How mutations to a key liver cancer pathway contribute to tumour progression

Publicly released:
Australia; International; VIC

New Peter Mac research has found that mutations in one of the top 10 driver pathways in cancer - called the KEAP1-NRF2 pathway - increases the number of lysosomes in the cell. In healthy settings, lysosomes provide an important function to break down and dispose of damaged materials. However, in a cancer setting, lysosomes have been found to contribute to tumour progression. The research was led by Dr Andrew Cox and Dr Kristin Brown, who were motivated to understand how the KEAP1-NRF2 pathway contributes to the initiation of liver cancer.

Media release

From: Peter MacCallum Cancer Centre

Peter Mac scientists discover fundamental breakthrough in liver cancer development

New Peter Mac research recently published in Proceedings of the National Academy of Sciences (PNAS) has discovered a fundamental breakthrough related to the development of liver cancer.

The research team, led by Dr Andrew Cox and Dr Kristin Brown, were motivated to understand how the KEAP1-NRF2 pathway - identified as one of the top 10 driver pathways in cancer - contributes to the initiation of liver cancer.

They found that mutations in the KEAP1-NRF2 pathway rewire metabolism by increasing the number of lysosomes in the cell. In healthy settings, lysosomes provide an important function to break down and dispose of damaged materials in the cell. However, in a cancer setting, lysosomes have been found to contribute to tumour progression.

“It was through a combination of unbiased approaches that we came across the relationship between the KEAP1-NRF2 pathway and lysosomes,” Dr Brown said.

“We know that lysosomes make cancer cells grow even more out of control than they normally would and that they contribute to the development of therapy resistance.

“We're very excited about this research. We think there is huge potential with respect to understanding why liver cancer develops and how we can better treat patients diagnosed with this disease.

“It is incredibly important that we find out how lysosomes are regulated so that we can develop new cancer therapies in the future.”

With the incidence of liver cancer increasing and few existing therapeutic options to treat this disease, Dr Cox added that it’s therefore critical to understand the processes driving liver cancer development

“The KEAP1-NRF2 pathway plays an important role in protecting healthy liver cells from oxidative stress,” he said.

“Curiously, this pathway is mutated in a variety of cancers, including liver cancer. Our discovery that KEAP1-NRF2 pathway activation increases the abundance of lysosomes provides important fundamental insights into liver cancer development.”

This important collaborative work was carried out in the Cox and Brown labs and driven by PhD student Athena Ong, who is now working as a postdoctoral researcher at Peter Mac.

“Athena has already initiated follow-up studies to look more in depth at the role of the lysosome in liver cancer,” Dr Brown said.

This research was conducted with the support of the Peter Mac Foundation (Ted and Lila Seehusen Foundation). You can read the paper in full via the PNAS website here.

Journal/
conference:
PNAS
Research:Paper
Organisation/s: Peter MacCallum Cancer Centre, The University of Melbourne
Funder: A.J.S.O. and T.A.T. are supported by Australian Government Research Training Program Scholarships. K.J.E. is funded by NIH/ NCI (R01CA222570) and the Damon Runyon Cancer Research Foundation (Damon Runyon-Rachleff Innovation Award DRR-61-20). A.G.C. is supported by a National Health and Medical Research Council (NHMRC) Investigator Grant (GNT1176650), and an Australian Research Council Discovery Project Grant (DP200102693). K.K.B. is supported by NHMRC Ideas Grants (GNT2004212 and GNT2012313) and a Victorian Cancer Agency Mid-Career Research Fellowship (MCRF17020). K.K.B and A.G.C. are also jointly supported by the Peter MacCallum Cancer Foundation (Ted and Lila Seehusen Foundation).
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