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Implantation of engineered adipocytes that outcompete tumors for resources suppresses cancer progression
Tumors acquire an increased ability to obtain and metabolize nutrients. Here, we engineered and implanted adipocytes to outcompete tumors for nutrients and show that they can substantially reduce cancer progression. Growing cells or xenografts from several cancers (breast, colon, pancreas, prostate)...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081280/ https://www.ncbi.nlm.nih.gov/pubmed/37034710 http://dx.doi.org/10.1101/2023.03.28.534564 |
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author | Nguyen, Hai P. Sheng, Rory Murray, Elizabeth Ito, Yusuke Bruck, Michael Biellak, Cassidy An, Kelly Lynce, Filipa Dillon, Deborah A. Magbanua, Mark Jesus M. Huppert, Laura A. Hammerlindl, Heinz Esserman, Laura Rosenbluth, Jennifer M. Ahituv, Nadav |
author_facet | Nguyen, Hai P. Sheng, Rory Murray, Elizabeth Ito, Yusuke Bruck, Michael Biellak, Cassidy An, Kelly Lynce, Filipa Dillon, Deborah A. Magbanua, Mark Jesus M. Huppert, Laura A. Hammerlindl, Heinz Esserman, Laura Rosenbluth, Jennifer M. Ahituv, Nadav |
author_sort | Nguyen, Hai P. |
collection | PubMed |
description | Tumors acquire an increased ability to obtain and metabolize nutrients. Here, we engineered and implanted adipocytes to outcompete tumors for nutrients and show that they can substantially reduce cancer progression. Growing cells or xenografts from several cancers (breast, colon, pancreas, prostate) alongside engineered human adipocytes or adipose organoids significantly suppresses cancer progression and reduces hypoxia and angiogenesis. Transplanting modulated adipocyte organoids in pancreatic or breast cancer mouse models nearby or distal from the tumor significantly suppresses its growth. To further showcase therapeutic potential, we demonstrate that co-culturing tumor organoids derived from human breast cancers with engineered patient-derived adipocytes significantly reduces cancer growth. Combined, our results introduce a novel cancer therapeutic approach, termed adipose modulation transplantation (AMT), that can be utilized for a broad range of cancers. |
format | Online Article Text |
id | pubmed-10081280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100812802023-04-08 Implantation of engineered adipocytes that outcompete tumors for resources suppresses cancer progression Nguyen, Hai P. Sheng, Rory Murray, Elizabeth Ito, Yusuke Bruck, Michael Biellak, Cassidy An, Kelly Lynce, Filipa Dillon, Deborah A. Magbanua, Mark Jesus M. Huppert, Laura A. Hammerlindl, Heinz Esserman, Laura Rosenbluth, Jennifer M. Ahituv, Nadav bioRxiv Article Tumors acquire an increased ability to obtain and metabolize nutrients. Here, we engineered and implanted adipocytes to outcompete tumors for nutrients and show that they can substantially reduce cancer progression. Growing cells or xenografts from several cancers (breast, colon, pancreas, prostate) alongside engineered human adipocytes or adipose organoids significantly suppresses cancer progression and reduces hypoxia and angiogenesis. Transplanting modulated adipocyte organoids in pancreatic or breast cancer mouse models nearby or distal from the tumor significantly suppresses its growth. To further showcase therapeutic potential, we demonstrate that co-culturing tumor organoids derived from human breast cancers with engineered patient-derived adipocytes significantly reduces cancer growth. Combined, our results introduce a novel cancer therapeutic approach, termed adipose modulation transplantation (AMT), that can be utilized for a broad range of cancers. Cold Spring Harbor Laboratory 2023-03-29 /pmc/articles/PMC10081280/ /pubmed/37034710 http://dx.doi.org/10.1101/2023.03.28.534564 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Nguyen, Hai P. Sheng, Rory Murray, Elizabeth Ito, Yusuke Bruck, Michael Biellak, Cassidy An, Kelly Lynce, Filipa Dillon, Deborah A. Magbanua, Mark Jesus M. Huppert, Laura A. Hammerlindl, Heinz Esserman, Laura Rosenbluth, Jennifer M. Ahituv, Nadav Implantation of engineered adipocytes that outcompete tumors for resources suppresses cancer progression |
title | Implantation of engineered adipocytes that outcompete tumors for resources suppresses cancer progression |
title_full | Implantation of engineered adipocytes that outcompete tumors for resources suppresses cancer progression |
title_fullStr | Implantation of engineered adipocytes that outcompete tumors for resources suppresses cancer progression |
title_full_unstemmed | Implantation of engineered adipocytes that outcompete tumors for resources suppresses cancer progression |
title_short | Implantation of engineered adipocytes that outcompete tumors for resources suppresses cancer progression |
title_sort | implantation of engineered adipocytes that outcompete tumors for resources suppresses cancer progression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081280/ https://www.ncbi.nlm.nih.gov/pubmed/37034710 http://dx.doi.org/10.1101/2023.03.28.534564 |
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