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Differences in gene expression despite identical histomorphology in sinonasal intestinal‐type adenocarcinoma and metastases from colorectal adenocarcinoma

Authors :
Sannia Sjöstedt
Filipe Garrett Vieira
Kirstine Karnov
Tina Klitmøller Agander
Gro Linno Willemoe
Kristoffer Staal Rohrberg
Finn Cilius Nielsen
Christian von Buchwald
Source :
Sjöstedt, S, Vieira, F G, Karnov, K, Agander, T K, Willemoe, G L, Rohrberg, K S, Nielsen, F C & von Buchwald, C 2022, ' Differences in gene expression despite identical histomorphology in sinonasal intestinal-type adenocarcinoma and metastases from colorectal adenocarcinoma ', APMIS, vol. 130, no. 9, pp. 551-559 . https://doi.org/10.1111/apm.13252
Publication Year :
2022
Publisher :
Wiley, 2022.

Abstract

Sinonasal intestinal-type adenocarcinoma (sITAC) is histomorphologically indistinguishable from colorectal adenocarcinoma (CRC) leading to diagnostic challenges. Metastases from CRCs to the sinonasal tract have been reported. The aim of the study was to identify a biomarker making it possible to distinguish between sITAC and metastases of colorectal origin. Formalin-fixated paraffin-embedded (FFPE) tissue from 20 consecutive patients with sITAC treated at Rigshospitalet, Denmark from 2005 to 2017, 20 patients with CRC, and second patients with both sinonasal and colorectal carcinomas were included, and RNA-sequencing was performed on all samples. Moreover, a series of 26 samples from metastasizing CRC were included (in-house data). 3139 differentially expressed genes were identified, of these several were deemed as possible biomarkers, including CSDE1, for which immunohistochemical staining was performed. sITAC and CRC differ in genomic expression. CSDE1, previously found upregulated in CRC, was significantly differentially expressed. Using immunohistochemical staining, no sITACs displayed strong and diffuse staining for CSDE1, which represents a potential marker to use in distinguishing sITAC from a metastasis of colorectal origin. This knowledge could improve the diagnostic process and hopefully the outcome in patients with this rare tumor.

Details

ISSN :
16000463 and 09034641
Volume :
130
Database :
OpenAIRE
Journal :
APMIS
Accession number :
edsair.doi.dedup.....f41f6592d2ee1e8bdcdcb3584574f4ee
Full Text :
https://doi.org/10.1111/apm.13252