4.3 Article

A correlation of the endoscopic characteristics of colonic laterally spreading tumours with genetic alterations

Journal

EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
Volume 25, Issue 3, Pages 319-326

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MEG.0b013e32835b57e7

Keywords

adenomas; colonoscopy; colorectal neoplasms; laterally spreading tumours

Funding

  1. Cancer Institute New South Wales Early Career Development Fellowship
  2. Cancer Council New South Wales

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Objectives Laterally spreading tumours (LSTs) are a heterogeneous group of adenomas that are emerging as important precursors of colorectal cancer and in which the risk for cancer is related to their endoscopically definable morphology. It is currently unclear whether different molecular alterations determine their morphologies. We aimed to assess this relationship in LSTs using strict morphological classifications. Methods We characterized 135 sessile adenomatous lesions (>= 20 mm) according to histopathology and the Paris classification. We investigated key molecular changes commonly found in colorectal neoplasms, namely mutation of KRAS, BRAF, APC and CTNNB1 and microsatellite instability, and determined their relationship with morphology. Results The Paris classification revealed a heterogeneous cohort comprising Is/IIa + Is (41.5%), IIa/IIb (53.3%) and IIc/IIa + IIc (5.2%) lesions. Histopathological analysis showed that 19 (14.1%) of these were sessile serrated adenomas. Here, we defined a group of 58 lesions that showed either Paris IIa or IIb morphology with no serrated histopathology. These 'classical LSTs' showed the following molecular characteristics: microsatellite instability 0/56 (0%), APC mutation 29/30 (96.7%), CTNNB1 mutation 2/55 (3.6%), KRAS mutation 24/55 (43.6%) and BRAF mutation 2/55 (3.6%). Separation of lesions according to surface morphology showed that KRAS mutations occurred much more frequently in granular (56.4%, 22/39) than in nongranular LSTs (12.5%, 1/16, P=0.004). Conclusion The microsatellite instable pathway is not important in the development of LSTs, which are instead likely to develop along a divergent chromosomal instability pathway. We demonstrate the biological significance of endoscopic findings by showing that the morphological characteristics of LSTs are underpinned by distinctive molecular profiles. Eur J Gastroenterol Hepatol 25:319-326 (C) 2013 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.

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