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Evaluation of the expression of bone marrow‐derived mesenchymal stem cells and cancer‐associated fibroblasts in the stroma of gastric cancer tissue

AIM: Cancer‐associated fibroblasts (CAFs) generated by bone marrow‐derived mesenchymal stem cells (BM‐MSCs) play an important role in cancer progression. In this study, we investigated the relationships of BM‐MSCs and CAFs in resected gastric cancers with the clinicopathological factors of patients....

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Autores principales: Minami, Taizan, Aoyagi, Keishiro, Kawahara, Akihiko, Murakami, Naotaka, Isobe, Taro, Tanaka, Yuya, Kaku, Hideaki, Fujita, Fumihiko, Akagi, Yoshito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382433/
https://www.ncbi.nlm.nih.gov/pubmed/32724891
http://dx.doi.org/10.1002/ags3.12347
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author Minami, Taizan
Aoyagi, Keishiro
Kawahara, Akihiko
Murakami, Naotaka
Isobe, Taro
Tanaka, Yuya
Kaku, Hideaki
Fujita, Fumihiko
Akagi, Yoshito
author_facet Minami, Taizan
Aoyagi, Keishiro
Kawahara, Akihiko
Murakami, Naotaka
Isobe, Taro
Tanaka, Yuya
Kaku, Hideaki
Fujita, Fumihiko
Akagi, Yoshito
author_sort Minami, Taizan
collection PubMed
description AIM: Cancer‐associated fibroblasts (CAFs) generated by bone marrow‐derived mesenchymal stem cells (BM‐MSCs) play an important role in cancer progression. In this study, we investigated the relationships of BM‐MSCs and CAFs in resected gastric cancers with the clinicopathological factors of patients. METHODS: We analyzed 120 gastric cancer patients who underwent gastrectomy. Immunostaining was performed with an anti‐CD271 antibody (BM‐MSCs) and anti‐α‐smooth muscle actin (αSMA) antibody (CAFs). Staining intensity was used to divide patients into low and high expression groups. Observation sites in cancer tissues were invasive, central, and whole portions. RESULTS: Expression of αSMA was significantly related to depth of tumor invasion (T), lymph node metastasis (N), lymphatic invasion (ly), venous invasion (v), and stage. Expression of CD271 was significantly related to v, stage, stromal volume, and tumor infiltration pattern (INF). Overall survival (OS) of the high expression group was significantly lower than that of the low expression group for both αSMA and CD271. Multivariate analysis showed that N, αSMA (whole), and CD271 (invasive) were independent prognostic factors. CONCLUSIONS: Cancer‐associated fibroblasts and BM‐MSCs are related to the progression, invasion, and prognosis of gastric cancer and may be therapeutic targets of gastric cancer.
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spelling pubmed-73824332020-07-27 Evaluation of the expression of bone marrow‐derived mesenchymal stem cells and cancer‐associated fibroblasts in the stroma of gastric cancer tissue Minami, Taizan Aoyagi, Keishiro Kawahara, Akihiko Murakami, Naotaka Isobe, Taro Tanaka, Yuya Kaku, Hideaki Fujita, Fumihiko Akagi, Yoshito Ann Gastroenterol Surg Original Articles AIM: Cancer‐associated fibroblasts (CAFs) generated by bone marrow‐derived mesenchymal stem cells (BM‐MSCs) play an important role in cancer progression. In this study, we investigated the relationships of BM‐MSCs and CAFs in resected gastric cancers with the clinicopathological factors of patients. METHODS: We analyzed 120 gastric cancer patients who underwent gastrectomy. Immunostaining was performed with an anti‐CD271 antibody (BM‐MSCs) and anti‐α‐smooth muscle actin (αSMA) antibody (CAFs). Staining intensity was used to divide patients into low and high expression groups. Observation sites in cancer tissues were invasive, central, and whole portions. RESULTS: Expression of αSMA was significantly related to depth of tumor invasion (T), lymph node metastasis (N), lymphatic invasion (ly), venous invasion (v), and stage. Expression of CD271 was significantly related to v, stage, stromal volume, and tumor infiltration pattern (INF). Overall survival (OS) of the high expression group was significantly lower than that of the low expression group for both αSMA and CD271. Multivariate analysis showed that N, αSMA (whole), and CD271 (invasive) were independent prognostic factors. CONCLUSIONS: Cancer‐associated fibroblasts and BM‐MSCs are related to the progression, invasion, and prognosis of gastric cancer and may be therapeutic targets of gastric cancer. John Wiley and Sons Inc. 2020-05-27 /pmc/articles/PMC7382433/ /pubmed/32724891 http://dx.doi.org/10.1002/ags3.12347 Text en © 2020 The Authors. Annals of Gastroenterological Surgery published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Gastroenterology Surgery This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Minami, Taizan
Aoyagi, Keishiro
Kawahara, Akihiko
Murakami, Naotaka
Isobe, Taro
Tanaka, Yuya
Kaku, Hideaki
Fujita, Fumihiko
Akagi, Yoshito
Evaluation of the expression of bone marrow‐derived mesenchymal stem cells and cancer‐associated fibroblasts in the stroma of gastric cancer tissue
title Evaluation of the expression of bone marrow‐derived mesenchymal stem cells and cancer‐associated fibroblasts in the stroma of gastric cancer tissue
title_full Evaluation of the expression of bone marrow‐derived mesenchymal stem cells and cancer‐associated fibroblasts in the stroma of gastric cancer tissue
title_fullStr Evaluation of the expression of bone marrow‐derived mesenchymal stem cells and cancer‐associated fibroblasts in the stroma of gastric cancer tissue
title_full_unstemmed Evaluation of the expression of bone marrow‐derived mesenchymal stem cells and cancer‐associated fibroblasts in the stroma of gastric cancer tissue
title_short Evaluation of the expression of bone marrow‐derived mesenchymal stem cells and cancer‐associated fibroblasts in the stroma of gastric cancer tissue
title_sort evaluation of the expression of bone marrow‐derived mesenchymal stem cells and cancer‐associated fibroblasts in the stroma of gastric cancer tissue
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382433/
https://www.ncbi.nlm.nih.gov/pubmed/32724891
http://dx.doi.org/10.1002/ags3.12347
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