Circumventing renal toxicity associated with cisplatin treatment: Study
Tokyo, Japan: Cisplatin is commonly used as a chemotherapeutic drug in the treatment of many solid tumours, including bladder, ovarian, and esophageal tumours. However, when it is metabolised by an enzyme called "cysteine conjugate beta-lyase 1 (CCBL1)," it is transformed to "thiol-cisplatin," a highly active poisonous metabolite. Though cisplatin treatment is accompanied with numerous adverse effects, this metabolite is known to induce kidney damage and is thus a key dose-limiting side effect of cisplatin treatment.
This research was headed by Associate Professor Hidetsugu Fujigaki of Fujita Health University and will be published in the journal Molecular Cancer Therapeutics on May 10, 2023.
As a treatment, vigorous or intravenous short-term injection of saline and mannitol is regarded standard of care. However, in many situations, these hydration regimes need hospitalisation. To enhance patient care, a group of Japanese researchers discovered that inhibiting the CCBL1-mediated metabolism of cisplatin with the aromatic ketone 2',4',6'-trihydroxyacetophenone (THA) can minimise cisplatin toxicity without compromising the drug's effectiveness]
Speaking about the study, Associate Professor Hidetsugu Fujigaki and a co-author, Nao Sukeda, a Master's student from Fujita Health University's Graduate School of Health Sciences say, "Using a high-throughput screening assay, we identified THA as an inhibitor of CCBL1. THA inhibited human CCBL1 b-elimination activity in a concentration-dependent manner."
To this end, the researchers first screened compound libraries for possible inhibitors of CCBL1, the enzyme responsible for the synthesis of cisplatin's toxic metabolite. This screening yielded THA, a naturally occurring compound from the Curcuma comosa rhizome, a plant of the ginger family, as an inhibitor of CCBL1 aminotransferase activity. They found THA to be an inhibitor of CCBL1 activity when testing with recombinant human CCBL1.
Investigating further, the researchers examined the protective in vitro and in vivo effects of THA on cisplatin-induced kidney damage using a variety of experimental techniques. For instance, they demonstrated that THA decreased the toxicity of cisplatin in healthy kidney cells derived from pigs that produced human CCBL1. Moreover, the researchers also observed that THA did not interfere with cisplatin's ability to reduce the proliferation of human- and murine- derived cancerous cells.
Explaining further, Professor Kuniaki Saito from Fujita Health University's Graduate School of Health Sciences says, "Upon examining the preventive effect of THA on cisplatin-induced nephrotoxicity, we noticed that THA attenuated the effect of cisplatin on the viability of confluent renal tubular cells but did not interfere with cisplatin-induced reduction in the proliferation of tumor cell lines including murine lung cancer and human breast cancer cells."
Next, the researchers observed that mice pre-treated with THA showed a significant reduction in cisplatin-induced pathological increases in blood urea nitrogen, creatinine, cell damage score, and kidney cell damage. Importantly, this THA pre-treatment also did not interfere with or adversely affect the anti-tumor efficacy of cisplatin in tumor-bearing mice.
"These effects might be attributed to the inhibition of the CCBL1-mediated formation of thiol-cisplatin. Our results suggest that THA might prevent cisplatin-induced nephrotoxicity and potentially provide a new strategy for patients receiving cisplatin-based cancer treatments," explains Associate Professor Fujigaki.
