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Association of surfactant protein D with pulmonary metastases from colon cancer

Surfactant protein D (SP-D) is a member of the collectin family of proteins, which is secreted by airway epithelial cells. SP-D serves an important role in the immune system and in the inflammatory regulation of the lung. SP-D was recently found to suppress lung cancer progression by downregulating...

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Autores principales: Tajima, Yuki, Tsuruta, Masashi, Hasegawa, Hirotoshi, Okabayashi, Koji, Ishida, Takashi, Yahagi, Masashi, Makino, Akitsugu, Koishikawa, Kaoru, Akimoto, Shingo, Sin, Don D., Kitagawa, Yuko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583848/
https://www.ncbi.nlm.nih.gov/pubmed/33123238
http://dx.doi.org/10.3892/ol.2020.12185
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author Tajima, Yuki
Tsuruta, Masashi
Hasegawa, Hirotoshi
Okabayashi, Koji
Ishida, Takashi
Yahagi, Masashi
Makino, Akitsugu
Koishikawa, Kaoru
Akimoto, Shingo
Sin, Don D.
Kitagawa, Yuko
author_facet Tajima, Yuki
Tsuruta, Masashi
Hasegawa, Hirotoshi
Okabayashi, Koji
Ishida, Takashi
Yahagi, Masashi
Makino, Akitsugu
Koishikawa, Kaoru
Akimoto, Shingo
Sin, Don D.
Kitagawa, Yuko
author_sort Tajima, Yuki
collection PubMed
description Surfactant protein D (SP-D) is a member of the collectin family of proteins, which is secreted by airway epithelial cells. SP-D serves an important role in the immune system and in the inflammatory regulation of the lung. SP-D was recently found to suppress lung cancer progression by downregulating epidermal growth factor signaling. However, the relationship between SP-D and pulmonary metastases from colon cancer remains unknown. The present study aimed to determine whether SP-D may suppress the development of the mouse rectal carcinoma cell line, CMT93, in vitro. The present study investigated the effect of SP-D on pulmonary metastases from colon cancer in vivo using SP-D knockout mice. A wound healing assay and cell invasion assay revealed that SP-D suppressed the proliferation, migration and invasion of CMT-93 cells. After injection of CMT-93 cells into the tail vein, SP-D knockout mice were significantly more susceptible to developing pulmonary metastases than C57/BL6 mice (control). Moreover, a novel cell line (CMT-93 pulmonary metastasis; CMT-93 PM) was established from the lesions of pulmonary metastases in C57/BL6 mice following injection of CMT93 into the tail vein. CMT-93 PM exhibited more robust invasion and proliferation compared to CMT93, which was unaffected by exposure to SP-D. A higher incidence of pulmonary metastases was detected following injection of CMT93 PM into the tail vein of C57/BL6 mice compared with CMT-93. Consequently, SP-D may be involved in the pathogenesis of pulmonary metastases from colon cancer.
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spelling pubmed-75838482020-10-28 Association of surfactant protein D with pulmonary metastases from colon cancer Tajima, Yuki Tsuruta, Masashi Hasegawa, Hirotoshi Okabayashi, Koji Ishida, Takashi Yahagi, Masashi Makino, Akitsugu Koishikawa, Kaoru Akimoto, Shingo Sin, Don D. Kitagawa, Yuko Oncol Lett Articles Surfactant protein D (SP-D) is a member of the collectin family of proteins, which is secreted by airway epithelial cells. SP-D serves an important role in the immune system and in the inflammatory regulation of the lung. SP-D was recently found to suppress lung cancer progression by downregulating epidermal growth factor signaling. However, the relationship between SP-D and pulmonary metastases from colon cancer remains unknown. The present study aimed to determine whether SP-D may suppress the development of the mouse rectal carcinoma cell line, CMT93, in vitro. The present study investigated the effect of SP-D on pulmonary metastases from colon cancer in vivo using SP-D knockout mice. A wound healing assay and cell invasion assay revealed that SP-D suppressed the proliferation, migration and invasion of CMT-93 cells. After injection of CMT-93 cells into the tail vein, SP-D knockout mice were significantly more susceptible to developing pulmonary metastases than C57/BL6 mice (control). Moreover, a novel cell line (CMT-93 pulmonary metastasis; CMT-93 PM) was established from the lesions of pulmonary metastases in C57/BL6 mice following injection of CMT93 into the tail vein. CMT-93 PM exhibited more robust invasion and proliferation compared to CMT93, which was unaffected by exposure to SP-D. A higher incidence of pulmonary metastases was detected following injection of CMT93 PM into the tail vein of C57/BL6 mice compared with CMT-93. Consequently, SP-D may be involved in the pathogenesis of pulmonary metastases from colon cancer. D.A. Spandidos 2020-12 2020-10-05 /pmc/articles/PMC7583848/ /pubmed/33123238 http://dx.doi.org/10.3892/ol.2020.12185 Text en Copyright: © Tajima et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Tajima, Yuki
Tsuruta, Masashi
Hasegawa, Hirotoshi
Okabayashi, Koji
Ishida, Takashi
Yahagi, Masashi
Makino, Akitsugu
Koishikawa, Kaoru
Akimoto, Shingo
Sin, Don D.
Kitagawa, Yuko
Association of surfactant protein D with pulmonary metastases from colon cancer
title Association of surfactant protein D with pulmonary metastases from colon cancer
title_full Association of surfactant protein D with pulmonary metastases from colon cancer
title_fullStr Association of surfactant protein D with pulmonary metastases from colon cancer
title_full_unstemmed Association of surfactant protein D with pulmonary metastases from colon cancer
title_short Association of surfactant protein D with pulmonary metastases from colon cancer
title_sort association of surfactant protein d with pulmonary metastases from colon cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583848/
https://www.ncbi.nlm.nih.gov/pubmed/33123238
http://dx.doi.org/10.3892/ol.2020.12185
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