TY - JOUR
T1 - The spatial landscape of cancer hallmarks reveals patterns of tumor ecological dynamics and drug sensitivity
AU - the DUTRENEO Study Investigators
AU - Sibai, Mustafa
AU - Cervilla, Sergi
AU - Grases, Daniela
AU - Musulen, Eva
AU - Lazcano, Rossana
AU - Mo, Chia Kuei
AU - Davalos, Veronica
AU - Fortian, Arola
AU - Bernat, Adrià
AU - Romeo, Margarita
AU - Tokheim, Collin
AU - Barretina, Jordi
AU - Lazar, Alexander J.
AU - Ding, Li
AU - Grande, Enrique
AU - Alonso-Gordoa, Teresa
AU - Álvarez-Maestro, Mario
AU - Andrada, Elena
AU - Azueta, Ainara
AU - Javier Burgos, Raquel Benítez
AU - Castellano, Daniel
AU - Climent, M. Angel
AU - Domínguez, Mario
AU - Albert Font, Ignacio Durán
AU - Galante, Isabel
AU - Galván, Patricia
AU - García, Juan F.
AU - García del Muro, Xavier
AU - Guerrero-Ramos, Félix
AU - Malats, Núria
AU - Marqués, Miriam
AU - Maroto, Pablo
AU - Martínez de Villarreal, Jaime
AU - Moreno-Oya, Ane
AU - Paramio, Jesús M.
AU - Pinto, Alvaro
AU - Prat, Aleix
AU - Puente, Javier
AU - Reig, Oscar
AU - Real, Francisco X.
AU - Real, Francisco X.
AU - Esteller, Manel
AU - Bailey, Matthew H.
AU - Porta-Pardo, Eduard
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025/2/25
Y1 - 2025/2/25
N2 - Tumors are complex ecosystems of interacting cell types. The concept of cancer hallmarks distills this complexity into underlying principles that govern tumor growth. Here, we explore the spatial distribution of cancer hallmarks across 63 primary untreated tumors from 10 cancer types using spatial transcriptomics. We show that hallmark activity is spatially organized, with the cancer compartment contributing to the activity of seven out of 13 hallmarks, while the tumor microenvironment (TME) contributes to the activity of the rest. Additionally, we discover that genomic distance between tumor subclones correlates with differences in hallmark activity, even leading to clone-hallmark specialization. Finally, we demonstrate interdependent relationships between hallmarks at the junctions of TME and cancer compartments and how they relate to sensitivity to different neoadjuvant treatments in 33 bladder cancer patients from the DUTRENEO trial. In conclusion, our findings may improve our understanding of tumor ecology and help identify new drug biomarkers.
AB - Tumors are complex ecosystems of interacting cell types. The concept of cancer hallmarks distills this complexity into underlying principles that govern tumor growth. Here, we explore the spatial distribution of cancer hallmarks across 63 primary untreated tumors from 10 cancer types using spatial transcriptomics. We show that hallmark activity is spatially organized, with the cancer compartment contributing to the activity of seven out of 13 hallmarks, while the tumor microenvironment (TME) contributes to the activity of the rest. Additionally, we discover that genomic distance between tumor subclones correlates with differences in hallmark activity, even leading to clone-hallmark specialization. Finally, we demonstrate interdependent relationships between hallmarks at the junctions of TME and cancer compartments and how they relate to sensitivity to different neoadjuvant treatments in 33 bladder cancer patients from the DUTRENEO trial. In conclusion, our findings may improve our understanding of tumor ecology and help identify new drug biomarkers.
KW - CP: cancer
KW - cancer hallmarks
KW - drug sensitivity
KW - ecosystem
KW - intratumoral heterogeneity
KW - spatial transcriptomics
KW - tumor microenvironment
UR - https://www.scopus.com/pages/publications/85216086340
U2 - 10.1016/j.celrep.2024.115229
DO - 10.1016/j.celrep.2024.115229
M3 - Article
C2 - 39864059
AN - SCOPUS:85216086340
SN - 2639-1856
VL - 44
JO - Cell Reports
JF - Cell Reports
IS - 2
M1 - 115229
ER -