Colorectal cancer (CRC) is a highly malignant disease that readily metastasises to vital organs.

Many strategies have been employed for clinical CRC therapy.

However, current treatments face significant limitations, such as drug toxicity, tumour recurrence, and drug resistance due to gene mutations in CRC cells.

Therefore, there is an urgent need to develop novel anti-tumour drugs that can effectively treat CRC patients with diverse genetic profiles.

This research, published in the Genes & Diseases journal by a team from the Sun Yat-sen University Cancer Centre, Sun Yat-sen Memorial Hospital, Affiliated Hospital of Jiangnan University, and Southern Medical University, focuses on a third-generation photosensitiser, Ce6-GFFY.

The researchers developed this novel molecule by covalently combining a photo-responsive Ce6 molecule with a GFFY peptide.

Ce6-GFFY forms stable macroparticles with an average size of 160 nm in solution, enabling targeted tumour penetration through the enhanced permeability and retention (EPR) effect.

In the in vitro studies, Ce6-GFFY demonstrated effective penetration and induced significant ROS production in CRC cells upon irradiation with a 660 nm laser.

Furthermore, results showed that CRT, a classical hallmark that acts as an “eat-me” signal, is highly expressed in Ce6-GFFY-treated CRC cells.

This suggests that Ce6-GFFY can effectively induce immunogenic cell death (ICD), indicating its promising potential for CRC therapy.

In the in vivo studies, the macroparticles exhibited a prolonged half-life in mice, demonstrating effective drug uptake and an extended therapeutic window.

The combined use of Ce6-GFFY and laser irradiation significantly activated anti-tumour immunity by promoting cytotoxic T cell infiltration while inhibiting the accumulation of myeloid-derived suppressor cells in tumours, thereby suppressing the growth of both primary and metastatic CRCs.

These findings suggest that Ce6-GFFY is a promising agent for CRC therapy with minimal side effects.

Unlike traditional treatments, photodynamic therapy (PDT) with Ce6-GFFY can destroy cancer cells regardless of genetic mutations, making it a versatile therapy option for patients who cannot be treated with any existing therapeutics, including those with clinical drug resistance.

In conclusion, the researchers highlight that the development of Ce6-GFFY represents a promising new strategy for the treatment of colorectal cancer.

Source: Compuscript Ltd