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P2X7 receptor: a critical regulator and potential target for breast cancer
Xiaodi Zhu1, Qianqian Li1, Wei Song1
1School of Medical Laboratory, Weifang Medical University, Weifang, Shandong, China.
Abstract:
Breast cancer is currently the most common cancer and the leading cause of cancer death among women worldwide. Advanced breast cancer is prone to metastasis, and there is currently no drug to cure metastatic breast cancer. The purinergic ligand-gated ion channel 7 receptor is an ATP-gated nonselective cation channel receptor and is involved in signal transduction, growth regulation, cytokine secretion, and tumor cell development. Recent studies have shown that upregulation of the P2X7 receptor in breast cancer can mediate AKT signaling pathways, Ca2 þ-activated SK3 potassium channels, and EMT and regulate the secretion of small extracellular vesicles to promote breast cancer invasion and migration, which are affected by factors such as hypoxia and ATP. In addition, studies have shown that microRNAs can bind to the 3' untranslated region of the P2X7 receptor, which affects the occurrence and development of breast cancer by upregulating and downregulating P2X7 receptor expression. Studies have shown that new P2X7 receptor inhibitors, such as emodin and Uncaria tomentosa, can inhibit P2X7 receptor-mediated breast cancer invasion and are expected to be used clinically. This article reviews the research progress on the relationship between the P2X7 receptor and breast cancer to provide new ideas and a basis for clinical diagnosis and treatment.
Insights
The P2X7 receptor (purinergic ligand-gated ion channel 7 receptor) promotes breast cancer metastasis. Inhibitors of this receptor show promise for treating advanced breast cancer, offering new clinical possibilities.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Breast cancer is a leading cause of cancer death globally, with advanced stages often metastasizing.
- Metastatic breast cancer lacks curative treatments.
- The P2X7 receptor (purinergic ligand-gated ion channel 7 receptor) is implicated in cellular processes relevant to cancer development.
Purpose of the Study:
- To review current research on the P2X7 receptor's role in breast cancer.
- To explore the mechanisms by which P2X7 receptor influences breast cancer progression.
- To highlight potential therapeutic strategies targeting the P2X7 receptor.
Main Methods:
- Literature review of studies investigating the P2X7 receptor in breast cancer.
- Analysis of molecular pathways and cellular processes affected by P2X7 receptor.
- Examination of preclinical data on P2X7 receptor inhibitors.
Main Results:
- P2X7 receptor upregulation in breast cancer promotes invasion and migration via AKT signaling, SK3 channels, EMT, and extracellular vesicle secretion.
- Hypoxia and ATP levels influence P2X7 receptor activity.
- MicroRNAs modulate P2X7 receptor expression, impacting breast cancer.
- Natural compounds like emodin and Uncaria tomentosa inhibit P2X7 receptor-mediated invasion.
Conclusions:
- The P2X7 receptor is a key mediator of breast cancer metastasis.
- Targeting the P2X7 receptor with inhibitors presents a promising therapeutic avenue for advanced breast cancer.
- Further research is needed to translate these findings into clinical applications for breast cancer treatment.
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