New nanomedicines for a more efficient and less aggressive treatment of prostate cancer

(Nanowerk News) In Europe, prostate cancer is the most common type of cancer among men with an incidence greater than 100 cases per 100,000 individuals. Furthermore, it is currently the second most common cause of cancer-related deaths among men.
This pathology mainly affects elderly men: nine in 10 deaths take place after 65 years of age. Therefore, it represents a very serious health concern in developed countries, where the population of elderly men is majoritarian. In this context, even though docetaxel is the most used chemotherapy treatment for advanced prostate cancer, its high systemic toxicity limits both the dose as well as the duration of the therapy, which noticeably reduces its antitumour efficiency.
Now, a team of researchers from Valencia’s Polytechnic University (UPV), the Spanish National Research Council (CSIC), the La Fe University and Polytechnical Hospital and the Prince Philip Research Centre (CIPF), have developed a new nanomedicine to treat non-metastatic prostate cancer.
The tests conducted open the door for the future application of very effective treatments with very low doses of docetaxel.
“The antitumour activity of docetaxel was improved up to a hundredfold in the in vitro studies on prostate cancer cells with PSMA receptors,” highlights Pablo Botella, head scientist of the CSIC in the Chemical Technology Institute, mixed centre of the UPV and CSIC.
Following the in vitro study, the work is currently in a phase of in vivo pre-clinical tests. Meanwhile, clinical trials – phase I – should begin in under two years on a reduced number of patients.

Facilitating the diagnosis

Furthermore, researchers have also developed a new nanomarker which enables the identification of tumour tissue in the prostate with great accuracy. “Thanks to the PET image technique, we can flag the nanomedicine with a radioactive isotope which makes it possible to locate the malign tissue in the prostate with unicellular precision, which will facilitate the diagnosis of the disease in its initial stages, thus making its early detection easier,” adds Botella.
These results have been published in the journal ACS Omega("PSMA-Targeted mesoporous silica nanoparticles for selective intracellular delivery of docetaxel in prostate cancer cells").

What is the new nanomedicine like?

The new nanomedicine developed by these researchers is a system based on porous silica nanoparticles, functionalised with the docetaxel medicine and a monoclonal antibody (anti-FOLH1) which selectively interacts with the PSMA receptors of prostate cancer cells. The system shows great stability in biological fluids and all its components are approved by the Food and Drug Administration (FDA, United States) for clinical use.
The presence of the monoclonal antibody promotes the cellular internalisation of the nanomedicine into the malignant cells (at least 25% more compared to simply administering the medicine, as this spreads to any cell, whether cancerous or not). This way, the nanomedicine reaches more tumour cells. Furthermore, the use of a specific anchoring protocol of docetaxel to the nanoparticles enables its selective release inside the cancerous cells.

CURSOL foundation and TETRACAP project

This work was initially funded by the CURSOL (Valencian Community Resource and Solidarity Culture) foundation, and is currently integrated within the TETRACAP project, which is funded by the Valencian government, and whose principal researcher is professor Jose María Benlloch, head of the Molecular Image Instrumentation Institute (I3M), mixed centre of the UPV and CSIC.
In this project, together with the I3M, researchers of the Chemical Technology Institute also took part, headed by Dr. Pablo Botella. Furthermore, a team of the La Fe hospital also participated, headed by Dr. Cesar David Vera-Donoso; and another from the Prince Philip Research Centre, headed by Dr. Victoria Moreno. The in vivo and clinical trials are supervised in these centres.
Source: Asociación RUVID
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