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Prognostic impact of CD44-positive cancer stem-like cells at the invasive front of gastric cancer

BACKGROUND: The invasive tumour front may provide prognostic information. We examined the relationship between the presence of cancer stem cells (CSCs) at the invasive tumour front and prognosis in gastric cancer (GC). METHODS: CD44 is a CSC marker; accordingly, CD44 standard (CD44s), CD44 variant-6...

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Autores principales: Kodama, Hirokazu, Murata, Satoshi, Ishida, Mitsuaki, Yamamoto, Hiroshi, Yamaguchi, Tsuyoshi, Kaida, Sachiko, Miyake, Tohru, Takebayashi, Katsushi, Kushima, Ryoji, Tani, Masaji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243989/
https://www.ncbi.nlm.nih.gov/pubmed/27931044
http://dx.doi.org/10.1038/bjc.2016.401
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author Kodama, Hirokazu
Murata, Satoshi
Ishida, Mitsuaki
Yamamoto, Hiroshi
Yamaguchi, Tsuyoshi
Kaida, Sachiko
Miyake, Tohru
Takebayashi, Katsushi
Kushima, Ryoji
Tani, Masaji
author_facet Kodama, Hirokazu
Murata, Satoshi
Ishida, Mitsuaki
Yamamoto, Hiroshi
Yamaguchi, Tsuyoshi
Kaida, Sachiko
Miyake, Tohru
Takebayashi, Katsushi
Kushima, Ryoji
Tani, Masaji
author_sort Kodama, Hirokazu
collection PubMed
description BACKGROUND: The invasive tumour front may provide prognostic information. We examined the relationship between the presence of cancer stem cells (CSCs) at the invasive tumour front and prognosis in gastric cancer (GC). METHODS: CD44 is a CSC marker; accordingly, CD44 standard (CD44s), CD44 variant-6 (CD44v6), and CD44 variant-9 (CD44v9) expression were examined in 123 resected primary GCs and the clinical significance of CSCs at the invasive tumour front was analysed. RESULTS: Thirteen (10.6%), 79 (64.2%), and 47 (38.2%) GCs were CD44s-, CD44v6-, and CD44v9-positive, respectively. Patients with CD44-positive expression at the invasive tumour front had significantly poorer disease-specific survival than those with negative expression (CD44s: P<0.00001, CD44v6: P=0.013, CD44v9: P=0.0002). CD44s expression at the invasive tumour front was an independent prognostic factor in resectable GC patients (hazard ratio=3.13; 95% confidence interval, 1.09–9.01; P=0.035) and was significantly associated with peritoneal (P<0.001), lymphatic (P<0.001), and haematogenous recurrences (P=0.008). In addition, the number of CD44 isoforms expressed in cancer cells at the invasive tumour front was associated with patient prognosis. No conventional clinicopathological factors were independently associated with CD44 expression at the invasive tumour front. CONCLUSIONS: CD44-positive cancer stem-like cells at the invasive tumour front indicate poor survival and can be a unique biological prognostic factor for GC.
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spelling pubmed-52439892018-01-17 Prognostic impact of CD44-positive cancer stem-like cells at the invasive front of gastric cancer Kodama, Hirokazu Murata, Satoshi Ishida, Mitsuaki Yamamoto, Hiroshi Yamaguchi, Tsuyoshi Kaida, Sachiko Miyake, Tohru Takebayashi, Katsushi Kushima, Ryoji Tani, Masaji Br J Cancer Molecular Diagnostics BACKGROUND: The invasive tumour front may provide prognostic information. We examined the relationship between the presence of cancer stem cells (CSCs) at the invasive tumour front and prognosis in gastric cancer (GC). METHODS: CD44 is a CSC marker; accordingly, CD44 standard (CD44s), CD44 variant-6 (CD44v6), and CD44 variant-9 (CD44v9) expression were examined in 123 resected primary GCs and the clinical significance of CSCs at the invasive tumour front was analysed. RESULTS: Thirteen (10.6%), 79 (64.2%), and 47 (38.2%) GCs were CD44s-, CD44v6-, and CD44v9-positive, respectively. Patients with CD44-positive expression at the invasive tumour front had significantly poorer disease-specific survival than those with negative expression (CD44s: P<0.00001, CD44v6: P=0.013, CD44v9: P=0.0002). CD44s expression at the invasive tumour front was an independent prognostic factor in resectable GC patients (hazard ratio=3.13; 95% confidence interval, 1.09–9.01; P=0.035) and was significantly associated with peritoneal (P<0.001), lymphatic (P<0.001), and haematogenous recurrences (P=0.008). In addition, the number of CD44 isoforms expressed in cancer cells at the invasive tumour front was associated with patient prognosis. No conventional clinicopathological factors were independently associated with CD44 expression at the invasive tumour front. CONCLUSIONS: CD44-positive cancer stem-like cells at the invasive tumour front indicate poor survival and can be a unique biological prognostic factor for GC. Nature Publishing Group 2017-01-17 2016-12-08 /pmc/articles/PMC5243989/ /pubmed/27931044 http://dx.doi.org/10.1038/bjc.2016.401 Text en Copyright © 2017 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
Kodama, Hirokazu
Murata, Satoshi
Ishida, Mitsuaki
Yamamoto, Hiroshi
Yamaguchi, Tsuyoshi
Kaida, Sachiko
Miyake, Tohru
Takebayashi, Katsushi
Kushima, Ryoji
Tani, Masaji
Prognostic impact of CD44-positive cancer stem-like cells at the invasive front of gastric cancer
title Prognostic impact of CD44-positive cancer stem-like cells at the invasive front of gastric cancer
title_full Prognostic impact of CD44-positive cancer stem-like cells at the invasive front of gastric cancer
title_fullStr Prognostic impact of CD44-positive cancer stem-like cells at the invasive front of gastric cancer
title_full_unstemmed Prognostic impact of CD44-positive cancer stem-like cells at the invasive front of gastric cancer
title_short Prognostic impact of CD44-positive cancer stem-like cells at the invasive front of gastric cancer
title_sort prognostic impact of cd44-positive cancer stem-like cells at the invasive front of gastric cancer
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243989/
https://www.ncbi.nlm.nih.gov/pubmed/27931044
http://dx.doi.org/10.1038/bjc.2016.401
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