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Gremlin1 expression associates with serrated pathway and favourable prognosis in colorectal cancer.

Authors :
Pelli A
Väyrynen JP
Klintrup K
Mäkelä J
Mäkinen MJ
Tuomisto A
Karttunen TJ
Source :
Histopathology [Histopathology] 2016 Nov; Vol. 69 (5), pp. 831-838. Date of Electronic Publication: 2016 Aug 02.
Publication Year :
2016

Abstract

Aims: Gremlin1 is a bone morphogenetic protein (BMP) antagonist with a suggested role in colorectal cancer (CRC) progression. We have analysed Gremlin1 protein expression in CRC and assessed its correlation with clinicopathological characteristics, including developmental pathway and prognosis.<br />Methods and Results: Material included a non-selected series of 148 surgically treated CRC cases. The tumour-node-metastasis (TNM) stage, histological grade and inflammatory infiltrate at the invasive margin were assessed, and tumours were classified to serrated or non-serrated types. Immunohistochemistry was conducted to evaluate Gremlin1 expression. Prognosis (60-month follow-up) was analysed by Kaplan-Meier methods and Cox regression analysis. Gremlin1 expression was detected in epithelial cells both in normal mucosa and in carcinomas. Abundant expression in carcinomas associated with low TNM stage (P = 0.044), low histological grade (P = 0.044), serrated histology (P = 0.033 or P = 0.053 depending on the classification cut-off) and intensive inflammatory infiltrate at the invasive margin (P = 0.044), and was a stage independent indicator of extended survival (P = 0.029).<br />Conclusions: Gremlin1 protein expression in CRC associates with low tumour stage and extended survival independently of tumour stage, suggesting that it represents a relevant prognostic indicator in CRC. High expression in carcinomas with serrated histology suggests a potential role for Gremlin1 in the serrated pathway of CRC.<br /> (© 2016 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2559
Volume :
69
Issue :
5
Database :
MEDLINE
Journal :
Histopathology
Publication Type :
Academic Journal
Accession number :
27257976
Full Text :
https://doi.org/10.1111/his.13006