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Application of immune enhanced organoids in modeling personalized Merkel cell carcinoma research

Merkel cell carcinoma (MCC) is a rare neuroendocrine cutaneous cancer, with incidence of less than 1/100,000, low survival rates and variable response to chemotherapy or immunotherapy. Herein we explore the application of patient tumor organoids (PTOs) in modeling personalized research in this rare...

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Autores principales: Forsythe, Steven D., Erali, Richard A., Laney, Preston, Sivakumar, Hemamylammal, Li, Wencheng, Skardal, Aleksander, Soker, Shay, Votanopoulos, Konstantinos I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380677/
https://www.ncbi.nlm.nih.gov/pubmed/35974123
http://dx.doi.org/10.1038/s41598-022-17921-6
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author Forsythe, Steven D.
Erali, Richard A.
Laney, Preston
Sivakumar, Hemamylammal
Li, Wencheng
Skardal, Aleksander
Soker, Shay
Votanopoulos, Konstantinos I.
author_facet Forsythe, Steven D.
Erali, Richard A.
Laney, Preston
Sivakumar, Hemamylammal
Li, Wencheng
Skardal, Aleksander
Soker, Shay
Votanopoulos, Konstantinos I.
author_sort Forsythe, Steven D.
collection PubMed
description Merkel cell carcinoma (MCC) is a rare neuroendocrine cutaneous cancer, with incidence of less than 1/100,000, low survival rates and variable response to chemotherapy or immunotherapy. Herein we explore the application of patient tumor organoids (PTOs) in modeling personalized research in this rare malignancy. Unsorted and non-expanded MCC tumor cells were isolated from surgical specimens and suspended in an ECM based hydrogel, along with patient matched blood and lymph node tissue to generate immune enhanced organoids (iPTOs). Organoids were treated with chemotherapy or immunotherapy agents and efficacy was determined by post-treatment viability. Nine specimens from seven patients were recruited from December 2018-January 2022. Establishment rate was 88.8% (8/9) for PTOs and 77.8% (7/9) for iPTOs. Histology on matched patient tissues and PTOs demonstrated expression of MCC markers. Chemotherapy response was exhibited in 4/6 (66.6%) specimens with cisplatin and doxorubicin as the most effective agents (4/6 PTO sets) while immunotherapy was not effective in tested iPTO sets. Four specimens from two patients demonstrated resistance to pembrolizumab, correlating with the corresponding patient’s treatment response. Routine establishment and immune enhancement of MCC PTOs is feasible directly from resected surgical specimens allowing for personalized research and exploration of treatment regimens in the preclinical setting.
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spelling pubmed-93806772022-08-17 Application of immune enhanced organoids in modeling personalized Merkel cell carcinoma research Forsythe, Steven D. Erali, Richard A. Laney, Preston Sivakumar, Hemamylammal Li, Wencheng Skardal, Aleksander Soker, Shay Votanopoulos, Konstantinos I. Sci Rep Article Merkel cell carcinoma (MCC) is a rare neuroendocrine cutaneous cancer, with incidence of less than 1/100,000, low survival rates and variable response to chemotherapy or immunotherapy. Herein we explore the application of patient tumor organoids (PTOs) in modeling personalized research in this rare malignancy. Unsorted and non-expanded MCC tumor cells were isolated from surgical specimens and suspended in an ECM based hydrogel, along with patient matched blood and lymph node tissue to generate immune enhanced organoids (iPTOs). Organoids were treated with chemotherapy or immunotherapy agents and efficacy was determined by post-treatment viability. Nine specimens from seven patients were recruited from December 2018-January 2022. Establishment rate was 88.8% (8/9) for PTOs and 77.8% (7/9) for iPTOs. Histology on matched patient tissues and PTOs demonstrated expression of MCC markers. Chemotherapy response was exhibited in 4/6 (66.6%) specimens with cisplatin and doxorubicin as the most effective agents (4/6 PTO sets) while immunotherapy was not effective in tested iPTO sets. Four specimens from two patients demonstrated resistance to pembrolizumab, correlating with the corresponding patient’s treatment response. Routine establishment and immune enhancement of MCC PTOs is feasible directly from resected surgical specimens allowing for personalized research and exploration of treatment regimens in the preclinical setting. Nature Publishing Group UK 2022-08-16 /pmc/articles/PMC9380677/ /pubmed/35974123 http://dx.doi.org/10.1038/s41598-022-17921-6 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Forsythe, Steven D.
Erali, Richard A.
Laney, Preston
Sivakumar, Hemamylammal
Li, Wencheng
Skardal, Aleksander
Soker, Shay
Votanopoulos, Konstantinos I.
Application of immune enhanced organoids in modeling personalized Merkel cell carcinoma research
title Application of immune enhanced organoids in modeling personalized Merkel cell carcinoma research
title_full Application of immune enhanced organoids in modeling personalized Merkel cell carcinoma research
title_fullStr Application of immune enhanced organoids in modeling personalized Merkel cell carcinoma research
title_full_unstemmed Application of immune enhanced organoids in modeling personalized Merkel cell carcinoma research
title_short Application of immune enhanced organoids in modeling personalized Merkel cell carcinoma research
title_sort application of immune enhanced organoids in modeling personalized merkel cell carcinoma research
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380677/
https://www.ncbi.nlm.nih.gov/pubmed/35974123
http://dx.doi.org/10.1038/s41598-022-17921-6
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