The spatial landscape of cancer hallmarks reveals patterns of tumor ecological dynamics and drug sensitivity

被引:2
作者
Sibai, Mustafa [1 ,2 ]
Cervilla, Sergi [1 ]
Grases, Daniela [1 ]
Musulen, Eva [1 ,3 ]
Lazcano, Rossana [4 ]
Mo, Chia-Kuei [5 ]
Davalos, Veronica [1 ]
Fortian, Arola [6 ]
Bernat, Adria [6 ]
Romeo, Margarita [6 ]
Tokheim, Collin [7 ]
Barretina, Jordi [6 ]
Lazar, Alexander J. [4 ]
Ding, Li [5 ]
Grande, Enrique [8 ]
Real, Francisco X. [9 ,10 ,11 ]
Esteller, Manel [1 ,10 ,12 ,13 ]
Bailey, Matthew H. [14 ,15 ]
Porta-Pardo, Eduard [1 ,2 ]
机构
[1] Josep Carreras Leukaemia Res Inst IJC, Badalona, Spain
[2] Barcelona Supercomp Ctr BSC, Barcelona, Spain
[3] Hosp Univ Gen Catalunya, Dept Neurol, Grp QuironSalud, Sant Cugat Del Valles, Spain
[4] Univ Texas MD Anderson Canc Ctr, Houston, TX USA
[5] Washington Univ St Louis, Dept Med & Genet, Siteman Canc Ctr, St Louis, MO USA
[6] Inst Recerca Germans Trias I Pujol HUGTP IGTP, Badalona, Spain
[7] Dana Farber Canc Inst, Dept Data Sci, Boston, MA USA
[8] MD Anderson Canc Ctr Madrid, Dept Med Oncol, Madrid, Spain
[9] Ctr Nacl Invest Oncol CNIO, Madrid, Spain
[10] Ctr Invest Biomed Red Canc CIBERONC, Madrid, Spain
[11] Univ Pompeu Fabra, Dept Med & Life Sci, Barcelona, Spain
[12] Inst Catalana Recerca & Estudis Avancats ICREA, Barcelona, Spain
[13] Univ Barcelona, Physiol Sci Dept, Sch Med & Hlth Sci, Barcelona, Catalonia, Spain
[14] Brigham Young Univ, Dept Biol, Provo, UT 84602 USA
[15] Brigham Young Univ, Simmons Ctr Canc Res, Provo, UT USA
关键词
SINGLE-CELL; ATLAS;
D O I
10.1016/j.celrep.2024.115229
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页数:22
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