Church
Journal:  Am J Gastroenterol       Date:  2012-06-19       Impact factor: 10.864

6.  CpG island methylator phenotype in colorectal cancer.

Authors:  M Toyota; N Ahuja; M Ohe-Toyota; J G Herman; S B Baylin; J P Issa
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Review 7.  Mixed hyperplastic adenomatous polyps/serrated adenomas. A distinct form of colorectal neoplasia.

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8.  Distinct CpG island methylation profiles and BRAF mutation status in serrated and adenomatous colorectal polyps.

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9.  Beta-catenin nuclear labeling is a common feature of sessile serrated adenomas and correlates with early neoplastic progression after BRAF activation.

Authors:  Shinichi Yachida; Shiyama Mudali; Sherri A Martin; Elizabeth A Montgomery; Christine A Iacobuzio-Donahue
Journal:  Am J Surg Pathol       Date:  2009-12       Impact factor: 6.394

10.  Morphologic reappraisal of serrated colorectal polyps.

Authors:  Emina Torlakovic; Eva Skovlund; Dale C Snover; Goran Torlakovic; Jahn M Nesland
Journal:  Am J Surg Pathol       Date:  2003-01       Impact factor: 6.394

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  44 in total

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2.  Volumetric growth rates of sessile serrated adenomas/polyps observed in situ at longitudinal CT colonography.

Authors:  P J Pickhardt; B D Pooler; K A Matkowskyj; D H Kim; W M Grady; R B Halberg
Journal:  Eur Radiol       Date:  2019-02-11       Impact factor: 5.315

3.  The role of APC in WNT pathway activation in serrated neoplasia.

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4.  Clinicopathological and molecular correlations in traditional serrated adenoma.

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5.  Gastric and small intestinal traditional serrated adenomas: a detailed morphologic and immunohistochemical analysis.

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Review 6.  Serrated neoplasia-role in colorectal carcinogenesis and clinical implications.

Authors:  Joep E G IJspeert; Louis Vermeulen; Gerrit A Meijer; Evelien Dekker
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2015-05-12       Impact factor: 46.802

Review 7.  Management of Serrated Polyps of the Colon.

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Journal:  Curr Treat Options Gastroenterol       Date:  2018-03

8.  Subtypes of the Type II Pit Pattern Reflect Distinct Molecular Subclasses in the Serrated Neoplastic Pathway.

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Journal:  Dig Dis Sci       Date:  2018-03-15       Impact factor: 3.199

9.  Biomarkers for the identification of precursor polyps of colorectal serrated adenocarcinomas.

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10.  Molecular Oncology in Management of Colorectal Cancer.

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