Unlocking the Potential Role of Decellularized Biological Scaffolds as a 3D Radiobiological Model for Low- and High-LET Irradiation
Decellularized extracellular matrix (ECM) bioscaffolds have emerged as a promising three-dimensional (3D) model, but so far there are no data concerning their use in radiobiological studies. We seeded two well-known radioresistant cell lines (HMV-II and PANC-1) in decellularized porcine liver-derive...
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Veröffentlicht in: | Cancers 2024-07, Vol.16 (14), p.2582 |
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creator | Charalampopoulou, Alexandra Barcellini, Amelia Peloso, Andrea Vanoli, Alessandro Cesari, Stefania Icaro Cornaglia, Antonia Bistika, Margarita Croce, Stefania Cobianchi, Lorenzo Ivaldi, Giovanni Battista Locati, Laura Deborah Magro, Giuseppe Tabarelli de Fatis, Paola Pullia, Marco Giuseppe Orlandi, Ester Facoetti, Angelica |
description | Decellularized extracellular matrix (ECM) bioscaffolds have emerged as a promising three-dimensional (3D) model, but so far there are no data concerning their use in radiobiological studies.
We seeded two well-known radioresistant cell lines (HMV-II and PANC-1) in decellularized porcine liver-derived scaffolds and irradiated them with both high- (Carbon Ions) and low- (Photons) Linear Energy Transfer (LET) radiation in order to test whether a natural 3D-bioscaffold might be a useful tool for radiobiological research and to achieve an evaluation that could be as near as possible to what happens in vivo.
Biological scaffolds provided a favorable 3D environment for cell proliferation and expansion. Cells did not show signs of dedifferentiation and retained their distinct phenotype coherently with their anatomopathological and clinical behaviors. The radiobiological response to high LET was higher for HMV-II and PANC-1 compared to the low LET. In particular, Carbon Ions reduced the melanogenesis in HMV-II and induced more cytopathic effects and the substantial cell deterioration of both cell lines compared to photons.
In addition to offering a suitable 3D model for radiobiological research and an appropriate setting for preclinical oncological analysis, we can attest that bioscaffolds seemed cost-effective due to their ease of use, low maintenance requirements, and lack of complex technology. |
doi_str_mv | 10.3390/cancers16142582 |
format | Article |
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We seeded two well-known radioresistant cell lines (HMV-II and PANC-1) in decellularized porcine liver-derived scaffolds and irradiated them with both high- (Carbon Ions) and low- (Photons) Linear Energy Transfer (LET) radiation in order to test whether a natural 3D-bioscaffold might be a useful tool for radiobiological research and to achieve an evaluation that could be as near as possible to what happens in vivo.
Biological scaffolds provided a favorable 3D environment for cell proliferation and expansion. Cells did not show signs of dedifferentiation and retained their distinct phenotype coherently with their anatomopathological and clinical behaviors. The radiobiological response to high LET was higher for HMV-II and PANC-1 compared to the low LET. In particular, Carbon Ions reduced the melanogenesis in HMV-II and induced more cytopathic effects and the substantial cell deterioration of both cell lines compared to photons.
