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Spatially aware deep learning reveals tumor heterogeneity patterns that encode distinct kidney cancer states

Clear cell renal cell carcinoma (ccRCC) is molecularly heterogeneous, immune infiltrated, and selectively sensitive to immune checkpoint inhibition (ICI). However, the joint tumor-immune states that mediate ICI response remain elusive. We develop spatially aware deep-learning models of tumor and imm...

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Autores principales: Nyman, Jackson, Denize, Thomas, Bakouny, Ziad, Labaki, Chris, Titchen, Breanna M., Bi, Kevin, Hari, Surya Narayanan, Rosenthal, Jacob, Mehta, Nicita, Jiang, Bowen, Sharma, Bijaya, Felt, Kristen, Umeton, Renato, Braun, David A., Rodig, Scott, Choueiri, Toni K., Signoretti, Sabina, Van Allen, Eliezer M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518628/
https://www.ncbi.nlm.nih.gov/pubmed/37729872
http://dx.doi.org/10.1016/j.xcrm.2023.101189
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author Nyman, Jackson
Denize, Thomas
Bakouny, Ziad
Labaki, Chris
Titchen, Breanna M.
Bi, Kevin
Hari, Surya Narayanan
Rosenthal, Jacob
Mehta, Nicita
Jiang, Bowen
Sharma, Bijaya
Felt, Kristen
Umeton, Renato
Braun, David A.
Rodig, Scott
Choueiri, Toni K.
Signoretti, Sabina
Van Allen, Eliezer M.
author_facet Nyman, Jackson
Denize, Thomas
Bakouny, Ziad
Labaki, Chris
Titchen, Breanna M.
Bi, Kevin
Hari, Surya Narayanan
Rosenthal, Jacob
Mehta, Nicita
Jiang, Bowen
Sharma, Bijaya
Felt, Kristen
Umeton, Renato
Braun, David A.
Rodig, Scott
Choueiri, Toni K.
Signoretti, Sabina
Van Allen, Eliezer M.
author_sort Nyman, Jackson
collection PubMed
description Clear cell renal cell carcinoma (ccRCC) is molecularly heterogeneous, immune infiltrated, and selectively sensitive to immune checkpoint inhibition (ICI). However, the joint tumor-immune states that mediate ICI response remain elusive. We develop spatially aware deep-learning models of tumor and immune features to learn representations of ccRCC tumors using diagnostic whole-slide images (WSIs) in untreated and treated contexts (n = 1,102 patients). We identify patterns of grade heterogeneity in WSIs not achievable through human pathologist analysis, and these graph-based “microheterogeneity” structures associate with PBRM1 loss of function and with patient outcomes. Joint analysis of tumor phenotypes and immune infiltration identifies a subpopulation of highly infiltrated, microheterogeneous tumors responsive to ICI. In paired multiplex immunofluorescence images of ccRCC, microheterogeneity associates with greater PD1 activation in CD8(+) lymphocytes and increased tumor-immune interactions. Our work reveals spatially interacting tumor-immune structures underlying ccRCC biology that may also inform selective response to ICI.
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spelling pubmed-105186282023-09-26 Spatially aware deep learning reveals tumor heterogeneity patterns that encode distinct kidney cancer states Nyman, Jackson Denize, Thomas Bakouny, Ziad Labaki, Chris Titchen, Breanna M. Bi, Kevin Hari, Surya Narayanan Rosenthal, Jacob Mehta, Nicita Jiang, Bowen Sharma, Bijaya Felt, Kristen Umeton, Renato Braun, David A. Rodig, Scott Choueiri, Toni K. Signoretti, Sabina Van Allen, Eliezer M. Cell Rep Med Article Clear cell renal cell carcinoma (ccRCC) is molecularly heterogeneous, immune infiltrated, and selectively sensitive to immune checkpoint inhibition (ICI). However, the joint tumor-immune states that mediate ICI response remain elusive. We develop spatially aware deep-learning models of tumor and immune features to learn representations of ccRCC tumors using diagnostic whole-slide images (WSIs) in untreated and treated contexts (n = 1,102 patients). We identify patterns of grade heterogeneity in WSIs not achievable through human pathologist analysis, and these graph-based “microheterogeneity” structures associate with PBRM1 loss of function and with patient outcomes. Joint analysis of tumor phenotypes and immune infiltration identifies a subpopulation of highly infiltrated, microheterogeneous tumors responsive to ICI. In paired multiplex immunofluorescence images of ccRCC, microheterogeneity associates with greater PD1 activation in CD8(+) lymphocytes and increased tumor-immune interactions. Our work reveals spatially interacting tumor-immune structures underlying ccRCC biology that may also inform selective response to ICI. Elsevier 2023-09-19 /pmc/articles/PMC10518628/ /pubmed/37729872 http://dx.doi.org/10.1016/j.xcrm.2023.101189 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Nyman, Jackson
Denize, Thomas
Bakouny, Ziad
Labaki, Chris
Titchen, Breanna M.
Bi, Kevin
Hari, Surya Narayanan
Rosenthal, Jacob
Mehta, Nicita
Jiang, Bowen
Sharma, Bijaya
Felt, Kristen
Umeton, Renato
Braun, David A.
Rodig, Scott
Choueiri, Toni K.
Signoretti, Sabina
Van Allen, Eliezer M.
Spatially aware deep learning reveals tumor heterogeneity patterns that encode distinct kidney cancer states
title Spatially aware deep learning reveals tumor heterogeneity patterns that encode distinct kidney cancer states
title_full Spatially aware deep learning reveals tumor heterogeneity patterns that encode distinct kidney cancer states
title_fullStr Spatially aware deep learning reveals tumor heterogeneity patterns that encode distinct kidney cancer states
title_full_unstemmed Spatially aware deep learning reveals tumor heterogeneity patterns that encode distinct kidney cancer states
title_short Spatially aware deep learning reveals tumor heterogeneity patterns that encode distinct kidney cancer states
title_sort spatially aware deep learning reveals tumor heterogeneity patterns that encode distinct kidney cancer states
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518628/
https://www.ncbi.nlm.nih.gov/pubmed/37729872
http://dx.doi.org/10.1016/j.xcrm.2023.101189
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