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Three-dimensional (3D) cell culture: a valuable step in advancing treatments for human hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is the fifth most common malignant cancer and the third most frequent cause of tumour-related mortality worldwide. Currently, several surgical and medical therapeutic strategies are available for HCCs; however, the interaction between neoplastic cells and non-neoplasti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339175/ https://www.ncbi.nlm.nih.gov/pubmed/35908054 http://dx.doi.org/10.1186/s12935-022-02662-3 |
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author | Khafaga, Asmaa F. Mousa, Shaker A. Aleya, Lotfi Abdel-Daim, Mohamed M. |
author_facet | Khafaga, Asmaa F. Mousa, Shaker A. Aleya, Lotfi Abdel-Daim, Mohamed M. |
author_sort | Khafaga, Asmaa F. |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is the fifth most common malignant cancer and the third most frequent cause of tumour-related mortality worldwide. Currently, several surgical and medical therapeutic strategies are available for HCCs; however, the interaction between neoplastic cells and non-neoplastic stromal cells within the tumour microenvironment (TME) results in strong therapeutic resistance of HCCs to conventional treatment. Therefore, the development of novel treatments is urgently needed to improve the survival of patients with HCC. The first step in developing efficient chemotherapeutic drugs is the establishment of an appropriate system for studying complex tumour culture and microenvironment interactions. Three-dimensional (3D) culture model might be a crucial bridge between in vivo and in vitro due to its ability to mimic the naturally complicated in vivo TME compared to conventional two-dimensional (2D) cultures. In this review, we shed light on various established 3D culture models of HCC and their role in the investigation of tumour-TME interactions and HCC-related therapeutic resistance. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-9339175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93391752022-08-01 Three-dimensional (3D) cell culture: a valuable step in advancing treatments for human hepatocellular carcinoma Khafaga, Asmaa F. Mousa, Shaker A. Aleya, Lotfi Abdel-Daim, Mohamed M. Cancer Cell Int Review Hepatocellular carcinoma (HCC) is the fifth most common malignant cancer and the third most frequent cause of tumour-related mortality worldwide. Currently, several surgical and medical therapeutic strategies are available for HCCs; however, the interaction between neoplastic cells and non-neoplastic stromal cells within the tumour microenvironment (TME) results in strong therapeutic resistance of HCCs to conventional treatment. Therefore, the development of novel treatments is urgently needed to improve the survival of patients with HCC. The first step in developing efficient chemotherapeutic drugs is the establishment of an appropriate system for studying complex tumour culture and microenvironment interactions. Three-dimensional (3D) culture model might be a crucial bridge between in vivo and in vitro due to its ability to mimic the naturally complicated in vivo TME compared to conventional two-dimensional (2D) cultures. In this review, we shed light on various established 3D culture models of HCC and their role in the investigation of tumour-TME interactions and HCC-related therapeutic resistance. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2022-07-30 /pmc/articles/PMC9339175/ /pubmed/35908054 http://dx.doi.org/10.1186/s12935-022-02662-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Khafaga, Asmaa F. Mousa, Shaker A. Aleya, Lotfi Abdel-Daim, Mohamed M. Three-dimensional (3D) cell culture: a valuable step in advancing treatments for human hepatocellular carcinoma |
title | Three-dimensional (3D) cell culture: a valuable step in advancing treatments for human hepatocellular carcinoma |
title_full | Three-dimensional (3D) cell culture: a valuable step in advancing treatments for human hepatocellular carcinoma |
title_fullStr | Three-dimensional (3D) cell culture: a valuable step in advancing treatments for human hepatocellular carcinoma |
title_full_unstemmed | Three-dimensional (3D) cell culture: a valuable step in advancing treatments for human hepatocellular carcinoma |
title_short | Three-dimensional (3D) cell culture: a valuable step in advancing treatments for human hepatocellular carcinoma |
title_sort | three-dimensional (3d) cell culture: a valuable step in advancing treatments for human hepatocellular carcinoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339175/ https://www.ncbi.nlm.nih.gov/pubmed/35908054 http://dx.doi.org/10.1186/s12935-022-02662-3 |
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