In addition to offering a suitable 3D model for radiobiological research and an appropriate setting for preclinical oncological analysis, we can attest that bioscaffolds seemed cost-effective due to their ease of use, low maintenance requirements, and lack of complex technology.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers16142582</identifier><identifier>PMID: 39061220</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Carbon ; Cell proliferation ; Collagen ; Extracellular matrix ; Hepatocytes ; Histology ; Ions ; Liver ; Melanoma ; Morphology ; Penicillin ; Phenotypes ; Photons ; Radiation ; Radiation therapy ; Skin cancer ; Tumor microenvironment</subject><ispartof>Cancers, 2024-07, Vol.16 (14), p.2582</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c317t-3fa0d8675f07877a77beafa345cbba6fcbaf9c631858790fb3e12a02854b5e533</cites><orcidid>0000-0001-9152-590X ; 0000-0002-2976-7032 ; 0000-0002-7280-5698 ; 0000-0002-6773-5453 ; 0000-0003-3315-2580 ; 0000-0002-8690-9420 ; 0000-0001-8215-9258 ; 0000-0001-7140-8642 ; 0000-0002-1595-104X ; 0000-0001-6495-8574 ; 0000-0003-1851-431X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39061220$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Charalampopoulou, Alexandra</creatorcontrib><creatorcontrib>Barcellini, Amelia</creatorcontrib><creatorcontrib>Peloso, Andrea</creatorcontrib><creatorcontrib>Vanoli, Alessandro</creatorcontrib><creatorcontrib>Cesari, Stefania</creatorcontrib><creatorcontrib>Icaro Cornaglia, Antonia</creatorcontrib><creatorcontrib>Bistika, Margarita</creatorcontrib><creatorcontrib>Croce, Stefania</creatorcontrib><creatorcontrib>Cobianchi, Lorenzo</creatorcontrib><creatorcontrib>Ivaldi, Giovanni Battista</creatorcontrib><creatorcontrib>Locati, Laura Deborah</creatorcontrib><creatorcontrib>Magro, Giuseppe</creatorcontrib><creatorcontrib>Tabarelli de Fatis, Paola</creatorcontrib><creatorcontrib>Pullia, Marco Giuseppe</creatorcontrib><creatorcontrib>Orlandi, Ester</creatorcontrib><creatorcontrib>Facoetti, Angelica</creatorcontrib><title>Unlocking the Potential Role of Decellularized Biological Scaffolds as a 3D Radiobiological Model for Low- and High-LET Irradiation</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>Decellularized extracellular matrix (ECM) bioscaffolds have emerged as a promising three-dimensional (3D) model, but so far there are no data concerning their use in radiobiological studies.
We seeded two well-known radioresistant cell lines (HMV-II and PANC-1) in decellularized porcine liver-derived scaffolds and irradiated them with both high- (Carbon Ions) and low- (Photons) Linear Energy Transfer (LET) radiation in order to test whether a natural 3D-bioscaffold might be a useful tool for radiobiological research and to achieve an evaluation that could be as near as possible to what happens in vivo.
Biological scaffolds provided a favorable 3D environment for cell proliferation and expansion. Cells did not show signs of dedifferentiation and retained their distinct phenotype coherently with their anatomopathological and clinical behaviors. The radiobiological response to high LET was higher for HMV-II and PANC-1 compared to the low LET. In particular, Carbon Ions reduced the melanogenesis in HMV-II and induced more cytopathic effects and the substantial cell deterioration of both cell lines compared to photons.
