Literature DB >> 21730103

Pancreatic ductal adenocarcinoma and acinar cells: a matter of differentiation and development?

Ilse Rooman1, Francisco X Real.   

Abstract

Pancreatic ductal adenocarcinoma (PDAC) has long been considered to arise from pancreatic ducts on the basis of its morphology, the occurrence of dysplasia in putative preneoplastic ductal lesions, and the absence of acinar dysplasia in the pancreas of patients with PDAC. However, evidence gathered through both in vitro studies and--more importantly--genetic mouse models of PDAC shows that ductal-type tumours can arise from acinar cells. These findings raise new important questions related to PDAC pathophysiology and call for in-depth studies of acinar cell differentiation in order to better understand PDAC biology. The authors review these issues and discuss how the novel findings should impact on future work aiming at early diagnosis and improved outcome of patients with PDAC.

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Year:  2011        PMID: 21730103     DOI: 10.1136/gut.2010.235804

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  46 in total

Review 1.  Differentiation and Inflammation: 'Best Enemies' in Gastrointestinal Carcinogenesis.

Authors:  Nathan M Krah; L Charles Murtaugh
Journal:  Trends Cancer       Date:  2016-12

2.  A new PDAC mouse model originated from iPSCs-converted pancreatic cancer stem cells (CSCcm).

Authors:  Anna Sanchez Calle; Neha Nair; Aung KoKo Oo; Marta Prieto-Vila; Megumi Koga; Apriliana Cahya Khayrani; Maram Hussein; Laura Hurley; Arun Vaidyanath; Akimasa Seno; Yoshiaki Iwasaki; Malu Calle; Tomonari Kasai; Masaharu Seno
Journal:  Am J Cancer Res       Date:  2016-12-01       Impact factor: 6.166

3.  Loss of a primary cilium in PDAC.

Authors:  Tetsuo Kobayashi; Hiroshi Itoh
Journal:  Cell Cycle       Date:  2017-03-20       Impact factor: 4.534

Review 4.  Acinar cell plasticity and development of pancreatic ductal adenocarcinoma.

Authors:  Peter Storz
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2017-03-08       Impact factor: 46.802

5.  Pancreatic Inflammation Redirects Acinar to β Cell Reprogramming.

Authors:  Hannah W Clayton; Anna B Osipovich; Jennifer S Stancill; Judsen D Schneider; Pedro G Vianna; Carolyn M Shanks; Weiping Yuan; Guoqiang Gu; Elisabetta Manduchi; Christian J Stoeckert; Mark A Magnuson
Journal:  Cell Rep       Date:  2016-11-15       Impact factor: 9.423

6.  KCa3.1 (IK) modulates pancreatic cancer cell migration, invasion and proliferation: anomalous effects on TRAM-34.

Authors:  B Bonito; D R P Sauter; A Schwab; M B A Djamgoz; I Novak
Journal:  Pflugers Arch       Date:  2016-10-17       Impact factor: 3.657

7.  Glucagon-Like Peptide-1 Receptor Expression in Normal and Neoplastic Human Pancreatic Tissues.

Authors:  Marco Dal Molin; Haeryoung Kim; Amanda Blackford; Rajni Sharma; Michael Goggins
Journal:  Pancreas       Date:  2016-04       Impact factor: 3.327

Review 8.  Phosphatidylinositol 3-Kinase: A Link Between Inflammation and Pancreatic Cancer.

Authors:  Chiara Birtolo; Vay Liang W Go; Andrzej Ptasznik; Guido Eibl; Stephen J Pandol
Journal:  Pancreas       Date:  2016-01       Impact factor: 3.327

9.  Aberrant expression of mucin core proteins and o-linked glycans associated with progression of pancreatic cancer.

Authors:  Neeley Remmers; Judy M Anderson; Erin M Linde; Dominick J DiMaio; Audrey J Lazenby; Hans H Wandall; Ulla Mandel; Henrik Clausen; Fang Yu; Michael A Hollingsworth
Journal:  Clin Cancer Res       Date:  2013-02-27       Impact factor: 12.531

10.  A Review of the Current Status and Concept of the Emerging Implications of Zinc and Zinc Transporters in the Development of Pancreatic Cancer.

Authors:  Leslie C Costello; Renty B Franklin
Journal:  Pancreat Disord Ther       Date:  2013
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