4.6 Review

Focusing on discoidin domain receptors in premalignant and malignant liver diseases

Journal

FRONTIERS IN ONCOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2023.1123638

Keywords

discoidin domain receptors; liver; cancer; extracellular matrix; metastasis; therapy

Categories

Ask authors/readers for more resources

DDRs are receptor tyrosine kinases that bind to extracellular collagens and are rarely expressed in normal liver tissues. Recent studies have shown that DDRs play a significant role in premalignant and malignant liver diseases. DDR1 promotes inflammation, fibrosis, invasion, migration, and liver metastasis of tumor cells, while DDR2 may have different roles in early-stage liver injury, chronic liver fibrosis, and metastatic liver cancer. This review provides a detailed description of these findings and aims to provide new insights for cancer treatment and translation from bench to bedside.
Discoidin domain receptors (DDRs) are receptor tyrosine kinases on the membrane surface that bind to extracellular collagens, but they are rarely expressed in normal liver tissues. Recent studies have demonstrated that DDRs participate in and influence the processes underlying premalignant and malignant liver diseases. A brief overview of the potential roles of DDR1 and DDR2 in premalignant and malignant liver diseases is presented. DDR1 has proinflammatory and profibrotic benefits and promotes the invasion, migration and liver metastasis of tumour cells. However, DDR2 may play a pathogenic role in early-stage liver injury (prefibrotic stage) and a different role in chronic liver fibrosis and in metastatic liver cancer. These views are critically significant and first described in detail in this review. The main purpose of this review was to describe how DDRs act in premalignant and malignant liver diseases and their potential mechanisms through an in-depth summary of preclinical in vitro and in vivo studies. Our work aims to provide new ideas for cancer treatment and accelerate translation from bench to bedside.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available