In addition to offering a suitable 3D model for radiobiological research and an appropriate setting for preclinical oncological analysis, we can attest that bioscaffolds seemed cost-effective due to their ease of use, low maintenance requirements, and lack of complex technology.</description><subject>Carbon</subject><subject>Cell proliferation</subject><subject>Collagen</subject><subject>Extracellular matrix</subject><subject>Hepatocytes</subject><subject>Histology</subject><subject>Ions</subject><subject>Liver</subject><subject>Melanoma</subject><subject>Morphology</subject><subject>Penicillin</subject><subject>Phenotypes</subject><subject>Photons</subject><subject>Radiation</subject><subject>Radiation therapy</subject><subject>Skin cancer</subject><subject>Tumor microenvironment</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkc1rFTEUxQdRbKldu5OAGzfT5mPyMcvaVlt4otR2PdzJ3Lym5iU1mUF06z9uHq1ai7mBewm_cznhNM1LRg-E6OmhhWgxF6ZYx6XhT5pdTjVvleq7pw_mnWa_lBtajxBMK_282alqxTinu83PqxiS_eLjmszXSD6lGePsIZCLFJAkR07QYghLgOx_4ETe-hTS2ttKfLbgXApTIVAvESfkAiafxr_EhzRhIC5lskrfWgJxImd-fd2uTi_Jec6Vhtmn-KJ55iAU3L_ve83Vu9PL47N29fH9-fHRqrXV99wKB3QySktHtdEatB4RHIhO2nEE5ewIrrdKMCON7qkbBTIOlBvZjRKlEHvNm7u9tzl9XbDMw8aX7e8gYlrKIKiRjHWylxV9_Qi9SUuO1d2W6jQ3ij6g1hBw8NGlOYPdLh2ODBVadZT1lTr4D1Vrwo23KaLz9f0fweGdwOZUSkY33Ga_gfx9YHTYJj88Sr4qXt3bXcYNTn_43zmLX_UnqF4</recordid><startdate>20240718</startdate><enddate>20240718</enddate><creator>Charalampopoulou, Alexandra</creator><creator>Barcellini, Amelia</creator><creator>Peloso, Andrea</creator><creator>Vanoli, Alessandro</creator><creator>Cesari, Stefania</creator><creator>Icaro Cornaglia, Antonia</creator><creator>Bistika, Margarita</creator><creator>Croce, Stefania</creator><creator>Cobianchi, Lorenzo</creator><creator>Ivaldi, Giovanni Battista</creator><creator>Locati, Laura Deborah</creator><creator>Magro, Giuseppe</creator><creator>Tabarelli de Fatis, Paola</creator><creator>Pullia, Marco Giuseppe</creator><creator>Orlandi, Ester</creator><creator>Facoetti, Angelica</creator><general>MDPI AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9152-590X</orcidid><orcidid>https://orcid.org/0000-0002-2976-7032</orcidid><orcidid>https://orcid.org/0000-0002-7280-5698</orcidid><orcidid>https://orcid.org/0000-0002-6773-5453</orcidid><orcidid>https://orcid.org/0000-0003-3315-2580</orcidid><orcidid>https://orcid.org/0000-0002-8690-9420</orcidid><orcidid>https://orcid.org/0000-0001-8215-9258</orcidid><orcidid>https://orcid.org/0000-0001-7140-8642</orcidid><orcidid>https://orcid.org/0000-0002-1595-104X</orcidid><orcidid>https://orcid.org/0000-0001-6495-8574</orcidid><orcidid>https://orcid.org/0000-0003-1851-431X</orcidid></search><sort><creationdate>20240718</creationdate><title>Unlocking the Potential Role of Decellularized Biological Scaffolds as a 3D Radiobiological Model for Low- and High-LET Irradiation</title><author>Charalampopoulou, Alexandra ; Barcellini, Amelia ; Peloso, Andrea ; Vanoli, Alessandro ; Cesari, Stefania ; Icaro Cornaglia, Antonia ; Bistika, Margarita ; Croce, Stefania ; Cobianchi, Lorenzo ; Ivaldi, Giovanni Battista ; Locati, Laura Deborah ; Magro, Giuseppe ; Tabarelli de Fatis, Paola ; Pullia, Marco Giuseppe ; Orlandi, Ester ; Facoetti, Angelica</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c317t-3fa0d8675f07877a77beafa345cbba6fcbaf9c631858790fb3e12a02854b5e533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Carbon</topic><topic>Cell proliferation</topic><topic>Collagen</topic><topic>Extracellular matrix</topic><topic>Hepatocytes</topic><topic>Histology</topic><topic>Ions</topic><topic>Liver</topic><topic>Melanoma</topic><topic>Morphology</topic><topic>Penicillin</topic><topic>Phenotypes</topic><topic>Photons</topic><topic>Radiation</topic><topic>Radiation therapy</topic><topic>Skin cancer</topic><topic>Tumor microenvironment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Charalampopoulou, Alexandra</creatorcontrib><creatorcontrib>Barcellini, Amelia</creatorcontrib><creatorcontrib>Peloso, Andrea</creatorcontrib><creatorcontrib>Vanoli, Alessandro</creatorcontrib><creatorcontrib>Cesari, Stefania</creatorcontrib><creatorcontrib>Icaro Cornaglia, Antonia</creatorcontrib><creatorcontrib>Bistika, Margarita</creatorcontrib><creatorcontrib>Croce, Stefania</creatorcontrib><creatorcontrib>Cobianchi, Lorenzo</creatorcontrib><creatorcontrib>Ivaldi, Giovanni