Chemotherapeutic Targeting of Myeloid-derived Suppressor Cells
Overview
Affiliations
Myeloid-derived suppressor cells (MDSCs), which expand in cancer-bearing hosts, contribute to the escape of malignant cells from immune destruction and impair the efficacy of immunotherapeutic interventions. We have recently demonstrated that the conventional chemotherapeutic agent doxorubicin selectively eliminates MDSCs, hence promoting the activity of immune effector cells and improving the therapeutic profile of adoptively transferred helper T lymphocytes.
Solimando A, Vacca A, Ribatti D J Oncol. 2020; 2020:6820241.
PMID: 32508920 PMC: 7251466. DOI: 10.1155/2020/6820241.
Geng F, Bao X, Dong L, Guo Q, Guo J, Xie Y Oncoimmunology. 2020; 9(1):1747350.
PMID: 32363118 PMC: 7185204. DOI: 10.1080/2162402X.2020.1747350.
Doxorubicin modulated clock genes and cytokines in macrophages extracted from tumor-bearing mice.
Teixeira A, Biondo L, Silveira L, Lima E, Batatinha H, Diniz T Cancer Biol Ther. 2020; 21(4):344-353.
PMID: 31931676 PMC: 7515505. DOI: 10.1080/15384047.2019.1702400.
Parihar R, Rivas C, Huynh M, Omer B, Lapteva N, Metelitsa L Cancer Immunol Res. 2019; 7(3):363-375.
PMID: 30651290 PMC: 7906796. DOI: 10.1158/2326-6066.CIR-18-0572.
Trial Watch: Proteasomal inhibitors for anticancer therapy.
Obrist F, Manic G, Kroemer G, Vitale I, Galluzzi L Mol Cell Oncol. 2016; 2(2):e974463.
PMID: 27308423 PMC: 4904962. DOI: 10.4161/23723556.2014.974463.