iNtRON Biotechnology, Inc. announced that iNtRON has demonstrated the effectiveness of P18-BE3CRC using a cancer organoid model. P18-BE3CRC is a drug candidate of PHAGERIA® platform technology, which is for the development and commercialization of bacteriophage-based drugs (Phageome API) effective for cancer control. According to the company's explanation, bacteriophages have been mainly used for R&D on bacterial infectious diseases, but recently the scope of application of bacteriophages has been expanded to the anti-cancer field by the company.

The company has begun to focus on related development and successfully secured a new platform technology called PHAGERIA®. The first target cancer type of PHAGERIA® technology is colorectal cancer (CRC). Chromosomal instability (CIN), microsatellite instability (MSI), and CpG island methylator phenotype (CIMP) are mainly described as molecular pathological features of CRC.

It is predicted that the essential cause would be not much different from the general causes of cancer, such as genetic factors including family history, aging, smoking, and westernized eating habits, but the actual cause has not yet been clarified. Recently, attention has been drawn to the possibility that a certain microbiome in the colon can be a major cause of colorectal cancer. Accordingly, there have been may researches regarding the microbiome and the pathogenesis of colorectal cancer along with the isolation and identification of the microbiome associated with colorectal cancer.

The reason for this interest is the expectation that effective control of the microbiome in the colon may not only prevent cancer, but also prevent relapse or metastasis after surgery. Among the various microbiomes, iNtRON Bio is paying attention to enterotoxigenic Bacteroides fragilis (ETBF) and pks+ E. coli, which secrete toxins such as BFT (Bacteroides fragilis toxin) and Colibactin, respectively. iNtRON Bio is working on related researches to develop 'First-in-Concept' drugs to control the harmful microbiome through the phageome.

According to recent reports, the above-mentioned two microbiomes are present in over 70% of colorectal cancer patients and about 60% in normal individuals, indicating that the microbiome is closely related to the onset and progression of colorectal cancer. To verify the cancer control effect of the PHAGERIA® candidate, a culture method for organoids derived from healthy human colon tissue was established, and induced tumorigenesis by treating them with ETBF and pks+ E. coli. As comparing the cases with or without administering PHAGERIA® candidate, it was confirmed that administering PHAGERIA® candidate significantly inhibited tumorigenesis.

Thus, if the microbiome that causes cancer can be maintained in a low level in the body, it may be possible to prevent the recurrence or metastasis of cancer, increasing the utility of PHAGERIA® (phageome) as a new cancer- controlling drugs.