Insights on CXC chemokine receptor 2 in breast cancer: An emerging target for oncotherapy
Fengzhu Guo1, Lang Long1, Jiantao Wang1
1Lung Cancer Center, Cancer Center, State Key Laboratory of Biotherapy, West China Hospital of Sichuan University, Chengdu, Sichuan 610041, P.R. China.
Abstract:
Breast cancer is the most common malignant neoplasm in women worldwide, and the treatment regimens currently available are far from optimal. Targeted therapy, based on molecular typing of breast cancer, is the most precise form of treatment, and CXC chemokine receptor 2 (CXCR2) is one of the molecular markers used in targeted therapies. As a member of the seven transmembrane G-protein-coupled receptor family, CXCR2 and its associated ligands have been increasingly implicated in tumor-associated processes. These processes include proliferation, angiogenesis, invasion, metastasis, chemoresistance, and stemness and phenotypic maintenance of cancer stem cells. Thus, the inhibition of CXCR2 or its downstream signaling pathways could significantly attenuate tumor progression. Therefore, studies on the biological functions of CXCR2 and its association with neoplasia may help improve the prognosis of breast cancer. Furthermore, the targeting of CXCR2 could supplement the present clinical approaches of breast cancer treatment strategies. The present review discusses the structures and mechanisms of CXCR2 and its ligands. Additionally, the contribution of CXCR2 to the development of breast cancer and its potential therapeutic benefits are also discussed.
Insights
Targeting CXC chemokine receptor 2 (CXCR2) shows promise for breast cancer treatment. Inhibiting CXCR2 may improve prognosis by impacting tumor progression, offering a new strategy beyond current therapies.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Breast cancer remains a leading cause of cancer-related deaths in women globally, with existing treatments often suboptimal.
- Molecular typing guides targeted therapy, and CXC chemokine receptor 2 (CXCR2) is identified as a key marker.
- CXCR2, a G-protein-coupled receptor, and its ligands are increasingly linked to various tumor-promoting processes.
Purpose of the Study:
- To review the biological functions and mechanisms of CXC chemokine receptor 2 (CXCR2) and its ligands.
- To elucidate the role of CXCR2 in breast cancer development and progression.
- To explore the potential of targeting CXCR2 as a therapeutic strategy for breast cancer.
Main Methods:
- Literature review focusing on structural and mechanistic aspects of CXCR2 and its ligands.
- Analysis of studies investigating the involvement of CXCR2 in breast cancer pathogenesis.
- Evaluation of preclinical and clinical data on CXCR2 inhibition in breast cancer models.
Main Results:
- CXCR2 signaling is implicated in critical tumor-associated processes including proliferation, angiogenesis, invasion, metastasis, and chemoresistance.
- CXCR2 plays a role in maintaining cancer stem cell populations and their stemness.
- Inhibition of CXCR2 or its downstream pathways demonstrates potential to impede tumor progression.
Conclusions:
- CXC chemokine receptor 2 (CXCR2) is a significant factor in breast cancer development and progression.
- Targeting CXCR2 presents a promising therapeutic avenue to improve breast cancer treatment outcomes.
- Further research into CXCR2 inhibition could supplement existing clinical strategies and enhance patient prognosis.
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