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Home Science News Cancer

Cholesterol-Lowering Drug Repurposed for HPV-Positive Cancer Treatment in Groundbreaking Clinical Trials at University Hospitals Seidman Cancer Center

February 28, 2025
in Cancer
Reading Time: 4 mins read
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Quintin Pan, PhD, Deputy Director of Research UH Seidman Cancer Center
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A groundbreaking study from the University Hospitals Seidman Cancer Center has paved the way for innovative clinical trials targeting HPV+ cancers with fenofibrate, a cholesterol-lowering medication. This effort marks a pivotal development in the treatment landscape for patients suffering from HPV+ cervical and head and neck cancers. The exploratory research, which shows remarkable promise, highlights fenofibrate’s ability to restore the functionality of crucial tumor suppressor genes.

The study’s preclinical results reveal that fenofibrate demonstrates efficacy comparable to that of cisplatin, a conventional chemotherapy agent, in combating HPV+ cancers. Researchers observed that this drug effectively mitigates the adverse effects of HPV-associated oncoproteins, specifically enhancing the function of the p53 tumor suppressor gene, often referred to as the "guardian of the genome." This gene plays a critical role in regulating the cell cycle and preventing tumor formation, making its restoration imperative for cancer therapy.

Wendi Quinn O’Neill, MS, DDS, a research scientist at the UH Seidman Cancer Center and the lead author of the study, expresses optimism about the implications of these findings. By comparing tissue samples from murine models treated with fenofibrate to untreated controls, her team documented a significant upregulation of p53 expression in the treated models. This revitalization of the gene suggests that fenofibrate not only interrupts tumor progression but reinvigorates the body’s intrinsic cancer-fighting mechanisms.

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The research team’s findings extend beyond merely restoring p53 function. O’Neill’s group observed that fenofibrate appears to initiate a reprogramming of the tumor microenvironment, an effect that could be advantageous in strategies for tumor eradication. In treated murine subjects, clusters of immune cells infiltrated the tumors, indicating an enhanced immune response. Some treated tumors exhibited signs of fibrous tissue and inflammatory cells, with notable instances showing no detectable tumors post-treatment.

For the first time, the anti-cancer potential of fenofibrate to reactivate p53 in HPV+ cancers is brought to light, representing a significant leap in research. The UH Seidman team is poised to validate their preclinical results through clinical trials. They will initiate two Phase 1 “window” trials, targeting patients diagnosed with HPV+ cervical cancer and HPV+ head and neck squamous cell carcinoma (HNSCC). These trials will administer fenofibrate during the interval between diagnosis and definitive surgical procedures, followed by detailed analyses of excised tissues.

As these trials commence, it is crucial to note that no therapeutic doses of fenofibrate will be evaluated initially. Instead, researchers aim to ascertain if the signaling pathway alterations observed in laboratory settings are consistent in clinical patients. Should these early results signify effectiveness, the subsequent steps could involve higher therapeutic doses.

The significance of this research rests on the understanding that HPV+ HNSCC requires distinct therapeutic approaches, as it is fundamentally different from cancers linked to traditional risk factors such as smoking and alcohol consumption. Current treatment protocols fail to differentiate these two categories, leading to a one-size-fits-all approach that may not maximize patient outcomes. O’Neill posits that by targeting the viral oncoproteins that drive HPV+ cancers, clinicians may administer more precise treatments that minimize toxicity and bolster therapeutic responses.

Furthermore, the potential of fenofibrate extends beyond treatment, as O’Neill notes its possible role in prevention. The integration of fenofibrate with existing therapies such as cisplatin or immunotherapies like anti-PD-1 checkpoint inhibitors might not only enhance their efficacy but also mitigate the side effects that often accompany conventional treatments. Given fenofibrate’s commendable safety profile, it presents an alluring option for long-term use in individuals susceptible to developing primary or recurrent HPV+ cancers.

These promising developments are undergirded by the support of the Kathy and Les Coleman Clinical Trials Center, which offers a plethora of clinical trials for cancer patients at the UH Seidman Cancer Center. For individuals seeking clinical trial opportunities, the center’s robust database provides access to innovative treatment modalities that may significantly alter the standard of care in oncology.

In summary, the exploration into fenofibrate’s applications in treating HPV+ cancers is at the cusp of transformative potential. As researchers strive to elucidate the mechanisms behind its cancer-fighting properties, the hope is that this cholesterol medication could redefine therapeutic strategies in oncology. The commitment to investigating clinically relevant dosages and treatment protocols may soon culminate in groundbreaking advancements that could greatly improve survival rates and quality of life for patients battling HPV-associated malignancies.

This forward-thinking research not only addresses a glaring gap in treatment strategies but also ushers in a new era of personalized medicine where therapies can be tailored to match the biological drivers of specific cancers. The implications of such work extend far beyond the confines of individual trials, with the potential to inspire future investigations into the repurposing of existing medications for cancer treatment.

As we anticipate the outcomes of the upcoming clinical trials, the scientific community and patients alike eagerly await the possibility that fenofibrate may emerge as a beacon of hope against the growing challenges posed by HPV+ cancers, ultimately transforming patient care and clinical outcomes in this field.

Subject of Research: The application of fenofibrate for treating HPV+ cervical and head and neck cancers.
Article Title: Fenofibrate: A New Hope in the Battle Against HPV-Linked Cancers.
News Publication Date: October 2023.
Web References: University Hospitals Seidman Cancer Center.
References: Cancers Journal.
Image Credits: University Hospitals Seidman Cancer Center.

Keywords: HPV+ cancers, fenofibrate, cervical cancer, head and neck cancer, clinical trials, p53 tumor suppressor, cholestrol-lowering drug, immunotherapy, targeted therapy, personalized medicine.

Tags: cancer treatment at University Hospitalscholesterol-lowering medication for cancer treatmentexploratory research in oncologyfenofibrate cancer trialsHPV-positive cervical cancer treatmentHPV+ head and neck cancer therapiesimplications of fenofibrate in oncologyinnovative cancer treatment strategiesp53 gene functionality in cancerpreclinical results in cancer drugsrepurposing medications for cancer therapytumor suppressor gene restoration
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