Bill, Ruben; Wirapati, Pratyaksha; Messemaker, Marius; Roh, Whijae; Zitti, Beatrice; Duval, Florent; Kiss, Máté; Park, Jong Chul; Saal, Talia M; Hoelzl, Jan; Tarussio, David; Benedetti, Fabrizio; Tissot, Stéphanie; Kandalaft, Lana; Varrone, Marco; Ciriello, Giovanni; McKee, Thomas A; Monnier, Yan; Mermod, Maxime; Blaum, Emily M; ... (2023). CXCL9:SPP1 macrophage polarity identifies a network of cellular programs that control human cancers. Science, 381(6657), pp. 515-524. American Association for the Advancement of Science 10.1126/science.ade2292
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Tumor microenvironments (TMEs) influence cancer progression but are complex and often differ between patients. Considering that microenvironment variations may reveal rules governing intratumoral cellular programs and disease outcome, we focused on tumor-to-tumor variation to examine 52 head and neck squamous cell carcinomas. We found that macrophage polarity-defined by CXCL9 and SPP1 (CS) expression but not by conventional M1 and M2 markers-had a noticeably strong prognostic association. CS macrophage polarity also identified a highly coordinated network of either pro- or antitumor variables, which involved each tumor-associated cell type and was spatially organized. We extended these findings to other cancer indications. Overall, these results suggest that, despite their complexity, TMEs coordinate coherent responses that control human cancers and for which CS macrophage polarity is a relevant yet simple variable.
Item Type: |
Journal Article (Original Article) |
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Division/Institute: |
04 Faculty of Medicine > Department of Haematology, Oncology, Infectious Diseases, Laboratory Medicine and Hospital Pharmacy (DOLS) > Clinic of Medical Oncology |
UniBE Contributor: |
Bill, Ruben |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
1095-9203 |
Publisher: |
American Association for the Advancement of Science |
Language: |
English |
Submitter: |
Pubmed Import |
Date Deposited: |
04 Aug 2023 09:34 |
Last Modified: |
05 Aug 2023 15:27 |
Publisher DOI: |
10.1126/science.ade2292 |
PubMed ID: |
37535729 |
BORIS DOI: |
10.48350/185211 |
URI: |
https://boris.unibe.ch/id/eprint/185211 |