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The Role of ACKR3 in Breast, Lung, and Brain Cancer
Maria Neves1, Amos Fumagalli1, Jelle van den Bor1
1Departamento de Biología Molecular and Centro de Biología Molecular "Severo Ochoa" (UAM-CSIC), Universidad Autónoma Madrid, Madrid, Spain (M.N., F.M.); Institut de Génomique Fonctionnelle (IGF), Université de Montpellier, CNRS, INSERM, Montpellier, France (A.F., P.M.); Amsterdam Institute for Molecules, Medicines and Systems (AIMMS), Division of Medicinal Chemistry, Faculty of Science, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands (J.B., M.J.S.); and CIBER de Enfermedades Cardiovasculares (CIBERCV), Instituto de Salud Carlos III, Madrid, Spain (F.M.).
Abstract:
Recent reports regarding the significance of chemokine receptors in disease have put a spotlight on atypical chemokine receptor 3 (ACKR3). This atypical chemokine receptor is overexpressed in numerous cancer types and has been involved in the modulation of tumor cell proliferation and migration, tumor angiogenesis, or resistance to drugs, thus contributing to cancer progression and metastasis occurrence. Here, we focus on the clinical significance and potential mechanisms underlying the pathologic role of ACKR3 in breast, lung, and brain cancer and discuss its possible relevance as a prognostic factor and potential therapeutic target in these contexts.
Insights
Atypical chemokine receptor 3 (ACKR3) is overexpressed in many cancers, driving tumor progression and metastasis. Targeting ACKR3 may offer a new therapeutic strategy for breast, lung, and brain cancers.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- Chemokine receptors play a significant role in disease pathogenesis.
- Atypical chemokine receptor 3 (ACKR3) is increasingly recognized for its involvement in cancer.
Purpose of the Study:
- To investigate the clinical significance of ACKR3 in breast, lung, and brain cancers.
- To explore the mechanisms underlying ACKR3's role in cancer progression.
- To evaluate ACKR3 as a prognostic factor and therapeutic target.
Main Methods:
- Review of existing literature on ACKR3 in cancer.
- Analysis of ACKR3 expression patterns in various cancer types.
- Discussion of ACKR3's functional roles in tumor proliferation, migration, angiogenesis, and drug resistance.
Main Results:
- ACKR3 is overexpressed in multiple cancer types, including breast, lung, and brain cancer.
- ACKR3 contributes to cancer progression by modulating tumor cell proliferation, migration, angiogenesis, and drug resistance.
- ACKR3's overexpression correlates with cancer metastasis.
Conclusions:
- ACKR3 plays a critical pathologic role in breast, lung, and brain cancers.
- ACKR3 represents a potential prognostic biomarker and a promising therapeutic target for these cancers.
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