Gene expression changes associated with the progression of intraductal papillary mucinous neoplasms
- PMID: 22273699
- DOI: 10.1097/MPA.0b013e31823d7b36
Gene expression changes associated with the progression of intraductal papillary mucinous neoplasms
Abstract
Objectives: The diagnosis of high-grade intraductal papillary mucinous neoplasm (IPMN) is difficult to distinguish from low-grade IPMN. The aim of this study was to identify potential markers for the discrimination of high-grade and invasive (HgInv) IPMN from low- and moderate-grade dysplasia IPMN.
Methods: Laser capture microdissection was used to isolate distinct foci of low-grade, moderate-grade, high-grade, and invasive IPMN from paraffin-embedded archival tissue from 14 patients who underwent resection for IPMN. Most samples included multiple grades in the same specimen. Affymetrix Human Exon microarrays were used to compare low- and moderate-grade dysplasia IPMN with HgInv IPMN.
Results: Sixty-two genes were identified as showing significant changes in expression (P ≤ 0.05 and a 2-fold cutoff), including up-regulation of 41 in HgInv IPMN. Changes in gene expression are associated with biological processes related to malignant behavior including cell motion, cell proliferation, response to hypoxia, and epithelial-to-mesenchymal transition. In addition, altered signaling in several transforming growth factor β-related pathways was exhibited in the progression of IPMN to malignancy.
Conclusions: This study identifies a set of genes associated with the progression of IPMN to malignancy. These genes are potential markers that could be used to identify IPMN requiring surgical resection.
Similar articles
-
Intraductal papillary mucinous neoplasm.Hum Pathol. 2012 Jan;43(1):1-16. doi: 10.1016/j.humpath.2011.04.003. Epub 2011 Jul 20. Hum Pathol. 2012. PMID: 21777948
-
Proteomic assessment of markers for malignancy in the mucus of intraductal papillary mucinous neoplasms of the pancreas.Pancreas. 2012 Mar;41(2):169-74. doi: 10.1097/MPA.0b013e3182289356. Pancreas. 2012. PMID: 22076567
-
Epithelial-to-mesenchymal transition (EMT) in intraductal papillary mucinous neoplasm (IPMN) is associated with high tumor grade and adverse outcomes.Ann Surg Oncol. 2014 Dec;21 Suppl 4:S750-7. doi: 10.1245/s10434-014-3946-5. Epub 2014 Jul 29. Ann Surg Oncol. 2014. PMID: 25069861
-
Epigenetic alterations in intraductal papillary mucinous neoplasms of the pancreas.J Hepatobiliary Pancreat Surg. 2006;13(4):280-5. doi: 10.1007/s00534-005-1056-2. J Hepatobiliary Pancreat Surg. 2006. PMID: 16858538 Review.
-
Molecular genetics of intraductal papillary-mucinous neoplasms of the pancreas.J Hepatobiliary Pancreat Surg. 2007;14(3):233-7. doi: 10.1007/s00534-006-1167-4. Epub 2007 May 29. J Hepatobiliary Pancreat Surg. 2007. PMID: 17520197 Review.
Cited by
-
Follow, consider, and catch: second primary tumors in acromegaly patients.Endocrine. 2023 Apr;80(1):160-173. doi: 10.1007/s12020-022-03282-7. Epub 2022 Dec 15. Endocrine. 2023. PMID: 36517649
-
Molecular characterization of organoids derived from pancreatic intraductal papillary mucinous neoplasms.J Pathol. 2020 Nov;252(3):252-262. doi: 10.1002/path.5515. Epub 2020 Sep 19. J Pathol. 2020. PMID: 32696980 Free PMC article.
-
Prognostic significance of E-cadherin and ZEB1 expression in intraductal papillary mucinous neoplasm.Oncotarget. 2017 Dec 7;9(1):306-320. doi: 10.18632/oncotarget.23012. eCollection 2018 Jan 2. Oncotarget. 2017. PMID: 29416615 Free PMC article.
-
The Role of Genetic, Metabolic, Inflammatory, and Immunologic Mediators in the Progression of Intraductal Papillary Mucinous Neoplasms to Pancreatic Adenocarcinoma.Cancers (Basel). 2023 Mar 11;15(6):1722. doi: 10.3390/cancers15061722. Cancers (Basel). 2023. PMID: 36980608 Free PMC article. Review.
-
Identification of key lncRNAs in the tumorigenesis of intraductal pancreatic mucinous neoplasm by coexpression network analysis.Cancer Med. 2020 Jun;9(11):3840-3851. doi: 10.1002/cam4.2927. Epub 2020 Apr 2. Cancer Med. 2020. PMID: 32239802 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases