Emerging evidence suggests that local tumor radiotherapy reshapes the repertoire of circulating myeloid-derived suppressor cells (MDSCs) and leads to their infiltration into the tumor microenvironment, which poses a major obstacle for radiotherapy efficacy. Recent findings have identified RNA mA modification at the nexus of both anti-tumor immunity and radiation response. Here, we examine the mechanisms by which this RNA modification modulates the immune milieu of the radiation-remodeled tumor microenvironment. We discuss potential therapeutic interventions targeting mA machinery to improve radiotherapy response.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10751059 | PMC |
http://dx.doi.org/10.1016/j.medj.2023.09.001 | DOI Listing |
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