Involvement of Cellular Prion Protein in Invasion and Metastasis of Lung Cancer by Inducing Treg Cell Development
Autor: | Mi-Yeon Kim, Mi-Ji Sin, Mo-Jong Kim, Seunghwa Cha, Yong-Sun Kim, Hee-Jun Kim, Eun-Kyoung Choi |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Lung Neoplasms animal diseases Cell lcsh:QR1-502 Mice Transgenic Prnp0/0 Biology T-Lymphocytes Regulatory Biochemistry B7-H1 Antigen Article lcsh:Microbiology Metastasis prion Mice 03 medical and health sciences ME7 0302 clinical medicine Downregulation and upregulation Transforming Growth Factor beta medicine Animals Humans Cytotoxic T cell Neoplasm Invasiveness PrPC Proteins IL-2 receptor Neoplasm Metastasis Molecular Biology Cancer FOXP3 medicine.disease nervous system diseases Mice Inbred C57BL lung cancer 030104 developmental biology medicine.anatomical_structure 030220 oncology & carcinogenesis Cancer cell Cancer research Tga20 Treg cells |
Zdroj: | Biomolecules, Vol 11, Iss 285, p 285 (2021) Biomolecules Volume 11 Issue 2 |
ISSN: | 2218-273X |
DOI: | 10.3390/biom11020285 |
Popis: | The cellular prion protein (PrPC) is a cell surface glycoprotein expressed in many cell types that plays an important role in normal cellular processes. However, an increase in PrPC expression has been associated with a variety of human cancers, where it may be involved in resistance to the proliferation and metastasis of cancer cells. PrP-deficient (Prnp0/0) and PrP-overexpressing (Tga20) mice were studied to evaluate the role of PrPC in the invasion and metastasis of cancer. Tga20 mice, with increased PrPC, died more quickly from lung cancer than did the Prnp0/0 mice, and this effect was associated with increased transforming growth factor-beta (TGF-β) and programmed death ligand-1 (PD-L1), which are important for the development and function of regulatory T (Treg) cells. The number of FoxP3+CD25+ Treg cells was increased in Tga20 mice compared to Prnp0/0 mice, but there was no significant difference in either natural killer or cytotoxic T cell numbers. In addition, mice infected with the ME7 scrapie strain had decreased numbers of Treg cells and decreased expression of TGF-β and PD-L1. These results suggest that PrPC plays an important role in invasion and metastasis of cancer cells by inducing Treg cells through upregulation of TGF-β and PD-L1 expression. |
Databáze: | OpenAIRE |
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