TY - JOUR
T1 - Single-cell transcriptomics and epigenomics unravel the role of monocytes in neuroblastoma bone marrow metastasis
AU - Fetahu, Irfete S.
AU - Esser-Skala, Wolfgang
AU - Dnyansagar, Rohit
AU - Sindelar, Samuel
AU - Rifatbegovic, Fikret
AU - Bileck, Andrea
AU - Skos, Lukas
AU - Bozsaky, Eva
AU - Lazic, Daria
AU - Shaw, Lisa
AU - Tötzl, Marcus
AU - Tarlungeanu, Dora
AU - Bernkopf, Marie
AU - Rados, Magdalena
AU - Weninger, Wolfgang
AU - Tomazou, Eleni M.
AU - Bock, Christoph
AU - Gerner, Christopher
AU - Ladenstein, Ruth
AU - Farlik, Matthias
AU - Fortelny, Nikolaus
AU - Taschner-Mandl, Sabine
N1 - Accession Number: WOS:001017010300013
PubMed ID: 37365178
PY - 2023/12
Y1 - 2023/12
N2 - Metastasis is the major cause of cancer-related deaths. Neuroblastoma (NB), a childhood tumor has been molecularly defined at the primary cancer site, however, the bone marrow (BM) as the metastatic niche of NB is poorly characterized. Here we perform single-cell transcriptomic and epigenomic profiling of BM aspirates from 11 subjects spanning three major NB subtypes and compare these to five age-matched and metastasis-free BM, followed by in-depth single cell analyses of tissue diversity and cell-cell interactions, as well as functional validation. We show that cellular plasticity of NB tumor cells is conserved upon metastasis and tumor cell type composition is NB subtype-dependent. NB cells signal to the BM microenvironment, rewiring via macrophage mgration inhibitory factor and midkine signaling specifically monocytes, which exhibit M1 and M2 features, are marked by activation of pro- and anti-inflammatory programs, and express tumor-promoting factors, reminiscent of tumor-associated macrophages. The interactions and pathways characterized in our study provide the basis for therapeutic approaches that target tumor-to-microenvironment interactions.
AB - Metastasis is the major cause of cancer-related deaths. Neuroblastoma (NB), a childhood tumor has been molecularly defined at the primary cancer site, however, the bone marrow (BM) as the metastatic niche of NB is poorly characterized. Here we perform single-cell transcriptomic and epigenomic profiling of BM aspirates from 11 subjects spanning three major NB subtypes and compare these to five age-matched and metastasis-free BM, followed by in-depth single cell analyses of tissue diversity and cell-cell interactions, as well as functional validation. We show that cellular plasticity of NB tumor cells is conserved upon metastasis and tumor cell type composition is NB subtype-dependent. NB cells signal to the BM microenvironment, rewiring via macrophage mgration inhibitory factor and midkine signaling specifically monocytes, which exhibit M1 and M2 features, are marked by activation of pro- and anti-inflammatory programs, and express tumor-promoting factors, reminiscent of tumor-associated macrophages. The interactions and pathways characterized in our study provide the basis for therapeutic approaches that target tumor-to-microenvironment interactions.
UR - http://www.scopus.com/inward/record.url?scp=85163333321&partnerID=8YFLogxK
U2 - 10.1038/s41467-023-39210-0
DO - 10.1038/s41467-023-39210-0
M3 - Article
C2 - 37365178
AN - SCOPUS:85163333321
VL - 14
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
IS - 1
M1 - 3620
ER -