Chromosomal imbalances in wood dust-related adenocarcinomas of the inner nose and their associations with pathological parameters

• Published in: The Journal of pathology 2005-10, Vol.207 (2), p.207-215
• Main Authors: Korinth, Dirk, Pacyna-Gengelbach, Manuela, Deutschmann, Nicole, Hattenberger, Sigurd, Bockmühl, Ulrike, Dietel, Manfred, Schroeder, Heinz-Georg, Donhuijsen, Konrad, Petersen, Iver
• Format: Article
• Language: English
• Subjects: adenocarcinoma; Adenocarcinoma - etiology; Adenocarcinoma - genetics; Adenocarcinoma - pathology; Adenocarcinoma, Bronchiolo-Alveolar - etiology; Adenocarcinoma, Bronchiolo-Alveolar - genetics; Adenocarcinoma, Bronchiolo-Alveolar - pathology; Adult; Aged; Aged, 80 and over; Biological and medical sciences; Carcinoma, Signet Ring Cell - etiology; Carcinoma, Signet Ring Cell - genetics; Carcinoma, Signet Ring Cell - pathology; Cell Differentiation - physiology; CGH; Chromosome Aberrations; differentiation grade; DNA, Neoplasm - genetics; Dust; Humans; intestinal type; Investigative techniques, diagnostic techniques (general aspects); Kleinsasser/Schroeder classification; Male; Medical sciences; Middle Aged; Nucleic Acid Hybridization - methods; Occupational Diseases - etiology; Occupational Diseases - genetics; Occupational Diseases - pathology; Occupational Exposure - adverse effects; Paranasal Sinus Neoplasms - etiology; Paranasal Sinus Neoplasms - genetics; Paranasal Sinus Neoplasms - pathology; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques; Wood; wood dust
• ISSN: 0022-3417; 1096-9896
• DOI: 10.1002/path.1819

Comparative genomic hybridization (CGH) was used to screen 42 wood dust‐related sinonasal adenocarcinomas for chromosomal alterations. The tumour collection comprised 39 papillary‐tubular cylinder cell adenocarcinomas (PTCCs; six cases G1, 23 G2, and ten G3), two alveolar goblet cell adenocarcinomas (AGCs), and one signet ring cell adenocarcinoma (SRC), according to the Kleinsasser and Schroeder classification. Copy number changes were detected in 41 tumours (97.6%). The one carcinoma without imbalances was a PTCC‐G1. DNA gains were most frequently seen on chromosomes 12p (83%), 7q (74%), 8q (71%), and 20q (71%), 11q (61%), 22 (59%), and 1q (52%). Pronounced overrepresentations suggestive of high copy amplifications were detected on 8q (15 cases, 36%), 7q (six cases, 14%), 20q (five cases, 12%), 13q14 (three cases, 7%), 1q22, 5p, 12p and 20 (two cases, 5% each), and 2q24, 3q13, 3q22, 7p, 14q12, and 16q13 (one case, each 2%). Frequent chromosomal losses occurred at 5q (81%), 18q (76%), 4 (74%), 8p (61%), 9p (60%), 6q and 17p (52% each), and 3p, 13q, and 21 (50% each). There was a quantitative as well as a qualitative increase of alterations from PTCC‐G1 to PTCC‐G2 and finally PTCC‐G3, confirming the usefulness of histopathological grading. While PTCC‐G1 carried only a few alterations, namely gains on chromosomes 17 and 7 as well as losses of 4q and 13q, PTCC‐G2 already carried many of the above‐mentioned alterations, while PTCC‐G3 showed significantly more gains of 7q, 8q, and 12p, and losses of 8p and 17p. Additionally, the latter subgroup was particularly prone to carry pronounced DNA gains. These data provide further evidence for a recurrent pattern of chromosomal imbalances in sinonasal adenocarcinomas and highlight distinct aberrations that are associated with tumour differentiation and progression. Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.