Battista</creatorcontrib><creatorcontrib>Locati, Laura Deborah</creatorcontrib><creatorcontrib>Magro, Giuseppe</creatorcontrib><creatorcontrib>Tabarelli de Fatis, Paola</creatorcontrib><creatorcontrib>Pullia, Marco Giuseppe</creatorcontrib><creatorcontrib>Orlandi, Ester</creatorcontrib><creatorcontrib>Facoetti, Angelica</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Charalampopoulou, Alexandra</au><au>Barcellini, Amelia</au><au>Peloso, Andrea</au><au>Vanoli, Alessandro</au><au>Cesari, Stefania</au><au>Icaro Cornaglia, Antonia</au><au>Bistika, Margarita</au><au>Croce, Stefania</au><au>Cobianchi, Lorenzo</au><au>Ivaldi, Giovanni Battista</au><au>Locati, Laura Deborah</au><au>Magro, Giuseppe</au><au>Tabarelli de Fatis, Paola</au><au>Pullia, Marco Giuseppe</au><au>Orlandi, Ester</au><au>Facoetti, Angelica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unlocking the Potential Role of Decellularized Biological Scaffolds as a 3D Radiobiological Model for Low- and High-LET Irradiation</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2024-07-18</date><risdate>2024</risdate><volume>16</volume><issue>14</issue><spage>2582</spage><pages>2582-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Decellularized extracellular matrix (ECM) bioscaffolds have emerged as a promising three-dimensional (3D) model, but so far there are no data concerning their use in radiobiological studies.
We seeded two well-known radioresistant cell lines (HMV-II and PANC-1) in decellularized porcine liver-derived scaffolds and irradiated them with both high- (Carbon Ions) and low- (Photons) Linear Energy Transfer (LET) radiation in order to test whether a natural 3D-bioscaffold might be a useful tool for radiobiological research and to achieve an evaluation that could be as near as possible to what happens in vivo.
Biological scaffolds provided a favorable 3D environment for cell proliferation and expansion. Cells did not show signs of dedifferentiation and retained their distinct phenotype coherently with their anatomopathological and clinical behaviors. The radiobiological response to high LET was higher for HMV-II and PANC-1 compared to the low LET. In particular, Carbon Ions reduced the melanogenesis in HMV-II and induced more cytopathic effects and the substantial cell deterioration of both cell lines compared to photons.
In addition to offering a suitable 3D model for radiobiological research and an appropriate setting for preclinical oncological analysis, we can attest that bioscaffolds seemed cost-effective due to their ease of use, low maintenance requirements, and lack of complex technology.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39061220</pmid><doi>10.3390/cancers16142582</doi><orcidid>https://orcid.org/0000-0001-9152-590X</orcidid><orcidid>https://orcid.org/0000-0002-2976-7032</orcidid><orcidid>https://orcid.org/0000-0002-7280-5698</orcidid><orcidid>https://orcid.org/0000-0002-6773-5453</orcidid><orcidid>https://orcid.org/0000-0003-3315-2580</orcidid><orcidid>https://orcid.org/0000-0002-8690-9420</orcidid><orcidid>https://orcid.org/0000-0001-8215-9258</orcidid><orcidid>https://orcid.org/0000-0001-7140-8642</orcidid><orcidid>https://orcid.org/0000-0002-1595-104X</orcidid><orcidid>https://orcid.org/0000-0001-6495-8574</orcidid><orcidid>https://orcid.org/0000-0003-1851-431X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Carbon Cell proliferation Collagen Extracellular matrix Hepatocytes Histology Ions Liver Melanoma Morphology Penicillin Phenotypes Photons Radiation Radiation therapy Skin cancer Tumor microenvironment |
title | Unlocking the Potential Role of Decellularized Biological Scaffolds as a 3D Radiobiological Model for Low- and High-LET Irradiation |
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