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Discoidin Domain Receptor 2: A New Target in Cancer
Xiaoxiao Xu1, Tong Yu2, Zhenxing Wang3
1Department of Oncology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Background:
Discoidin domain receptor is a new and unique type of receptor tyrosine kinases, which binds to collagen, the main compose of an extracellular matrix. DDR1 was identified to mediate cell aggregation, and dysregulation of DDR2 has also been shown to be involved in tumor pathogenesis, although its role in cancer development and progression remains controversial.
Summary:
Abnormal expression and mutations of DDR2 have been reported in several cancer types and its participation in different aspects of tumor progression, including proliferation, migration, invasion, metastasis, epithelial-mesenchymal transition, and chemotherapy resistance. Moreover, novel DDR2 inhibitors have been designed and indicate a therapeutic effect for the cancer treatment.
Key Messages:
In this review, we summarize the current knowledge on the role of DDR2 in cancer promotion and the potential therapeutic value of targeting DDR2.
Insights
Discoidin domain receptor 2 (DDR2) plays a role in cancer progression, affecting proliferation, migration, and metastasis. Targeting DDR2 shows therapeutic potential for cancer treatment.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Discoidin domain receptor 2 (DDR2) is a receptor tyrosine kinase that interacts with extracellular matrix collagen.
- While DDR1 mediates cell aggregation, DDR2's specific role in cancer pathogenesis is debated.
Purpose of the Study:
- To review the current understanding of DDR2's function in promoting cancer.
- To explore the therapeutic potential of targeting DDR2 in cancer treatment.
Main Methods:
- Literature review of studies on DDR2 expression, mutations, and function in various cancers.
- Analysis of preclinical and clinical data on DDR2 inhibitors.
Main Results:
- Abnormal DDR2 expression and mutations are observed across multiple cancer types.
- DDR2 influences key cancer progression aspects: proliferation, migration, invasion, metastasis, epithelial-mesenchymal transition, and chemotherapy resistance.
Conclusions:
- DDR2 is implicated in various facets of tumor progression.
- Novel DDR2 inhibitors demonstrate therapeutic efficacy, highlighting DDR2 as a promising therapeutic target.
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