Related Experiment Video
Updated: Jul 8, 2025

Evaluation of the Interplay Between the Complement Protein C1q and Hyaluronic Acid in Promoting Cell Adhesion
Published on: June 15, 2019
The multiple roles of C-type lectin receptors in cancer
1Tongji Hospital, Tongji Medical College, Huazhong University of Sciences and Technology, Wuhan, Hubei, China.
Abstract:
C-type lectin receptors are a family of immune response receptors that can bind with a broad repertoire of ligands. It can function as innative immune receptors to surveillance bacteria, fungi, and virus invasions. The expressions of C-type lectin receptors (CLRs) are found in different types of tumors. But the role of C-type lectin receptors in cancer is not fully elucidated. And the underlying mechanisms of CLRs in carcinogenesis and tumor development remained unknown. It is known that CLRs bind to the glycosylated antigen on the cancer cells, regulating cancer cell invasion, migration, and metastasis. Meanwhile, the recognition of tumor glycans by antigen-presenting cells can stimulate antitumor immune response and induce immune tolerance. Also, some types of CLRs can be used as diagnostic markers for tumor cells, suggesting that C-type lectin can function as a new tumor therapeutic target and potential biomarkers. Given the therapeutic potential of CLRs in tumor treatments and the emerging roles of CLR in the tumor hallmarks, the multiple roles of CLRs in cancer were summarized in this review.
Insights
C-type lectin receptors (CLRs) are immune receptors involved in cancer. This review summarizes their roles in tumor development, highlighting their potential as therapeutic targets and biomarkers.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- C-type lectin receptors (CLRs) are key innate immune receptors recognizing diverse ligands, including microbial components.
- CLRs are expressed in various tumor types, but their specific roles in cancer progression and the underlying mechanisms are not fully understood.
- Tumor-associated glycans are recognized by CLRs, influencing cancer cell behavior and immune responses.
Purpose of the Study:
- To review and summarize the multifaceted roles of C-type lectin receptors (CLRs) in cancer.
- To elucidate the mechanisms by which CLRs contribute to carcinogenesis and tumor development.
- To highlight the potential of CLRs as diagnostic markers and therapeutic targets in oncology.
Main Methods:
- Literature review synthesizing existing research on C-type lectin receptors in cancer.
- Analysis of studies investigating CLR expression patterns in different tumor types.
- Examination of the molecular mechanisms linking CLR-glycan interactions to cancer hallmarks like invasion, migration, and metastasis.
Main Results:
- C-type lectin receptors (CLRs) modulate cancer cell invasion, migration, and metastasis through binding to tumor-associated glycans.
- CLR recognition of tumor glycans by antigen-presenting cells can either stimulate anti-tumor immunity or induce immune tolerance.
- Certain CLRs show potential as diagnostic markers for tumor cells, indicating their utility in cancer diagnostics.
Conclusions:
- C-type lectin receptors (CLRs) play complex roles in cancer, influencing tumor progression and the anti-tumor immune response.
- The therapeutic potential of targeting CLRs for cancer treatment is significant, offering new avenues for drug development.
- CLRs represent promising biomarkers for cancer diagnosis and prognostication, warranting further investigation.
Related Concept Videos
Selectins
Cell Adhesion Molecules - Types and Functions
CAM Families
The Integrin family of proteins is primarily involved...
Immunoglobulin-like Cell Adhesion Molecules
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
Cadherins in Tissue Organization
Cell Sorting During Development
Cell sorting plays an...
Cancer Cell Migration through Invadopodia
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...

