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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)...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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.
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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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