| Literature DB >> 28722124 |
Claudio Luchini1,2, Antonio Pea3,4, Gemma Lionheart2, Andrea Mafficini5, Alessia Nottegar1, Nicola Veronese6,7, Peter Chianchiano2, Lodewijk Aa Brosens8,9, Michaël Noë2,8, G Johan A Offerhaus8, Raluca Yonescu2, Yi Ning2, Giuseppe Malleo3, Giulio Riva1, Paola Piccoli1, Ivana Cataldo1, Paola Capelli1, Giuseppe Zamboni1,10, Aldo Scarpa1,5, Laura D Wood2,11.
Abstract
Undifferentiated carcinoma of the pancreas with osteoclast-like giant cells (UCOGC) is currently considered a morphologically and clinically distinct variant of pancreatic ductal adenocarcinoma (PDAC). In this study, we report clinical and pathological features of a series of 22 UCOGCs, including the whole exome sequencing of eight UCOGCs. We observed that 60% of the UCOGCs contained a well-defined epithelial component and that patients with pure UCOGC had a significantly better prognosis than did those with an UCOGC with an associated epithelial neoplasm. The genetic alterations in UCOGC are strikingly similar to those known to drive conventional PDAC, including activating mutations in the oncogene KRAS and inactivating mutations in the tumor suppressor genes CDKN2A, TP53, and SMAD4. These results further support the classification of UCOGC as a PDAC variant and suggest that somatic mutations are not the determinants of the unique phenotype of UCOGC.Entities:
Keywords: PDAC variants; undifferentiated carcinoma with osteoclast-like giant cells; whole exome sequencing
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Year: 2017 PMID: 28722124 PMCID: PMC6664430 DOI: 10.1002/path.4941
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 7.996