Our Experiments show that serotonin – the neurotransmitter responsible for happiness – can stimulate cancer cells of the so-called Burkitt lymphoma to “commit suicide.”

Serotonin can penetrate the lymphoma cells and make them commit suicide (apoptosis = self-dissolution). Thus it carries the potential for effective therapy.

The body has 14 different serotonin receptors, and as we found out, the key to fighting tumors is in the transport protein.

For this study we used the novel SSRA 5-MMPA and the well-known SSRI Fluoxetine.

Although the experiments established the link between SSRAs and cancer, no epidemiological (statistical) evidence has yet been found.

Main findings

• SSRIs and SSRAs have shown an apoptotic effect, most likely by causing calcium to penetrate cells.
• Fluoxetine and 5-MMPA produce reactive oxygen species that initiate the destruction of the epidermal growth factor receptor.
• SSRIs interrupt the active signaling that leads to resistance to many chemotherapies.
• Fluoxetine has been shown to enhance the efficacy of temozolomide in several ways.
• Fluoxetine and 5-MMPA can cross the blood-brain barrier and are therefore ideal for glioblastomas.
• Fluoxetine inhibits multidrug-resistant efflux pumps and makes tumors more susceptible to standard chemotherapies such as doxorubicin, mytomycin C, and paclitaxel.
• Fluoxetine is the most effective chemosensitizer compared to other SSRIs approved for this purpose.
• SSRIs may reduce the efficacy of tamoxifen in estrogen receptor-positive breast cancer.

We will publish the entire study later this month.