Myeloid-Derived Suppressor Cells and Macrophage Polarization in Cancer Immunotherapy DOI
Mohammad‐Salar Hosseini, Mohammad Amin Akbarzadeh, Farhad Jadidi‐Niaragh

et al.

Advances in medical diagnosis, treatment, and care (AMDTC) book series, Journal Year: 2024, Volume and Issue: unknown, P. 157 - 204

Published: Aug. 28, 2024

Myeloid-derived suppressor cells (MDSCs) and macrophage polarization are key functional components of the immune system in shaping tumor microenvironment (TME) modulating responses. MDSCs, characterized by their heterogeneity potent immunosuppressive functions, negatively affect anti-tumor immunity inhibiting T cell activation, promoting regulatory (Treg) expansion, enhancing growth metastasis. Similarly, into M1 (classically activated) M2 (alternatively phenotypes significantly influences progression, with macrophages facilitating immunosuppression, angiogenesis, tissue remodeling. Therapeutic strategies targeting these focus on depleting reprogramming from to phenotype, disrupting recruitment activation signals within TME. This chapter explores complex biology MDSCs polarized macrophages, interactions TME, impact cancer progression treatment outcomes, future landscape this field.

Language: Английский

The Multifaceted Role of Macrophages in Biology and Diseases DOI Open Access
Jan Brancewicz,

Natalia Wójcik,

Zuzanna Sarnowska

et al.

International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(5), P. 2107 - 2107

Published: Feb. 27, 2025

Macrophages are highly adaptable immune cells capable of responding dynamically to diverse environmental cues. They pivotal in maintaining homeostasis, orchestrating responses, facilitating tissue repair, and, under certain conditions, contributing disease pathogenesis. This review delves into the complex biology macrophages, highlighting their polarization states, roles autoimmune and inflammatory diseases, involvement cancer progression, potential as therapeutic targets. By understanding context-dependent functional plasticity we can better appreciate contributions health disease, paving way for innovative strategies.

Language: Английский

Citations

0

TPGS nanoparticles co-loaded with ABT-737 and R848 for breast cancer therapy DOI Creative Commons
Xiaoxue Lang, Xiangtao Wang, Meihua Han

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 177, P. 117107 - 117107

Published: July 11, 2024

Language: Английский

Citations

3

Decoding Cancer Evolution: Integrating Genetic and Non-Genetic Insights DOI Open Access
Arghavan Ashouri, Chufan Zhang, Federico Gaiti

et al.

Genes, Journal Year: 2023, Volume and Issue: 14(10), P. 1856 - 1856

Published: Sept. 24, 2023

The development of cancer begins with cells transitioning from their multicellular nature to a state akin unicellular organisms. This shift leads breakdown in the crucial regulators inherent multicellularity, resulting emergence diverse cell subpopulations that have enhanced adaptability. presence different within tumour, known as intratumoural heterogeneity (ITH), poses challenges for treatment. In this review, we delve into dynamics multicellularity unicellularity during onset and progression. We highlight role genetic non-genetic factors, well tumour microenvironment, promoting ITH evolution. Additionally, shed light on latest advancements omics technologies allow in-depth analysis tumours at single-cell level spatial organization tissue. Obtaining such detailed information is deepening our understanding evolutionary paths cancer, allowing effective therapies targeting key drivers

Language: Английский

Citations

7

m6A reader IGF2BP2 promotes M2 macrophage polarization and malignant biological behavior of bladder cancer by stabilizing NRP1 mRNA expression DOI Creative Commons
Dian Fu, Xiuquan Shi,

Xiaoming Yi

et al.

BMC Urology, Journal Year: 2024, Volume and Issue: 24(1)

Published: July 16, 2024

Abstract Background Insulin-like growth factor 2 mRNA-binding protein (IGF2BP2) has been confirmed to play oncogenic role in many cancers. However, the and mechanism of IGF2BP2 bladder cancer (BCa) still deserves be further revealed. Methods The mRNA levels neuronilin-1 (NRP1) were detected by real-time quantitative PCR (RT-qPCR) western blot. Cell proliferation, apoptosis, migration invasion determined using colony formation assay, EdU CCK8 flow cytometry transwell assay. Xenograft tumor model was conducted evaluate vivo. THP-1-M0 macrophages co-cultured with condition medium (CM) BCa cells induce polarization. M2 macrophage polarization assessed detecting markers RT-qPCR measuring proportion cytometry. Moreover, MeRIP RIP assay performed assess m6A level interaction between NRP1. Results NRP1 upregulated tissues cells. knockdown suppressed cell metastasis, as well inhibited growth. After CM cells, markedly enhanced, while this effect abolished knockdown. positively correlated level, it could increase stability. overexpression reversed suppressive on progression. Conclusion m6A-reader enhanced progression promoting

Language: Английский

Citations

2

Myeloid-Derived Suppressor Cells and Macrophage Polarization in Cancer Immunotherapy DOI
Mohammad‐Salar Hosseini, Mohammad Amin Akbarzadeh, Farhad Jadidi‐Niaragh

et al.

Advances in medical diagnosis, treatment, and care (AMDTC) book series, Journal Year: 2024, Volume and Issue: unknown, P. 157 - 204

Published: Aug. 28, 2024

Myeloid-derived suppressor cells (MDSCs) and macrophage polarization are key functional components of the immune system in shaping tumor microenvironment (TME) modulating responses. MDSCs, characterized by their heterogeneity potent immunosuppressive functions, negatively affect anti-tumor immunity inhibiting T cell activation, promoting regulatory (Treg) expansion, enhancing growth metastasis. Similarly, into M1 (classically activated) M2 (alternatively phenotypes significantly influences progression, with macrophages facilitating immunosuppression, angiogenesis, tissue remodeling. Therapeutic strategies targeting these focus on depleting reprogramming from to phenotype, disrupting recruitment activation signals within TME. This chapter explores complex biology MDSCs polarized macrophages, interactions TME, impact cancer progression treatment outcomes, future landscape this field.

Language: Английский

Citations

2