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Targeting the epichaperome as an effective precision medicine approach in a novel PML-SYK fusion acute myeloid leukemia
The epichaperome is a new cancer target composed of hyperconnected networks of chaperome members that facilitate cell survival. Cancers with an altered chaperone configuration may be susceptible to epichaperome inhibitors. We developed a flow cytometry-based assay for evaluation and monitoring of ep...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155064/ https://www.ncbi.nlm.nih.gov/pubmed/34040147 http://dx.doi.org/10.1038/s41698-021-00183-2 |
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author | Sugita, Mayumi Wilkes, David C. Bareja, Rohan Eng, Kenneth W. Nataraj, Sarah Jimenez-Flores, Reyna A. Yan, LunBiao De Leon, Jeanne Pauline Croyle, Jaclyn A. Kaner, Justin Merugu, Swathi Sharma, Sahil MacDonald, Theresa Y. Noorzad, Zohal Panchal, Palak Pancirer, Danielle Cheng, Shuhua Xiang, Jenny Z. Olson, Luke Van Besien, Koen Rickman, David S. Mathew, Susan Tam, Wayne Rubin, Mark A. Beltran, Himisha Sboner, Andrea Hassane, Duane C. Chiosis, Gabriela Elemento, Olivier Roboz, Gail J. Mosquera, Juan Miguel Guzman, Monica L. |
author_facet | Sugita, Mayumi Wilkes, David C. Bareja, Rohan Eng, Kenneth W. Nataraj, Sarah Jimenez-Flores, Reyna A. Yan, LunBiao De Leon, Jeanne Pauline Croyle, Jaclyn A. Kaner, Justin Merugu, Swathi Sharma, Sahil MacDonald, Theresa Y. Noorzad, Zohal Panchal, Palak Pancirer, Danielle Cheng, Shuhua Xiang, Jenny Z. Olson, Luke Van Besien, Koen Rickman, David S. Mathew, Susan Tam, Wayne Rubin, Mark A. Beltran, Himisha Sboner, Andrea Hassane, Duane C. Chiosis, Gabriela Elemento, Olivier Roboz, Gail J. Mosquera, Juan Miguel Guzman, Monica L. |
author_sort | Sugita, Mayumi |
collection | PubMed |
description | The epichaperome is a new cancer target composed of hyperconnected networks of chaperome members that facilitate cell survival. Cancers with an altered chaperone configuration may be susceptible to epichaperome inhibitors. We developed a flow cytometry-based assay for evaluation and monitoring of epichaperome abundance at the single cell level, with the goal of prospectively identifying patients likely to respond to epichaperome inhibitors, to measure target engagement, and dependency during treatment. As proof of principle, we describe a patient with an unclassified myeloproliferative neoplasm harboring a novel PML-SYK fusion, who progressed to acute myeloid leukemia despite chemotherapy and allogeneic stem cell transplant. The leukemia was identified as having high epichaperome abundance. We obtained compassionate access to an investigational epichaperome inhibitor, PU-H71. After 16 doses, the patient achieved durable complete remission. These encouraging results suggest that further investigation of epichaperome inhibitors in patients with abundant baseline epichaperome levels is warranted. |
format | Online Article Text |
id | pubmed-8155064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81550642021-06-10 Targeting the epichaperome as an effective precision medicine approach in a novel PML-SYK fusion acute myeloid leukemia Sugita, Mayumi Wilkes, David C. Bareja, Rohan Eng, Kenneth W. Nataraj, Sarah Jimenez-Flores, Reyna A. Yan, LunBiao De Leon, Jeanne Pauline Croyle, Jaclyn A. Kaner, Justin Merugu, Swathi Sharma, Sahil MacDonald, Theresa Y. Noorzad, Zohal Panchal, Palak Pancirer, Danielle Cheng, Shuhua Xiang, Jenny Z. Olson, Luke Van Besien, Koen Rickman, David S. Mathew, Susan Tam, Wayne Rubin, Mark A. Beltran, Himisha Sboner, Andrea Hassane, Duane C. Chiosis, Gabriela Elemento, Olivier Roboz, Gail J. Mosquera, Juan Miguel Guzman, Monica L. NPJ Precis Oncol Article The epichaperome is a new cancer target composed of hyperconnected networks of chaperome members that facilitate cell survival. Cancers with an altered chaperone configuration may be susceptible to epichaperome inhibitors. We developed a flow cytometry-based assay for evaluation and monitoring of epichaperome abundance at the single cell level, with the goal of prospectively identifying patients likely to respond to epichaperome inhibitors, to measure target engagement, and dependency during treatment. As proof of principle, we describe a patient with an unclassified myeloproliferative neoplasm harboring a novel PML-SYK fusion, who progressed to acute myeloid leukemia despite chemotherapy and allogeneic stem cell transplant. The leukemia was identified as having high epichaperome abundance. We obtained compassionate access to an investigational epichaperome inhibitor, PU-H71. After 16 doses, the patient achieved durable complete remission. These encouraging results suggest that further investigation of epichaperome inhibitors in patients with abundant baseline epichaperome levels is warranted. Nature Publishing Group UK 2021-05-26 /pmc/articles/PMC8155064/ /pubmed/34040147 http://dx.doi.org/10.1038/s41698-021-00183-2 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sugita, Mayumi Wilkes, David C. Bareja, Rohan Eng, Kenneth W. Nataraj, Sarah Jimenez-Flores, Reyna A. Yan, LunBiao De Leon, Jeanne Pauline Croyle, Jaclyn A. Kaner, Justin Merugu, Swathi Sharma, Sahil MacDonald, Theresa Y. Noorzad, Zohal Panchal, Palak Pancirer, Danielle Cheng, Shuhua Xiang, Jenny Z. Olson, Luke Van Besien, Koen Rickman, David S. Mathew, Susan Tam, Wayne Rubin, Mark A. Beltran, Himisha Sboner, Andrea Hassane, Duane C. Chiosis, Gabriela Elemento, Olivier Roboz, Gail J. Mosquera, Juan Miguel Guzman, Monica L. Targeting the epichaperome as an effective precision medicine approach in a novel PML-SYK fusion acute myeloid leukemia |
title | Targeting the epichaperome as an effective precision medicine approach in a novel PML-SYK fusion acute myeloid leukemia |
title_full | Targeting the epichaperome as an effective precision medicine approach in a novel PML-SYK fusion acute myeloid leukemia |
title_fullStr | Targeting the epichaperome as an effective precision medicine approach in a novel PML-SYK fusion acute myeloid leukemia |
title_full_unstemmed | Targeting the epichaperome as an effective precision medicine approach in a novel PML-SYK fusion acute myeloid leukemia |
title_short | Targeting the epichaperome as an effective precision medicine approach in a novel PML-SYK fusion acute myeloid leukemia |
title_sort | targeting the epichaperome as an effective precision medicine approach in a novel pml-syk fusion acute myeloid leukemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155064/ https://www.ncbi.nlm.nih.gov/pubmed/34040147 http://dx.doi.org/10.1038/s41698-021-00183-2 |
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