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Human lung cancer cells grown in an ex vivo 3D lung model produce matrix metalloproteinases not produced in 2D culture
We compared the growth of human lung cancer cells in an ex vivo three-dimensional (3D) lung model and 2D culture to determine which better mimics lung cancer growth in patients. A549 cells were grown in an ex vivo 3D lung model and in 2D culture for 15 days. We measured the size and formation of tum...
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Published in: | PloS one 2012-09, Vol.7 (9), p.e45308-e45308 |
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description | We compared the growth of human lung cancer cells in an ex vivo three-dimensional (3D) lung model and 2D culture to determine which better mimics lung cancer growth in patients. A549 cells were grown in an ex vivo 3D lung model and in 2D culture for 15 days. We measured the size and formation of tumor nodules and counted the cells after 15 days. We also stained the tissue/cells for Ki-67, and Caspase-3. We measured matrix metalloproteinase (MMP) levels in the conditioned media and in blood plasma from patients with adenocarcinoma of the lung. Organized tumor nodules with intact vascular space formed in the ex vivo 3D lung model but not in 2D culture. Proliferation and apoptosis were greater in the ex vivo 3D lung model compared to the 2D culture. After 15 days, there were significantly more cells in the 2D culture than the 3D model. MMP-1, MMP-9, and MMP-10 production were significantly greater in the ex vivo 3D lung model. There was no production of MMP-9 in the 2D culture. The patient samples contained MMP-1, MMP-2, MMP-9, and MMP-10. The human lung cancer cells grown on ex vivo 3D model form perfusable nodules that grow over time. It also produced MMPs that were not produced in 2D culture but seen in human lung cancer patients. The ex vivo 3D lung model may more closely mimic the biology of human lung cancer development than the 2D culture. |
doi_str_mv | 10.1371/journal.pone.0045308 |
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A549 cells were grown in an ex vivo 3D lung model and in 2D culture for 15 days. We measured the size and formation of tumor nodules and counted the cells after 15 days. We also stained the tissue/cells for Ki-67, and Caspase-3. We measured matrix metalloproteinase (MMP) levels in the conditioned media and in blood plasma from patients with adenocarcinoma of the lung. Organized tumor nodules with intact vascular space formed in the ex vivo 3D lung model but not in 2D culture. Proliferation and apoptosis were greater in the ex vivo 3D lung model compared to the 2D culture. After 15 days, there were significantly more cells in the 2D culture than the 3D model. MMP-1, MMP-9, and MMP-10 production were significantly greater in the ex vivo 3D lung model. There was no production of MMP-9 in the 2D culture. The patient samples contained MMP-1, MMP-2, MMP-9, and MMP-10. The human lung cancer cells grown on ex vivo 3D model form perfusable nodules that grow over time. It also produced MMPs that were not produced in 2D culture but seen in human lung cancer patients. The ex vivo 3D lung model may more closely mimic the biology of human lung cancer development than the 2D culture.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0045308</identifier><identifier>PMID: 23028922</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adenocarcinoma ; Analysis ; Apoptosis ; Biology ; Blood plasma ; Cancer ; Cancer cells ; Cancer therapies ; Caspase ; Caspase-3 ; Cell culture ; Cell Culture Techniques - methods ; Cell death ; Cell Line, Tumor ; Conditioning ; Extracellular matrix ; Gelatinase A ; Gelatinase B ; Gene expression ; Genetic aspects ; Growth ; Humans ; Interstitial collagenase ; Lung cancer ; Lung diseases ; Lung nodules ; Matrix metalloproteinase ; Matrix metalloproteinases ; Matrix Metalloproteinases - metabolism ; Media (culture) ; Medicine ; Metalloenzymes ; Metalloproteinase ; Methods ; Morphogenesis ; Nodules ; Patients ; Physiological aspects ; Reverse Transcriptase Polymerase Chain Reaction ; Rodents ; Stromelysin 2 ; Surgery ; Three dimensional models ; Trends ; Tumors ; Two dimensional models</subject><ispartof>PloS one, 2012-09, Vol.7 (9), p.e45308-e45308</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>Mishra