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Novel cancer therapy extends lives of terminally ill dogs

Novel cancer therapy extends lives of terminally ill dogs
Cryopreservation and storage stability of MSC overexpressing CD::UPRT::GFP. (A) Cell images and transfection efficiency FACS profile of MSC overexpressing CD::UPRT::GFP before cryopreservation. Briefly, cells were plated and left overnight before addition of polyplex. 24 h post transfection, cells from multiple dishes were harvested and combined to obtain sufficient cells for storage and analysis. Flow cytometry (FACS) analysis was performed using CytoFLEX LX equipped with a FITC channel for GFP detection. Representative images are displayed. (B) Cell viability percentage was assessed using dye-exclusion assay (AO/DAPI, Chemometec) and transfection efficiency (flow cytometry analysis) for cryopreserved MSC overexpressing CD::UPRT::GFP at 5 months, 8 months and 11 months post cryopreservation. Significant differences in transfection efficiencies between modified MSCs before and post cryopreservation were calculated using two-tailed Student’s t test. **P < 0.005, ***P < 0.001. (C) MSC overexpressing CD::UPRT::GFP was stocked at 1 M, 20 M and 30 M/mL, and cell viability was measured 5 months post cryopreservation. (D) Post-thaw modified cells were spun down to remove CPA and resuspended in hypothermic storage solution HTS-FRS to assess stability at room temperature and 4 °C. Data of biological triplicates (n = 3) were expressed as mean ± SD. Credit: Stem Cell Research & Therapy (2022). DOI: 10.1186/s13287-022-03198-z

Dogs are humans' best friends and it is always distressing for dog owners when their beloved pets contract terminal illnesses. Canine cancer is the leading cause of death in dogs and when they are diagnosed with late-stage or terminal illness, there are often no treatment options available. In a recent study, however, a novel form of chemoimmunotherapy has proven to be a promising treatment in altering the course of the dogs' lives.

Scientists at the NUS Centre for Cancer Research (N2CR) Translational Research Programme (TRP) at the Yong Loo Lin School of Medicine, National University of Singapore (NUS Medicine) used stem cell precision engineering technology to treat the -stricken canines. In the study led by Associate Professor Too Heng-Phon from the N2CR TRP and Department of Biochemistry at NUS Medicine, the team modified Mesenchymal Stem Cells (MSCs), which are able to seek out cancerous tumors.

These modified cells carry a potent 'kill-switch' (cytosine deaminase) that produces a high, localized concentration of a cancer killing drug (5-fluorouracil) in the tumor environment and subsequently induces anti-cancer immunity. The development of this to treat canine patients leads the team toward a better understanding of cancer treatments, as well as its use in , as helping dogs with naturally occurring cancers provides valuable clues about .

Too said, "To repurpose stem cells for cancer treatment, it is usual to use viruses to introduce therapeutic genes into the cells. We have however, designed a non-viral gene delivery platform that introduces a high payload of therapeutic genes into the stem cells, to effectively destroy the out-of-control growing cancer cells. With this therapy that has been proven safe and demonstrated promising clinical benefits in animal patients, we hope to develop effective to help human patients with cancer as well, which can improve their health without compromising their quality of life."

Application of the technology on canine cancer patients

The technology developed by the NUS Medicine team was first applied on canine patients in Singapore in 2018, in a collaboration with Dr. Jean Paul Ly, Chief Executive Officer and Founder, Animal Wellness. The research team thereafter collaborated with more veterinary partners and institutions, delivered the therapy to a total of 65 dogs, as well as two cats, with conditions such as perianal adenoma, lung metastasis, and sarcoma.

The patients first received the precision-engineered MSCs through direct tumor-site injections or through blood stream, followed by the ingestion of oral pills containing a drug commonly used to treat fungal infection (5-flucytosine), over a few days. After a week, the cycle was repeated for two more weeks before the first course of treatment was completed. The team then monitored the condition of the patients and repeated the course where necessary.

Among the animal patients which received the treatment over a duration ranging from three to eight weeks, 56 showed signs of positive response, including 14 which showed full recovery from the treatment. Two animal patients remain cancer free, at least 30 months post treatment, while 46 patients showed good quality of life over two to 32 months, with the treatment. Through the course of treatment on all the animal patients involved in the study, there were no significant side effects observed—possibly due to the localized presence of the therapeutic cells which remain within the tumor environment.

Despite significant advancements in human cancer treatments, there is a massive lag in the development of oncology therapies for animal patients comparatively. Up until 2009, all animals were treated with generic human chemotherapy medicines on an off-label basis as there were no animal-specific anti-cancer agents approved by the U.S. Food and Drug Administration (FDA).

Dr. Lee Yee Lin, Founder and Head Veterinarian, Gentle Oak Veterinary Clinic in Singapore, who the research team collaborated with and is one of the authors of the study said, "Therapies and advances in allopathic medicine are usually developed primarily for humans, before they are applied to animals. As part of the trials for this study however, dogs with cancer with no other viable treatment options available are the primary receivers of the therapy—and many of them showed promising results with an improvement to their quality of life. Hopefully the therapy can become one of the standard options available to dogs in the near future, so that more patients can benefit from it."

One of the team's collaboration partners, Associate Professor Antonio Giuliano, Department of Veterinary Clinical Sciences, City University of Hong Kong, will also be taking the therapy into animal clinical studies in 2023.

Providing the therapy as an accessible and affordable option for human patients

The stem cell modification therapy differs from other cell and gene therapies that use viruses to introduce genes into cells. Instead of using virus, the modification involves using a chemical carrier, which is safer and faces less regulatory restrictions in the development of the treatment. Compared to other cell and gene therapies, the therapy design has a significantly shorter cycle and much lower costs of production, paving the way for a more accessible and affordable option for cancer patients in future.

Dr. Ho Yoon Khei, Senior Research Fellow, N2CR TRP and Department of Biochemistry at NUS Medicine, and first author and lead scientist of the study, said, "Currently, we can develop this therapy for up to 18 human patients every week. Beyond results that have shown to benefit our companion animals, it is our hope to extend the therapy to human patients in the future and improve healthcare outcomes for those who have cancer—especially when they have no treatment options left."

The research team is working with local and global health institutions to review the therapy's safety and efficacy for veterinary medicine and discuss plans for clinical trials on human patients in Singapore and the Asia Pacific region. These are expected to begin in 2024.

Prof Chong Yap Seng, Lien Ying Chow Professor in Medicine, Dean of NUS Medicine, added, "Our research work at NUS Medicine aims to create real, meaningful health benefits for the populations we serve, and eventually, drive better healthcare outcomes for all. We believe this therapy developed by the N2CR will have a major impact on the health and well-being of patients with solid tumors and late-stage cancer."

The work is published in the journal Stem Cell Research & Therapy.

More information: Yoon Khei Ho et al, Cryopreservation does not change the performance and characteristics of allogenic mesenchymal stem cells highly over-expressing a cytoplasmic therapeutic transgene for cancer treatment, Stem Cell Research & Therapy (2022). DOI: 10.1186/s13287-022-03198-z

Citation: Novel cancer therapy extends lives of terminally ill dogs (2023, January 30) retrieved 24 March 2023 from
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