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Advances in culture methods for acute myeloid leukemia research

Conventional suspension cultures have been used in Acute Myeloid Leukemia (AML) research to study its biology as well as to screen any drug molecules, since its inception. Co-culture models of AML cells and other stromal cells as well as 3 dimensional (3D) culture models have gained much attention r...

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Detalles Bibliográficos
Autores principales: Syama, Krishnapriya, Hassan, Eman M., Zou, Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336936/
https://www.ncbi.nlm.nih.gov/pubmed/34368398
http://dx.doi.org/10.18632/oncoscience.540
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author Syama, Krishnapriya
Hassan, Eman M.
Zou, Shan
author_facet Syama, Krishnapriya
Hassan, Eman M.
Zou, Shan
author_sort Syama, Krishnapriya
collection PubMed
description Conventional suspension cultures have been used in Acute Myeloid Leukemia (AML) research to study its biology as well as to screen any drug molecules, since its inception. Co-culture models of AML cells and other stromal cells as well as 3 dimensional (3D) culture models have gained much attention recently. These culture models try to recapitulate the tumour microenvironment and are found to be more suitable than suspension cultures. Though animal models are being used, they require more time, effort and facilities and hence, it is essential to develop cell culture models for high-throughput screening of drugs. Here, we discuss a new co-culture model developed by our research group involving acute myeloid leukemia (AML) cells and stimulated macrophages. Other studies on co-culture systems and relevance of 3D culture in leukemic research in understanding the pathology and treatment of leukemia are also reviewed.
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spelling pubmed-83369362021-08-05 Advances in culture methods for acute myeloid leukemia research Syama, Krishnapriya Hassan, Eman M. Zou, Shan Oncoscience Research Perspective Conventional suspension cultures have been used in Acute Myeloid Leukemia (AML) research to study its biology as well as to screen any drug molecules, since its inception. Co-culture models of AML cells and other stromal cells as well as 3 dimensional (3D) culture models have gained much attention recently. These culture models try to recapitulate the tumour microenvironment and are found to be more suitable than suspension cultures. Though animal models are being used, they require more time, effort and facilities and hence, it is essential to develop cell culture models for high-throughput screening of drugs. Here, we discuss a new co-culture model developed by our research group involving acute myeloid leukemia (AML) cells and stimulated macrophages. Other studies on co-culture systems and relevance of 3D culture in leukemic research in understanding the pathology and treatment of leukemia are also reviewed. Impact Journals LLC 2021-08-04 /pmc/articles/PMC8336936/ /pubmed/34368398 http://dx.doi.org/10.18632/oncoscience.540 Text en https://creativecommons.org/licenses/by/3.0/Copyright: © 2021 Syama et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Perspective
Syama, Krishnapriya
Hassan, Eman M.
Zou, Shan
Advances in culture methods for acute myeloid leukemia research
title Advances in culture methods for acute myeloid leukemia research
title_full Advances in culture methods for acute myeloid leukemia research
title_fullStr Advances in culture methods for acute myeloid leukemia research
title_full_unstemmed Advances in culture methods for acute myeloid leukemia research
title_short Advances in culture methods for acute myeloid leukemia research
title_sort advances in culture methods for acute myeloid leukemia research
topic Research Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336936/
https://www.ncbi.nlm.nih.gov/pubmed/34368398
http://dx.doi.org/10.18632/oncoscience.540
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