How targeted nutrients can fight cancer

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Australia; International; NSW
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An international research team has discovered a new way to effectively treat cancer, by using nutrients to reactivate suppressed metabolic pathways in cancer cells.

Media release

From: University of Technology Sydney (UTS)

An international research team has discovered a new way to effectively treat cancer, by using nutrients to reactivate suppressed metabolic pathways in cancer cells.

The researchers used a common amino acid, tyrosine, packaged as a nanomedicine, to change the metabolism of melanoma, a deadly skin cancer, and prevent cancer growth. 

Australia has the highest rate of skin cancer in the world. This new approach could be combined with current therapies to better treat melanoma. The technique also has the potential to treat other types of cancer.

The study, Nutrient-delivery and metabolism reactivation therapy for melanoma, was led by Professor Wenbo Bu from Fudan University and Distinguished Professor Dayong Jin from the University of Technology Sydney, and recently published in the prestigious journal Nature Nanotechnology.

Tyrosine has limited bioavailability in living organisms. However, the researchers used a new nanotechnology technique to package it into tiny particles called nanomicelles, which are attracted to cancer cell membranes, and break down easily, boosting absorption. 

The research team then tested the innovative treatment in mice and in human-derived melanoma cells in the lab and found that the tyrosine nanomicelles reactivated dormant metabolic pathways, triggered melanin synthesis, and inhibited tumour growth. 

“Uncontrolled rapid growth is a key feature that distinguishes cancer cells from normal cells. In cancer cells some metabolic pathways are over-activated, and others are suppressed, to create the environment necessary for rapid spread,” said Professor Jin.

“While a few metabolism-based drugs for cancer have been developed previously, such as aromatase inhibitors impeding estrogen synthesis in breast cancer and HK2 inhibitors targeting glycolysis in various cancers, these work by suppressing over-activate metabolic pathways,” he said.

“Our research shows for the first time that cancer can be stopped by reactivating metabolic pathways that are dormant. And this can be done using simple nutrients, such as amino acids, sugars, and vitamins, which are safe, readily available and well tolerated,” said Professor Bu.

Different types of cancer will respond to different nutrients. Melanoma cells develop from melanocytes – skin cells that produce melanin. Tyrosine is needed to produce melanin and it can stimulate melanin production, hence its effectiveness with melanoma. 

The reactivation of melanin synthesis forces the melanoma cell to reduce glycolysis, the process of converting sugar to energy, which is believed to be the mechanism for its anti-cancer effect.

Melanoma cells are also susceptible to heat stress. The researchers found that by combining tyrosine nanomicelle treatment with near-infrared laser treatment, they were able to eradicate melanoma in mice after six days and it did not reoccur during the study period.

The findings suggest a promising a new frontier in the use of nanomedicine for cancer therapy.

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Research Springer Nature, Web page
Media Release University of Technology Sydney (UTS), Web page
Journal/
conference:
Nature Nanotechnology
Research:Paper
Organisation/s: University of Technology Sydney (UTS), Fudan University
Funder: This work is supported by the Key Program of National Natural Science Foundation of China (22235004) and Innovation Program of Shanghai Municipal Education Commission (2023ZKZD01) to W.B.; National Natural Science Foundation of China (grant numbers 82172091 and 82372122) and Shanghai Science and Technology Innovation Action Plan (grant numbers 23XD1422800 and 23S31900200) to Y. Wu; and National Science Foundation for the Young Scientists of China (grant number 32000948) and State Key Laboratory of Molecular Engineering of Polymers Project (Fudan University, grant number K2023-24) to Y.C.
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