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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9380677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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