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TFF-1 Functions to Suppress Multiple Phenotypes Associated with Lung Cancer Progression
INTRODUCTION: Trefoil Factor (TFF) is a member of a protein family comprised of three isoforms, of which TFF-1 exhibits antithetical functions; promotion or suppression of cell proliferation, survival and invasion, depending on the cancer type. However, the pathobiological function of TFF-1 in lung...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439977/ https://www.ncbi.nlm.nih.gov/pubmed/34531663 http://dx.doi.org/10.2147/OTT.S322697 |
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author | Minegishi, Kentaro Dobashi, Yoh Tsubochi, Hiroyoshi Hagiwara, Koichi Ishibashi, Yuko Nomura, Sachiyo Nakamura, Ritsuko Ohmoto, Yasukazu Endo, Shunsuke |
author_facet | Minegishi, Kentaro Dobashi, Yoh Tsubochi, Hiroyoshi Hagiwara, Koichi Ishibashi, Yuko Nomura, Sachiyo Nakamura, Ritsuko Ohmoto, Yasukazu Endo, Shunsuke |
author_sort | Minegishi, Kentaro |
collection | PubMed |
description | INTRODUCTION: Trefoil Factor (TFF) is a member of a protein family comprised of three isoforms, of which TFF-1 exhibits antithetical functions; promotion or suppression of cell proliferation, survival and invasion, depending on the cancer type. However, the pathobiological function of TFF-1 in lung carcinoma has been still unclear. METHODS: We examined the expression and secretion of TFF-1 using cultured human lung carcinoma cells by immunoblotting, immunofluorescence, enzyme-linked immunosorbent assay and quantitative real-time PCR analyses. The effects of TFF-1 on various phenotypes were analyzed in two cell lines, including those transfected with cDNA encoding TFF-1. Cell proliferation and death were examined by hemocytometer cell counting and by colorimetric viability/cytotoxicity assay. Cell cycle profile, migration and invasion were also examined by flow cytometry, wound healing assay and Matrigel Transwell assay, respectively. The effect of TFF-1 overexpression was confirmed by additional transfection of TFF-1-specific siRNA. RESULTS: Endogenous TFF-1 protein expression and secretion into the media were observed exclusively in adenocarcinoma-derived cell lines. Forced overexpression of TFF-1 drove cell cycle transition, while the proliferation decreased by 19% to 25% due to increased cell death. This cell death was predominantly caused by apoptosis, as assessed by the activation of caspase 3/7. Cell migration was also suppressed by 71% to 82% in TFF-1-transfected cells. The suppressive effect of TFF-1 on proliferation and migration was restored by transfection of TFF-1 siRNA. Moreover, invasion was also suppressed to 77% to 83% in TFF-1-transfected cells. CONCLUSION: These findings reveal that TFF-1 functions as a suppressor of cancer proliferation by induction of apoptosis, cell migration and invasion and thus may provide a synergistic target for potential treatment strategies for human lung carcinoma. |
format | Online Article Text |
id | pubmed-8439977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-84399772021-09-15 TFF-1 Functions to Suppress Multiple Phenotypes Associated with Lung Cancer Progression Minegishi, Kentaro Dobashi, Yoh Tsubochi, Hiroyoshi Hagiwara, Koichi Ishibashi, Yuko Nomura, Sachiyo Nakamura, Ritsuko Ohmoto, Yasukazu Endo, Shunsuke Onco Targets Ther Original Research INTRODUCTION: Trefoil Factor (TFF) is a member of a protein family comprised of three isoforms, of which TFF-1 exhibits antithetical functions; promotion or suppression of cell proliferation, survival and invasion, depending on the cancer type. However, the pathobiological function of TFF-1 in lung carcinoma has been still unclear. METHODS: We examined the expression and secretion of TFF-1 using cultured human lung carcinoma cells by immunoblotting, immunofluorescence, enzyme-linked immunosorbent assay and quantitative real-time PCR analyses. The effects of TFF-1 on various phenotypes were analyzed in two cell lines, including those transfected with cDNA encoding TFF-1. Cell proliferation and death were examined by hemocytometer cell counting and by colorimetric viability/cytotoxicity assay. Cell cycle profile, migration and invasion were also examined by flow cytometry, wound healing assay and Matrigel Transwell assay, respectively. The effect of TFF-1 overexpression was confirmed by additional transfection of TFF-1-specific siRNA. RESULTS: Endogenous TFF-1 protein expression and secretion into the media were observed exclusively in adenocarcinoma-derived cell lines. Forced overexpression of TFF-1 drove cell cycle transition, while the proliferation decreased by 19% to 25% due to increased cell death. This cell death was predominantly caused by apoptosis, as assessed by the activation of caspase 3/7. Cell migration was also suppressed by 71% to 82% in TFF-1-transfected cells. The suppressive effect of TFF-1 on proliferation and migration was restored by transfection of TFF-1 siRNA. Moreover, invasion was also suppressed to 77% to 83% in TFF-1-transfected cells. CONCLUSION: These findings reveal that TFF-1 functions as a suppressor of cancer proliferation by induction of apoptosis, cell migration and invasion and thus may provide a synergistic target for potential treatment strategies for human lung carcinoma. Dove 2021-09-10 /pmc/articles/PMC8439977/ /pubmed/34531663 http://dx.doi.org/10.2147/OTT.S322697 Text en © 2021 Minegishi et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Minegishi, Kentaro Dobashi, Yoh Tsubochi, Hiroyoshi Hagiwara, Koichi Ishibashi, Yuko Nomura, Sachiyo Nakamura, Ritsuko Ohmoto, Yasukazu Endo, Shunsuke TFF-1 Functions to Suppress Multiple Phenotypes Associated with Lung Cancer Progression |
title | TFF-1 Functions to Suppress Multiple Phenotypes Associated with Lung Cancer Progression |
title_full | TFF-1 Functions to Suppress Multiple Phenotypes Associated with Lung Cancer Progression |
title_fullStr | TFF-1 Functions to Suppress Multiple Phenotypes Associated with Lung Cancer Progression |
title_full_unstemmed | TFF-1 Functions to Suppress Multiple Phenotypes Associated with Lung Cancer Progression |
title_short | TFF-1 Functions to Suppress Multiple Phenotypes Associated with Lung Cancer Progression |
title_sort | tff-1 functions to suppress multiple phenotypes associated with lung cancer progression |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439977/ https://www.ncbi.nlm.nih.gov/pubmed/34531663 http://dx.doi.org/10.2147/OTT.S322697 |
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