| Autor: |
Veena, Sangwan, Luai, Al-Marzouki, Sanjima, Pal, Vivian, Stavrakos, Malak, Alzahrani, Dorothy, Antonatos, Yehonatan, Nevo, Sophie, Camilleri-Broët, Roni, Rayes, France, Bourdeau, Betty, Giannias, Nicholas, Bertos, Swneke, Bailey, Simon, Rousseau, Jonathan, Cools-Lartigue, Jonathan D, Spicer, Lorenzo, Ferri |
| Rok vydání: |
2021 |
| Předmět: |
|
| Zdroj: |
Clinicalexperimental metastasis. 39(2) |
| ISSN: |
1573-7276 |
| Popis: |
Surgical resection, the cornerstone of curative intent treatment for gastric adenocarcinoma, is associated with a high rate of infection-related post-operative complications, leading to an increased incidence of metastasis to the peritoneum. However, the mechanisms underlying this process are poorly understood. Lipopolysaccharide (LPS), an antigen from Gram-negative bacteria, represents a potential mechanism via induction of local and systemic inflammation through activation of Toll-like receptor (TLR). Here, we use both a novel ex vivo model of peritoneal metastasis and in vivo animal models to assess gastric cancer cell adhesion to peritoneum both before and after inhibition of the TLR4 pathway. We demonstrate that activation of TLR4 by either LPS or Gram-negative bacteria (E. coli) significantly increases the adherence of gastric cancer cells to human peritoneal mesothelial cells, and that this increased adherence is abrogated by inhibition of the TLR4 signal cascade and downstream TAK1 and MEK1/2 pathways. We also demonstrate that the influence of LPS on adherence extends to peritoneal tissue and metastatic spread. Furthermore, we show that loss of TLR4 at the site of metastasis reduces tumor cell adhesion, implicating the TLR4 signaling cascade in potentiating metastatic adhesion and peritoneal spread. These results identify potential therapeutic targets for the clinical management of patients undergoing resection for gastric cancer. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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