Macrophages as a Potential Immunotherapeutic Target in Solid Cancers.
Alok K MishraShahid BandayRavi BharadwajAmjad AliRomana RashidAnkur KulshreshthaSunil K MaloniaPublished in: Vaccines (2022)
The revolution in cancer immunotherapy over the last few decades has resulted in a paradigm shift in the clinical care of cancer. Most of the cancer immunotherapeutic regimens approved so far have relied on modulating the adaptive immune system. In recent years, strategies and approaches targeting the components of innate immunity have become widely recognized for their efficacy in targeting solid cancers. Macrophages are effector cells of the innate immune system, which can play a crucial role in the generation of anti-tumor immunity through their ability to phagocytose cancer cells and present tumor antigens to the cells of adaptive immunity. However, the macrophages that are recruited to the tumor microenvironment predominantly play pro-tumorigenic roles. Several strategies targeting pro-tumorigenic functions and harnessing the anti-tumorigenic properties of macrophages have shown promising results in preclinical studies, and a few of them have also advanced to clinical trials. In this review, we present a comprehensive overview of the pathobiology of TAMs and their role in the progression of solid malignancies. We discuss various mechanisms through which TAMs promote tumor progression, such as inflammation, genomic instability, tumor growth, cancer stem cell formation, angiogenesis, EMT and metastasis, tissue remodeling, and immunosuppression, etc. In addition, we also discuss potential therapeutic strategies for targeting TAMs and explore how macrophages can be used as a tool for next-generation immunotherapy for the treatment of solid malignancies.
Keyphrases
- induced apoptosis
- cancer therapy
- clinical trial
- papillary thyroid
- immune response
- cell cycle arrest
- healthcare
- oxidative stress
- cancer stem cells
- dendritic cells
- squamous cell
- epithelial mesenchymal transition
- randomized controlled trial
- anti inflammatory
- endoplasmic reticulum stress
- squamous cell carcinoma
- human health
- climate change
- poor prognosis
- risk assessment
- long non coding rna
- regulatory t cells
- lymph node metastasis
- cell proliferation
- vascular endothelial growth factor
- chronic pain
- replacement therapy
- african american
- combination therapy
- type iii