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Dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer

BACKGROUND AND AIM: Although high expression of Dickkopf‐4 (DKK‐4) in colorectal cancer has been reported in previous studies, its impact on clinicopathological features, including the prognosis and mechanism of expression, has not been well clarified to date. METHODS: (i) DKK‐4 protein expression w...

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Autores principales: Tsukui, Yuya, Yamaguchi, Tatsuya, Maekawa, Shinya, Takano, Shinichi, Sato, Tadashi, Enomoto, Nobuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788377/
https://www.ncbi.nlm.nih.gov/pubmed/31633047
http://dx.doi.org/10.1002/jgh3.12177
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author Tsukui, Yuya
Yamaguchi, Tatsuya
Maekawa, Shinya
Takano, Shinichi
Sato, Tadashi
Enomoto, Nobuyuki
author_facet Tsukui, Yuya
Yamaguchi, Tatsuya
Maekawa, Shinya
Takano, Shinichi
Sato, Tadashi
Enomoto, Nobuyuki
author_sort Tsukui, Yuya
collection PubMed
description BACKGROUND AND AIM: Although high expression of Dickkopf‐4 (DKK‐4) in colorectal cancer has been reported in previous studies, its impact on clinicopathological features, including the prognosis and mechanism of expression, has not been well clarified to date. METHODS: (i) DKK‐4 protein expression was analyzed by immunohistochemical staining with anti‐DKK‐4 antibody using archived formalin‐fixed paraffin‐embedded specimens obtained at surgery from 122 patients with colorectal cancer, and its association with clinicopathological findings was also investigated. (ii) The association between intratumoral DKK‐4 protein expression and somatic hotspot mutations in cancer‐associated genes in 40 patients was investigated using a next‐generation sequencer. RESULTS: In cross‐section, DKK‐4 protein expression in colorectal tissue was related to an adenocarcinoma of a histologically differentiated type (tub1/tub2, P = 0.032) and distant metastasis (P = 0.012). Longitudinally, however, DKK‐4 was not an independent prognostic factor determining overall survival (OS). On the other hand, in patients with metastasis, high DKK‐4 protein was independently associated with short OS (P = 0.013). In addition, colorectal cancer tissue with high DKK‐4 protein expression was associated with hotspot mutations in Wnt/β catenin‐signaling molecules (APC, CTNNB1, and FBXW7, P = 0.03). CONCLUSION: Intratumoral DKK‐4 expression, by partly reflecting the Wnt/β catenin pathway, is strongly associated with the advancement of colorectal cancer and OS in colorectal cancer patients with metastasis, although further studies are needed.
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spelling pubmed-67883772019-10-18 Dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer Tsukui, Yuya Yamaguchi, Tatsuya Maekawa, Shinya Takano, Shinichi Sato, Tadashi Enomoto, Nobuyuki JGH Open Original Articles BACKGROUND AND AIM: Although high expression of Dickkopf‐4 (DKK‐4) in colorectal cancer has been reported in previous studies, its impact on clinicopathological features, including the prognosis and mechanism of expression, has not been well clarified to date. METHODS: (i) DKK‐4 protein expression was analyzed by immunohistochemical staining with anti‐DKK‐4 antibody using archived formalin‐fixed paraffin‐embedded specimens obtained at surgery from 122 patients with colorectal cancer, and its association with clinicopathological findings was also investigated. (ii) The association between intratumoral DKK‐4 protein expression and somatic hotspot mutations in cancer‐associated genes in 40 patients was investigated using a next‐generation sequencer. RESULTS: In cross‐section, DKK‐4 protein expression in colorectal tissue was related to an adenocarcinoma of a histologically differentiated type (tub1/tub2, P = 0.032) and distant metastasis (P = 0.012). Longitudinally, however, DKK‐4 was not an independent prognostic factor determining overall survival (OS). On the other hand, in patients with metastasis, high DKK‐4 protein was independently associated with short OS (P = 0.013). In addition, colorectal cancer tissue with high DKK‐4 protein expression was associated with hotspot mutations in Wnt/β catenin‐signaling molecules (APC, CTNNB1, and FBXW7, P = 0.03). CONCLUSION: Intratumoral DKK‐4 expression, by partly reflecting the Wnt/β catenin pathway, is strongly associated with the advancement of colorectal cancer and OS in colorectal cancer patients with metastasis, although further studies are needed. Wiley Publishing Asia Pty Ltd 2019-04-10 /pmc/articles/PMC6788377/ /pubmed/31633047 http://dx.doi.org/10.1002/jgh3.12177 Text en © 2019 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Tsukui, Yuya
Yamaguchi, Tatsuya
Maekawa, Shinya
Takano, Shinichi
Sato, Tadashi
Enomoto, Nobuyuki
Dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer
title Dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer
title_full Dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer
title_fullStr Dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer
title_full_unstemmed Dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer
title_short Dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer
title_sort dickkopf‐4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788377/
https://www.ncbi.nlm.nih.gov/pubmed/31633047
http://dx.doi.org/10.1002/jgh3.12177
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