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Updated: Feb 3, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
TRPV2 is a novel biomarker and therapeutic target in triple negative breast cancer
Mohamad Elbaz1,2,3, Dinesh Ahirwar1,2, Zhang Xiaoli4
1Department of Pathology, Wexner Medical Center, Ohio State University (OSU), Columbus, OH, USA.
Abstract:
Transient receptor potential vanilloid type-2 (TRPV2) is an ion channel that is triggered by agonists like cannabidiol (CBD). Triple negative breast cancer (TNBC) is an aggressive disease with limited therapeutic options. Chemotherapy is still the first line for the treatment of TNBC patients; however, TNBC usually gains rapid resistance and unresponsiveness to chemotherapeutic drugs. In this study, we found that TRPV2 protein is highly up-regulated in TNBC tissues compared to normal breast tissues. We also observed that TNBC and estrogen receptor alpha negative (ERβ-) patients with higher TRPV2 expression have significantly higher recurrence free survival compared to patients with lower TRPV2 expression especially those who were treated with chemotherapy. In addition, we showed that TRPV2 overexpression or activation by CBD significantly increased doxorubicin (DOX) uptake and apoptosis in TNBC cells. The induction of DOX uptake was abrogated by TRPV2 blocking or downregulation. In vivo mouse model studies showed that the TNBC tumors derived from CBD+DOX treated mice have significantly reduced weight and increased apoptosis compared to those treated with CBD or DOX alone. Overall, our studies for the first time revealed that TRPV2 might be a good prognostic marker for TNBC and ERβ- breast cancer patient especially for those who are treated with chemotherapy. In addition, TRPV2 activation could be a novel therapeutic strategy to enhance the uptake and efficacy of chemotherapy in TNBC patients.
Insights
Transient receptor potential vanilloid type-2 (TRPV2) shows higher expression in triple-negative breast cancer (TNBC). Activating TRPV2 with CBD enhances chemotherapy efficacy and improves survival for TNBC patients.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Triple-negative breast cancer (TNBC) is aggressive with limited treatment options.
- TNBC often develops resistance to chemotherapy.
- Transient receptor potential vanilloid type-2 (TRPV2) is an ion channel implicated in cellular processes.
Purpose of the Study:
- To investigate the role of TRPV2 in TNBC.
- To evaluate TRPV2 as a prognostic marker in breast cancer.
- To explore TRPV2 activation as a therapeutic strategy for TNBC.
Main Methods:
- Analysis of TRPV2 protein expression in TNBC tissues.
- Correlation of TRPV2 expression with patient survival and chemotherapy response.
- In vitro studies using TNBC cell lines to assess the effect of TRPV2 activation (CBD) on doxorubicin (DOX) uptake and apoptosis.
- In vivo studies using a mouse model of TNBC.
Main Results:
- TRPV2 is significantly upregulated in TNBC tissues compared to normal breast tissues.
- Higher TRPV2 expression correlates with improved recurrence-free survival in TNBC and ERβ- patients, particularly those receiving chemotherapy.
- TRPV2 activation by CBD enhanced doxorubicin uptake and apoptosis in TNBC cells, an effect blocked by TRPV2 inhibition.
- Combined CBD and doxorubicin treatment significantly reduced tumor weight and increased apoptosis in vivo.
Conclusions:
- TRPV2 may serve as a valuable prognostic marker for TNBC and ERβ- breast cancer patients undergoing chemotherapy.
- TRPV2 activation presents a potential novel therapeutic strategy to improve chemotherapy efficacy in TNBC.
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