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10.1002/dvdy.339

http://scihub22266oqcxt.onion/10.1002/dvdy.339
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33797140!?!33797140

suck abstract from ncbi

pmid33797140      Dev+Dyn 2022 ; 251 (1): 105-124
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  • Transforming growth factor-beta1 and myeloid-derived suppressor cells: A cancerous partnership #MMPMID33797140
  • Mojsilovic S; Mojsilovic SS; Bjelica S; Santibanez JF
  • Dev Dyn 2022[Jan]; 251 (1): 105-124 PMID33797140show ga
  • Transforming growth factor-beta1 (TGF-beta1) plays a crucial role in tumor progression. It can inhibit early cancer stages but promotes tumor growth and development at the late stages of tumorigenesis. TGF-beta1 has a potent immunosuppressive function within the tumor microenvironment that largely contributes to tumor cells' immune escape and reduction in cancer immunotherapy responses. Likewise, myeloid-derived suppressor cells (MDSCs) have been postulated as leading tumor promoters and a hallmark of cancer immune evasion mechanisms. This review attempts to analyze the prominent roles of both TGF-beta1 and MDSCs and their interplay in cancer immunity. Furthermore, therapies against either TGF-beta1 or MDSCs, and their potential synergistic combination with immunotherapies are discussed. Simultaneous TGF-beta1 and MDSCs inhibition suggest a potential improvement in immunotherapy or subverted tumor immune resistance.
  • |*Myeloid-Derived Suppressor Cells/pathology[MESH]
  • |*Neoplasms/pathology/therapy[MESH]
  • |Humans[MESH]
  • |Transforming Growth Factor beta1[MESH]
  • |Tumor Escape[MESH]


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