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<p>Macrophages are the major immune cell type in the microenvironment of non-small cell lung cancer (NSCLC), playing a key role in tumor development, progression, and response to therapies. Elucidating the interplay between macrophages and NSCLC is crucial to fulfill the potential of macrophage-targeting strategies. We used NSCLC surgical specimens to generate multicellular spheroids enriched in cancer stem cells (CSCs) and highly responsive to microenvironmental cues. NSCLC spheroids were used to characterize state transitions induced by macrophage-tumor cell interactions in terms of proliferation, epithelial-to-mesenchymal transition (EMT), expression of stemness-related factors, self-renewal, and drug resistance. To define whether state transitions were induced by cell–cell contact or soluble factors, we compared direct co-cultures of spheroids and macrophages with transwell cultures, where cells are separated by a porous membrane. Cellular interactions were recorded by time-lapse microscopy and immunofluorescence (IF), whereas EMT, dormancy, stemness and chemoresistance were evaluated by real-time PCR, immunoblotting and functional assays. We found that co-cultures allowing cell–cell contact, but not transwell cultures, induced robust state transitions in NSCLC CSCs, promoting a state of dormancy associated with increased stemness, EMT and chemoresistance. In direct co-cultures (named NIDO, for Niche-Induced DOrmancy), macrophages and tumor cells formed nest-shaped aggregates and underwent a specular modulation of TGF-β levels, suggesting a physical transfer of this cytokine from macrophages to NSCLC cells within cellular nests. Treatment with Bafilomycin A1, an inhibitor of autophagosome-lysosome fusion and autolysosome acidification, inhibited TGF-β relocation and prevented the full spectrum of TGF-β-induced state transitions, including chemoresistance, EMT, and nest formation. By contrast, antibody-mediated TGF-β neutralization had only a partial effect, indicating secretory autophagy as a key mechanism underlying macrophage-tumor cell interplay. Altogether, these results show that lung macrophages crucially influence CSC phenotype, proliferation, and therapy resistance, pointing to a key role of local cell circuits in regulating tumor cell plasticity.</p><p></p>

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Tumor plasticity in macrophage niches promotes dormancy, EMT and chemoresistance of non-small cell lung cancer stem cells

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年7月31日

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  • Ann Zeuner,
  • Giovanni Sette,
  • Stefania Rossi,
  • Elena Landolfo,
  • Alessandro Vici,
  • Rachele Rossi,
  • Matilde Todaro,
  • Alice Turdo,
  • Vincenzo L. Lentini,
  • Michele Signore,
  • Alessandra Boe,
  • Eleonora Petrucci,
  • Maria Laura De Angelis,
  • Federica Francescangeli

摘要

Macrophages are the major immune cell type in the microenvironment of non-small cell lung cancer (NSCLC), playing a key role in tumor development, progression, and response to therapies. Elucidating the interplay between macrophages and NSCLC is crucial to fulfill the potential of macrophage-targeting strategies. We used NSCLC surgical specimens to generate multicellular spheroids enriched in cancer stem cells (CSCs) and highly responsive to microenvironmental cues. NSCLC spheroids were used to characterize state transitions induced by macrophage-tumor cell interactions in terms of proliferation, epithelial-to-mesenchymal transition (EMT), expression of stemness-related factors, self-renewal, and drug resistance. To define whether state transitions were induced by cell–cell contact or soluble factors, we compared direct co-cultures of spheroids and macrophages with transwell cultures, where cells are separated by a porous membrane. Cellular interactions were recorded by time-lapse microscopy and immunofluorescence (IF), whereas EMT, dormancy, stemness and chemoresistance were evaluated by real-time PCR, immunoblotting and functional assays. We found that co-cultures allowing cell–cell contact, but not transwell cultures, induced robust state transitions in NSCLC CSCs, promoting a state of dormancy associated with increased stemness, EMT and chemoresistance. In direct co-cultures (named NIDO, for Niche-Induced DOrmancy), macrophages and tumor cells formed nest-shaped aggregates and underwent a specular modulation of TGF-β levels, suggesting a physical transfer of this cytokine from macrophages to NSCLC cells within cellular nests. Treatment with Bafilomycin A1, an inhibitor of autophagosome-lysosome fusion and autolysosome acidification, inhibited TGF-β relocation and prevented the full spectrum of TGF-β-induced state transitions, including chemoresistance, EMT, and nest formation. By contrast, antibody-mediated TGF-β neutralization had only a partial effect, indicating secretory autophagy as a key mechanism underlying macrophage-tumor cell interplay. Altogether, these results show that lung macrophages crucially influence CSC phenotype, proliferation, and therapy resistance, pointing to a key role of local cell circuits in regulating tumor cell plasticity.