Pharmacologic Hedgehog inhibition modulates the cytokine profile of osteolytic breast cancer cells

• Published in: Journal of bone oncology 2024-08, Vol.47, p.100625, Article 100625
• Main Authors: Bennett, Natalie E., Parker, Dominique V., Mangano, Rachel S., Baum, Jennifer E., Northcutt, Logan A., Miller, Jade S., Beadle, Erik P., Rhoades, Julie A.
• Format: Article
• Language: English
• Subjects: Bone metastasis; Breast cancer; Cytokine; Monocyte; Myeloid; M−CSF
• ISSN: 2212-1374; 2212-1374
• DOI: 10.1016/j.jbo.2024.100625

•Gli2 correlates with myeloid gene signatures in sequencing data of patient tumors.•HPI-1 treatment alters transcription and secretion of cytokines, including M−CSF.•This altered secretory profile induces a proinflammatory phenotype in monocytes. The establishment and progression of bone metastatic breast cancer is supported by immunosuppressive myeloid populations that enable tumor growth by dampening the innate and adaptive immune response. Much work remains to understand how to target these tumor-myeloid interactions to improve treatment outcomes. Noncanonical Hedgehog signaling is an essential component of bone metastatic tumor progression, and prior literature suggests a potential role for Hedgehog signaling and its downstream effector Gli2 in modulating immune responses. In this work, we sought to identify if inhibition of noncanonical Hedgehog signaling alters the cytokine profile of osteolytic breast cancer cells and the subsequent communication between the tumor cells and myeloid cells. Examination of large patient databases revealed significant relationships between Gli2 expression and expression of markers of myeloid maturation and activation as well as cytokine expression. We found that treatment with HPI-1 reduced tumor cell expression of numerous cytokine genes, including CSF1, CSF2, and CSF3, as well as CCL2 and IL6. Secreted CSF-1 (M−CSF) was also reduced by treatment. Changes in tumor-secreted factors resulted in polarization of THP-1 monocytes toward a proinflammatory phenotype, characterized by increased CD14 and CD40 surface marker expression. We therefore propose M−CSF as a novel target of Hedgehog inhibition with potential future applications in altering the immune microenvironment in addition to its known roles in reducing tumor-induced bone disease.