Blocking copper uptake in tumour cells may be clue to boosting immune system, fighting the deadliest of cancers

Blocking copper uptake in tumour cells may be clue to boosting immune system - fighting the deadliest of cancers
Dr Orazio Vittorio. Credit: University of New South Wales

Australian researchers have discovered that removing copper from the blood can destroy some of the deadliest cancers that are resistant to immunotherapy using models of the disease.

While immunotherapy, a treatment that works through a patient's immune system to kill the cancers, has proven to be a breakthrough for many , offering real hope and for some even a cure—some cancers camouflage themselves from current immunotherapies by expressing the aptly titled Programmed Death Ligand or PD-L1.

Dr. Orazio Vittorio and his team from Children's Cancer Institute in Sydney and UNSW Sydney published the findings today in Cancer Research, a journal of the American Association for Cancer Research.

It is known that such as brain "feed" on copper, often having up to six times the normal levels of the metal inside the tumor cells.

Dr. Vittorio and colleagues, including Professor Maria Kavallaris AM, studied tumor samples from more than 90 patients with neuroblastoma and 90 patients with gliomas. Both these cancers have and to date have not responded well to cancer immunotherapy.

Neuroblastoma accounts for 15% of total childhood cancer deaths and only 50% of patients with high-risk neuroblastoma patient survive their disease. Glioblastoma has the worst survival rate of all cancers, with only 5% of patients surviving 5 years past their diagnosis.

According to Dr. Vittorio, these two cancers express PD-L1 as a way to hide from the immune system, explaining why these two cancers are so deadly.

By looking at the human biopsies the researchers found a correlation between high levels of copper and increased expression of PD-L1. The researchers then showed for the first time that copper levels could control the expression of PD-L1 in cancer cells.

The researchers went on to use an analog of a drug, called TETA, that is currently used in the treatment of Wilson's Disease, which is a characterized by excess copper stored in various body tissues. They used this drug in animal models of neuroblastoma and glioblastoma to reduce the amount to in the tumor cells, leading to a reduction in the expression of PD-L1.

"When these mice were given immunotherapy there was a significant reduction in the size of their tumors," Dr. Vittorio said.

"Given that TETA is already in use in a number of clinical conditions and it is inexpensive and easy to manufacture, this may offer a viable treatment alternative for those cancers that are resistant to current immunotherapies."

Neuroblastoma claims more lives of children younger than five than any other cancer. Children like Luciano who was diagnosed at 14 months, endured three operations and eight rounds of chemotherapy. ''We are lucky because he responded well to treatment, but there were so many kids who have been lost. This research will help give hope to more families and children in the future'' his mother Maria said.

More information: Florida Voli et al. Intra-tumoral copper modulates PD-L1 expression and influences tumor immune evasion., Cancer Research (2020). DOI: 10.1158/0008-5472.CAN-20-0471

Journal information: Cancer Research
Citation: Blocking copper uptake in tumour cells may be clue to boosting immune system, fighting the deadliest of cancers (2020, August 19) retrieved 25 February 2024 from
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Drug used in breast and ovarian cancer could lead to safer, more effective treatment for neuroblastoma


Feedback to editors