Molecular determinants of response to PD-L1 blockade across tumor types
PD-L1 immune checkpoint inhibition has been used for several tumour types. Here, the authors use immunohistochemistry, tumour mutation burden and RNA-seq data from 366 patients with different indications to identify molecular signatures of response to atezolizumab and reveal pathway heterogeneity an...
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2021-06-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-021-24112-w |
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doaj-ae29efdfced64f11b4172bdb2e1a8bde2021-06-27T11:12:46ZengNature Publishing GroupNature Communications2041-17232021-06-0112111110.1038/s41467-021-24112-wMolecular determinants of response to PD-L1 blockade across tumor typesRomain Banchereau0Ning Leng1Oliver Zill2Ethan Sokol3Gengbo Liu4Dean Pavlick5Sophia Maund6Li-Fen Liu7Edward Kadel8Nicole Baldwin9Suchit Jhunjhunwala10Dorothee Nickles11Zoe June Assaf12Daniel Bower13Namrata Patil14Mark McCleland15David Shames16Luciana Molinero17Mahrukh Huseni18Shomyseh Sanjabi19Craig Cummings20Ira Mellman21Sanjeev Mariathasan22Priti Hegde23Thomas Powles24GenentechGenentechGenentechFoundation MedicineGenentechFoundation MedicineGenentechGenentechGenentechBaylor Institute for Immunology ResearchGenentechGenentechGenentechGenentechGenentechGenentechGenentechGenentechGenentechGenentechGenentechGenentechGenentechFoundation MedicineBarts Experimental Cancer Medicine Centre, Barts Cancer Institute, Queen Mary University of LondonPD-L1 immune checkpoint inhibition has been used for several tumour types. Here, the authors use immunohistochemistry, tumour mutation burden and RNA-seq data from 366 patients with different indications to identify molecular signatures of response to atezolizumab and reveal pathway heterogeneity and the involvement of non-immune pathways.https://doi.org/10.1038/s41467-021-24112-w |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Romain Banchereau Ning Leng Oliver Zill Ethan Sokol Gengbo Liu Dean Pavlick Sophia Maund Li-Fen Liu Edward Kadel Nicole Baldwin Suchit Jhunjhunwala Dorothee Nickles Zoe June Assaf Daniel Bower Namrata Patil Mark McCleland David Shames Luciana Molinero Mahrukh Huseni Shomyseh Sanjabi Craig Cummings Ira Mellman Sanjeev Mariathasan Priti Hegde Thomas Powles |
spellingShingle |
Romain Banchereau Ning Leng Oliver Zill Ethan Sokol Gengbo Liu Dean Pavlick Sophia Maund Li-Fen Liu Edward Kadel Nicole Baldwin Suchit Jhunjhunwala Dorothee Nickles Zoe June Assaf Daniel Bower Namrata Patil Mark McCleland David Shames Luciana Molinero Mahrukh Huseni Shomyseh Sanjabi Craig Cummings Ira Mellman Sanjeev Mariathasan Priti Hegde Thomas Powles Molecular determinants of response to PD-L1 blockade across tumor types Nature Communications |
author_facet |
Romain Banchereau Ning Leng Oliver Zill Ethan Sokol Gengbo Liu Dean Pavlick Sophia Maund Li-Fen Liu Edward Kadel Nicole Baldwin Suchit Jhunjhunwala Dorothee Nickles Zoe June Assaf Daniel Bower Namrata Patil Mark McCleland David Shames Luciana Molinero Mahrukh Huseni Shomyseh Sanjabi Craig Cummings Ira Mellman Sanjeev Mariathasan Priti Hegde Thomas Powles |
author_sort |
Romain Banchereau |
title |
Molecular determinants of response to PD-L1 blockade across tumor types |
title_short |
Molecular determinants of response to PD-L1 blockade across tumor types |
title_full |
Molecular determinants of response to PD-L1 blockade across tumor types |
title_fullStr |
Molecular determinants of response to PD-L1 blockade across tumor types |
title_full_unstemmed |
Molecular determinants of response to PD-L1 blockade across tumor types |
title_sort |
molecular determinants of response to pd-l1 blockade across tumor types |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2021-06-01 |
description |
PD-L1 immune checkpoint inhibition has been used for several tumour types. Here, the authors use immunohistochemistry, tumour mutation burden and RNA-seq data from 366 patients with different indications to identify molecular signatures of response to atezolizumab and reveal pathway heterogeneity and the involvement of non-immune pathways. |
url |
https://doi.org/10.1038/s41467-021-24112-w |
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