Losses at chromosome 4q are associated with poor survival in operable ductal pancreatic adenocarcinoma

Luebke, A. M. and Baudis, M. and Matthaei, H. and Vashist, Y. K. and Verde, P. E. and Hosch, S. B. and Erbersdobler, A. and Klein, C. A. and Izbicki, J. R. and Knoefel, W. T. and Stoecklein, N. H. (2012) Losses at chromosome 4q are associated with poor survival in operable ductal pancreatic adenocarcinoma. PANCREATOLOGY, 12 (1). pp. 16-22. ISSN 1424-3903,

Full text not available from this repository. (Request a copy)

Abstract

Here we tested the prognostic impact of genomic alterations in operable localized pancreatic ductal adenocarcinoma (PDAC). Fifty-two formalin-fixed and paraffin-embedded primary PDAC were laser micro-dissected and were investigated by comparative genomic hybridization after whole genome amplification using an adapter-linker PCR. Chromosomal gains and losses were correlated to clinicopathological parameters and clinical follow-up data. The most frequent aberration was loss on chromosome 17p (65%) while the most frequent gains were detected at 2q (41%) and 8q (41%), respectively. The concomitant occurrence of losses at 9p and 17p was found to be statistically significant. Higher rates of chromosomal losses were associated with a more advanced primary tumor stage and losses at 9p and 18q were significantly associated with presence of lymphatic metastasis (chi-square: p = 0.03, p = 0.05, respectively). Deletions on chromosome 4 were of prognostic significance for overall survival and tumor recurrence (Cox-multivariate analysis: p = 0.026 and p = 0.021, respectively). In conclusion our data suggest the common alterations at chromosome 8q, 9p, 17p and 18q as well as the prognostic relevant deletions on chromosome 4q as relevant for PDAC progression. Our comprehensive data from 52 PDAC should provide a basis for future studies with a higher resolution to discover the relevant genes located within the chromosomal aberrations identified. Copyright (C) 2012, IAP and EPC. Published by Elsevier India, a division of Reed Elsevier India Pvt. Ltd. All rights reserved.

Item Type: Article
Uncontrolled Keywords: COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER; PROGNOSTIC-SIGNIFICANCE; CANCER RELEVANCE; WIDE ANALYSIS; R1 RESECTION; PHASE-II; AMPLIFICATION; DNA; IDENTIFICATION; CGH; PDAC; Pancreatic cancer; 4q loss; Clinical follow-up; Prognosis
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für experimentelle Medizin und Therapieverfahren
Depositing User: Dr. Gernot Deinzer
Date Deposited: 25 May 2020 07:48
Last Modified: 25 May 2020 07:48
URI: https://pred.uni-regensburg.de/id/eprint/19534

Actions (login required)

View Item View Item