Unbiased niche labeling maps immune-excluded niche in bone metastasis
Summary
Metastatic cancer cell fate is shaped by the local microenvironment niches. To unbiasedly define the cellular and molecular features of metastatic niches, we developed sortase A-based microenvironment niche tagging (SAMENT), which selectively labels cells encountered by cancer cells during metastasis. Applying SAMENT across multiple cancer models and target organs revealed shared niche features, including macrophage enrichment and T cell depletion, alongside marked organ-specific phenotype
Content
# Unbiased niche labeling maps immune-excluded niche in bone metastasis
*Published: 2026 Apr 28*
Metastatic cancer cell fate is shaped by the local microenvironment niches. To
unbiasedly define the cellular and molecular features of metastatic niches, we
developed sortase A-based microenvironment niche tagging (SAMENT), which
selectively labels cells encountered by cancer cells during metastasis. Applying
SAMENT across multiple cancer models and target organs revealed shared niche
features, including macrophage enrichment and T cell depletion, alongside marked
organ-specific phenotype heterogeneity in niche macrophages. In bone, metastatic
niches are enriched for macrophages expressing estrogen receptor alpha (ERα)
with active ERα signaling. Conditional deletion of Esr1 in macrophages
significantly impaired bone colonization by enabling T cell infiltration. ERα⁺
macrophages were also identified in human bone metastases across multiple cancer
types. Together, these findings define a distinct ERα⁺ macrophage niche and
establish macrophage ERα signaling as a key driver of T cell exclusion during
metastatic colonization.
DOI: 10.1016/j.cell.2026.04.009