Role of Tumor-Associated Macrophages in Sarcomas.
Tomohiro FujiwaraJohn HealeyKoichi OguraHiroya KondoHiroya KondoToshiaki HataHiroshi TazawaHiroshi TazawaToshiyuki KunisadaToshiyoshi FujiwaraToshiyoshi FujiwaraToshifumi OzakiPublished in: Cancers (2021)
Sarcomas are complex tissues in which sarcoma cells maintain intricate interactions with their tumor microenvironment. Tumor-associated macrophages (TAMs) are a major component of tumor-infiltrating immune cells in the tumor microenvironment and have a dominant role as orchestrators of tumor-related inflammation. TAMs promote tumor growth and metastasis, stimulate angiogenesis, mediate immune suppression, and limit the antitumor activity of conventional chemotherapy and radiotherapy. Evidence suggests that the increased infiltration of TAMs and elevated expression of macrophage-related genes are associated with poor prognoses in most solid tumors, whereas evidence of this in sarcomas is limited. Based on these findings, TAM-targeted therapeutic strategies, such as inhibition of CSF-1/CSF-1R, CCL2/CCR2, and CD47/SIRPα, have been developed and are currently being evaluated in clinical trials. While most of the therapeutic challenges that target sarcoma cells have been unsuccessful and the prognosis of sarcomas has plateaued since the 1990s, several clinical trials of these strategies have yielded promising results and warrant further investigation to determine their translational benefit in sarcoma patients. This review summarizes the roles of TAMs in sarcomas and provides a rationale and update of TAM-targeted therapy as a novel treatment approach for sarcomas.
Keyphrases
- high grade
- clinical trial
- induced apoptosis
- end stage renal disease
- cell cycle arrest
- early stage
- peritoneal dialysis
- ejection fraction
- chronic kidney disease
- prognostic factors
- radiation therapy
- gene expression
- locally advanced
- randomized controlled trial
- immune response
- drug delivery
- open label
- regulatory t cells
- phase ii
- cell proliferation
- rectal cancer
- double blind
- binding protein
- drug induced
- liver fibrosis