TY - JOUR
T1 - Immune Infiltrate and Tumor Microenvironment Transcriptional Programs Stratify Pediatric Osteosarcoma into Prognostic Groups at Diagnosis
AU - Marchais, Antonin
AU - Marques da Costa, Maria Eugenia
AU - Job, Bastien
AU - Abbas, Rachid
AU - Drubay, Damien
AU - Piperno-Neumann, Sophie
AU - Fromigué, Olivia
AU - Gomez-Brouchet, Anne
AU - Redini, Françoise
AU - Droit, Robin
AU - Lervat, Cyril
AU - Entze-Werle, Natacha
AU - Pacquement, Helénè
AU - Devoldere, Catherine
AU - Cupissol, Didier
AU - Bodet, Damien
AU - Gandemer, Virginie
AU - Berger, Marc
AU - Marec-Berard, Perrine
AU - Jimenez, Marta
AU - Vassal, Gilles
AU - Geoerger, Birgit
AU - Brugières, Laurence
AU - Gaspar, Nathalie
N1 - Publisher Copyright:
© 2022 American Association for Cancer Research
PY - 2022/3/15
Y1 - 2022/3/15
N2 - The outcomes of adolescents/young adults with osteosarcoma have not improved in decades. The chaotic karyotype of this rare tumor has precluded the identification of prognostic biomarkers and patient stratification. We reasoned that transcriptomic studies should overcome this genetic complexity. RNA sequencing (RNA-seq) of 79 osteosarcoma diagnostic biopsies identified stable independent components that recapitulate the tumor and microenvironment cell composition. Unsupervised classification of the independent components stratified this cohort into favorable (G1) and unfavorable (G2) prognostic tumors in terms of overall survival. Multivariate survival analysis ranked this stratification as the most influential variable. Functional characterization associated G1 tumors with innate immunity and G2 tumors with angiogenic, osteoclastic, and adipogenic activities as well as PPARg pathway upregulation. A focused gene signature that predicted G1/G2 tumors from RNA-seq data was developed and validated within an independent cohort of 82 osteosarcomas. This signature was further validated with a custom NanoString panel in 96 additional osteosarcomas. This study thus proposes new biomarkers to detect high-risk patients and new therapeutic options for osteosarcoma.
AB - The outcomes of adolescents/young adults with osteosarcoma have not improved in decades. The chaotic karyotype of this rare tumor has precluded the identification of prognostic biomarkers and patient stratification. We reasoned that transcriptomic studies should overcome this genetic complexity. RNA sequencing (RNA-seq) of 79 osteosarcoma diagnostic biopsies identified stable independent components that recapitulate the tumor and microenvironment cell composition. Unsupervised classification of the independent components stratified this cohort into favorable (G1) and unfavorable (G2) prognostic tumors in terms of overall survival. Multivariate survival analysis ranked this stratification as the most influential variable. Functional characterization associated G1 tumors with innate immunity and G2 tumors with angiogenic, osteoclastic, and adipogenic activities as well as PPARg pathway upregulation. A focused gene signature that predicted G1/G2 tumors from RNA-seq data was developed and validated within an independent cohort of 82 osteosarcomas. This signature was further validated with a custom NanoString panel in 96 additional osteosarcomas. This study thus proposes new biomarkers to detect high-risk patients and new therapeutic options for osteosarcoma.
UR - http://www.scopus.com/inward/record.url?scp=85126490702&partnerID=8YFLogxK
U2 - 10.1158/0008-5472.CAN-20-4189
DO - 10.1158/0008-5472.CAN-20-4189
M3 - Article
C2 - 35078815
AN - SCOPUS:85126490702
SN - 0008-5472
VL - 82
SP - 974
EP - 985
JO - Cancer Research
JF - Cancer Research
IS - 6
ER -