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      Pancreatic undifferentiated carcinoma with osteoclast-like giant cells is genetically similar to, but clinically distinct from, conventional ductal adenocarcinoma

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          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.

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          Author and article information

          Journal
          0204634
          5121
          J Pathol
          J. Pathol.
          The Journal of pathology
          0022-3417
          1096-9896
          9 July 2019
          05 September 2017
          October 2017
          30 July 2019
          : 243
          : 2
          : 148-154
          Affiliations
          [1 ]Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy
          [2 ]Department of Pathology, Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins University School of Medicine, Baltimore, MD, USA
          [3 ]Department of Surgery, University and Hospital Trust of Verona, Verona, Italy
          [4 ]Department of Surgery, Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins University School of Medicine, Baltimore, MD, USA
          [5 ]ARC-Net Research Center, University of Verona, Verona, Italy
          [6 ]National Research Council, Neuroscience Institute, Aging Branch, Padua, Italy
          [7 ]Institute for Clinical Research and Education in Medicine (IREM), Padua, Italy
          [8 ]Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands
          [9 ]Department of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands
          [10 ]Sacro Cuore Don Calabria Hospital, Negrar, Verona, Italy
          [11 ]Department of Oncology, Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins University School of Medicine, Baltimore, MD, USA
          Author notes

          Author contributions statement

          CL and LDW designed the study. CL, LAAB, PC, GZ, AS, and LDW performed pathological review. CL, AP, GL, PC, RY, GR, and PP carried out experiments. CL, AP, AM, AN, NV, MN, RL, YN, IC, and GM analyzed data. CL, LAAB, GJAO, AS, and LDW interpreted data. CL and LDW wrote the paper. All authors had final approval of the submitted manuscript.

          [* ]Correspondence to: Laura D Wood, MD, PhD, CRB2 Room 345, 1550 Orleans Street, Baltimore, MD 21231, USA. ldwood@ 123456jhmi.edu Or Aldo Scarpa, MD, PhD, ARC-Net Centre for Applied Research on Cancer, Department of Diagnostics and Public Health, University and Hospital Trust of Verona, 37134 Verona, Italy. aldo.scarpa@ 123456univr.it
          Author information
          http://orcid.org/0000-0003-4901-4908
          http://orcid.org/0000-0003-3096-652X
          Article
          PMC6664430 PMC6664430 6664430 nihpa1037658
          10.1002/path.4941
          6664430
          28722124
          af3260c7-e223-4304-bcfc-b466c49cedd4
          History
          Categories
          Article

          whole exome sequencing,PDAC variants,undifferentiated carcinoma with osteoclast-like giant cells

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