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The Role of Rarely Studied Chemokines in Tumor Progression in Multiple Myeloma (MM)
Jan Korbecki1, Mateusz Bosiacki2, Rafał Stelmach3
1Institute of Health Sciences, Collegium Medicum, University of Zielona Góra, 28 Zyty St., 65-046 Zielona Góra, Poland.
Abstract:
Multiple myeloma (MM) is a plasma cell neoplasm. Studies of chemokines in MM pathogenesis have primarily focused on CCR1 ligands such as CCL3 (MIP-1α), CXCL12 and its receptor CXCR4, as well as CXCR2 and CXCR3 ligands. However, the roles of the remaining 30 chemokines have been investigated much less frequently. This review compiles current knowledge on the significance of lesser-known chemokines in MM tumor processes, including CXCL13, CCR2 ligands (CCL2 [MCP-1], CCL7 [MCP-3]), CCL4, CCL5 (RANTES), CCL17, CCL20, CCL27, CCL28, and CX3CL1 (fractalkine). It describes their impact on bone destruction, bone marrow angiogenesis, chemoresistance, and the recruitment of cells into the MM niche, such as macrophages, myeloid-derived suppressor cells, and cytotoxic lymphocytes, along with their effects on mesenchymal stromal cells. A bioinformatic analysis highlights the significance of these chemokines in MM, and the possibility of targeting them in MM therapy is also considered.
Insights
This review explores understudied chemokines in multiple myeloma (MM), revealing their roles in tumor progression and potential as therapeutic targets for this plasma cell neoplasm.
Area of Science:
- Hematology
- Oncology
- Immunology
Background:
- Multiple myeloma (MM) is a plasma cell neoplasm.
- Research on chemokines in MM pathogenesis has mainly focused on specific ligands like CCL3, CXCL12, and their receptors.
- The roles of numerous other chemokines in MM remain underexplored.
Purpose of the Study:
- To review the significance of lesser-known chemokines in multiple myeloma.
- To elucidate their impact on tumor processes, including bone destruction, angiogenesis, and chemoresistance.
- To assess their influence on immune cell recruitment and mesenchymal stromal cells within the MM niche.
Main Methods:
- Literature review compiling current knowledge on lesser-known chemokines in MM.
- Description of the effects of specific chemokines (e.g., CXCL13, CCL2, CCL4, CCL5) on MM pathogenesis.
- Bioinformatic analysis to highlight the significance of these chemokines in MM.
Main Results:
- Lesser-known chemokines significantly influence MM tumor processes.
- These chemokines affect bone destruction, angiogenesis, and chemoresistance.
- They play crucial roles in recruiting various cells, including macrophages and lymphocytes, into the MM niche.
Conclusions:
- The review highlights the importance of understudied chemokines in multiple myeloma.
- These chemokines impact key MM pathologies and cellular interactions.
- Targeting these chemokines presents a potential therapeutic strategy for MM treatment.
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