z-logo
open-access-imgOpen Access
Investigation of Archived Formalin-Fixed Paraffin-Embedded Pancreatic Tissue with Whole-Genome Gene Expression Microarray
Author(s) -
Nete Vinstrup Michelsen,
Klaus Brusgaard,
Qihua Tan,
Mads Thomassen,
Khalid Hussain,
Henrik Thybo Christesen
Publication year - 2011
Publication title -
isrn pathology
Language(s) - English
Resource type - Journals
eISSN - 2090-570X
pISSN - 2090-5718
DOI - 10.5402/2011/275102
Subject(s) - biology , gene , pancreatic cancer , gene expression , pancreas , microarray , tissue microarray , computational biology , pathology , bioinformatics , cancer , genetics , medicine , endocrinology
The use of formalin-fixed, paraffin-embedded (FFPE) tissue overcomes the most prominent issues related to research on relatively rare diseases: limited sample size, availability of control tissue, and time frame. The use of FFPE pancreatic tissue in GEM may be especially challenging due to its very high amounts of ribonucleases compared to other tissues/organs. In choosing pancreatic tissue, we therefore indirectly address the applicability of other FFPE tissues to gene expression microarray (GEM). GEM was performed on archived, routinely fixed, FFPE pancreatic tissue from patients with congenital hyperinsulinism (CHI), insulinoma, and deceased age-appropriate neonates, using whole-genome arrays. Although ribonuclease-rich, we obtained biologically relevant and disease-specific, significant genes; cancer-related genes; genes involved in (a) the regulation of insulin secretion and synthesis, (b) amino acid metabolism, and (c) calcium ion homeostasis. These results should encourage future research and GEM studies on FFPE tissue from the invaluable biobanks available at the departments of pathology worldwide.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom