血小板
卵巢癌
癌症研究
癌细胞
血小板活化
免疫系统
癌症
化学
生物
细胞生物学
医学
免疫学
内科学
作者
Min Soon Cho,Hani Lee,Ricardo Gonzalez-Delgado,Dan Li,Tomoyuki Sasano,Wendolyn Carlos-Alcalde,Qing Ma,Jinsong Liu,Anil K. Sood,Vahid Afshar-Kharghan
出处
期刊:Cancers
[MDPI AG]
日期:2022-05-19
卷期号:14 (10): 2498-2498
被引量:13
标识
DOI:10.3390/cancers14102498
摘要
The interactions between platelets and cancer cells activate platelets and enhance tumor growth. Platelets increase proliferation and epithelial–mesenchymal transition in cancer cells, inhibit anoikis, enhance the extravasation of cancer cells, and protect circulating tumor cells against natural killer cells. Here, we have identified another mechanism by which platelets dampen the immune attack on cancer cells. We found that platelets can blunt the antitumor immune response by increasing the expression of inhibitory immune checkpoint (PD-L1) on ovarian cancer cells in vitro and in vivo. Platelets increased PD-L1 in cancer cells via contact-dependent (through NF-κB signaling) and contact-independent (through TFGβR1/Smad signaling) pathways. Inhibition of NF-κB or TGFβR1 signaling in ovarian cancer cells abrogated platelet-induced PD-L1 expression. Reducing platelet counts or inhibiting platelet functions reduced the expression of PD-L1 in ovarian cancer. On the other hand, an increase in platelet counts increased the expression of PD-L1 in tumor-bearing mice.
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