et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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A549 cells were grown in an ex vivo 3D lung model and in 2D culture for 15 days. We measured the size and formation of tumor nodules and counted the cells after 15 days. We also stained the tissue/cells for Ki-67, and Caspase-3. We measured matrix metalloproteinase (MMP) levels in the conditioned media and in blood plasma from patients with adenocarcinoma of the lung. Organized tumor nodules with intact vascular space formed in the ex vivo 3D lung model but not in 2D culture. Proliferation and apoptosis were greater in the ex vivo 3D lung model compared to the 2D culture. After 15 days, there were significantly more cells in the 2D culture than the 3D model. MMP-1, MMP-9, and MMP-10 production were significantly greater in the ex vivo 3D lung model. There was no production of MMP-9 in the 2D culture. The patient samples contained MMP-1, MMP-2, MMP-9, and MMP-10. The human lung cancer cells grown on ex vivo 3D model form perfusable nodules that grow over time. 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The ex vivo 3D lung model may more closely mimic the biology of human lung cancer development than the 2D culture.</description><subject>Adenocarcinoma</subject><subject>Analysis</subject><subject>Apoptosis</subject><subject>Biology</subject><subject>Blood plasma</subject><subject>Cancer</subject><subject>Cancer cells</subject><subject>Cancer therapies</subject><subject>Caspase</subject><subject>Caspase-3</subject><subject>Cell culture</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell death</subject><subject>Cell Line, Tumor</subject><subject>Conditioning</subject><subject>Extracellular matrix</subject><subject>Gelatinase A</subject><subject>Gelatinase B</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Growth</subject><subject>Humans</subject><subject>Interstitial collagenase</subject><subject>Lung cancer</subject><subject>Lung diseases</subject><subject>Lung nodules</subject><subject>Matrix metalloproteinase</subject><subject>Matrix metalloproteinases</subject><subject>Matrix Metalloproteinases - 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A549 cells were grown in an ex vivo 3D lung model and in 2D culture for 15 days. We measured the size and formation of tumor nodules and counted the cells after 15 days. We also stained the tissue/cells for Ki-67, and Caspase-3. We measured matrix metalloproteinase (MMP) levels in the conditioned media and in blood plasma from patients with adenocarcinoma of the lung. Organized tumor nodules with intact vascular space formed in the ex vivo 3D lung model but not in 2D culture. Proliferation and apoptosis were greater in the ex vivo 3D lung model compared to the 2D culture. After 15 days, there were significantly more cells in the 2D culture than the 3D model. MMP-1, MMP-9, and MMP-10 production were significantly greater in the ex vivo 3D lung model. There was no production of MMP-9 in the 2D culture. The patient samples contained MMP-1, MMP-2, MMP-9, and MMP-10. The human lung cancer cells grown on ex vivo 3D model form perfusable nodules that grow over time. It also produced MMPs that were not produced in 2D culture but seen in human lung cancer patients. The ex vivo 3D lung model may more closely mimic the biology of human lung cancer development than the 2D culture.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23028922</pmid><doi>10.1371/journal.pone.0045308</doi><tpages>e45308</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Analysis Apoptosis Biology Blood plasma Cancer Cancer cells Cancer therapies Caspase Caspase-3 Cell culture Cell Culture Techniques - methods Cell death Cell Line, Tumor Conditioning Extracellular matrix Gelatinase A Gelatinase B Gene expression Genetic aspects Growth Humans Interstitial collagenase Lung cancer Lung diseases Lung nodules Matrix metalloproteinase Matrix metalloproteinases Matrix Metalloproteinases - metabolism Media (culture) Medicine Metalloenzymes Metalloproteinase Methods Morphogenesis Nodules Patients Physiological aspects Reverse Transcriptase Polymerase Chain Reaction Rodents Stromelysin 2 Surgery Three dimensional models Trends Tumors Two dimensional models |
title | Human lung cancer cells grown in an ex vivo 3D lung model produce matrix metalloproteinases not produced in 2D culture |
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