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Understanding why deadly brain cancer comes back

Date:
August 22, 2022
Source:
University of Leeds
Summary:
Brain tumors may create interactions that hide them from the body's defenses. They can adapt to treatment by recruiting help from nearby healthy tissue. These interactions could be why these deadly cancers recur in almost all cases.
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The deadliest form of brain cancer returns because tumours adapt to treatment by recruiting help from nearby healthy tissue, say researchers who are trying to find a cure for the disease.

A new study, by a global team including University of Leeds experts, has found that in response to treatment, high-grade gliomas appear to remodel the surrounding brain environment, potentially creating interactions with nearby neurons and immune cells in ways that protect the tumour cells and hide them from the body's defences.

The team also found that lower grade tumours often develop a new mutation that allows the cells to start dividing more rapidly, potentially catapulting them into a higher-grade form.

Glioma brain tumours are rare, but a diagnosis is devastating because there is currently no cure. Low-grade gliomas have a better survival rate than, but often progress to high-grade gliomas. More than 90% of patients with high-grade tumours die within five years.

Current treatments include surgery, radiation therapy and chemotherapy. The findings indicate that new drugs are needed to supplement these.

Dr Lucy Stead, Associate Professor of Brain Cancer Biology in the University of Leeds' School of Medicine, and the lead UK academic for the study, said: "The brain is a hugely complex organ made up of lots of different types of cells, and brain tumours are equally diverse and complicated.

"Learning from patient tissue is the best way to cure the patient disease. This study, which required a global effort to acquire enough glioma samples to adequately power it, has allowed us to gain unprecedented insight into how these deadly tumours progress, and ways that we might finally be able to stop them."

Sue, a brain tumour patient from York, died in September 2017 after a seven-year battle with the disease. Her husband of 50 years, Geoff, is now an ambassador for Yorkshire's Brain Tumour Charity, taking part in events to help raise funds for brain cancer research and awareness.

Welcoming the findings, he said: "Sue fought bravely and without a single word of complaint or self-pity for 7 years. This is my driver. The types and positions of tumours make this a difficult one to actually "solve." But it is a scandal that the survival rate for brain tumours is no better now than 40 years ago.

"It seems from my experience that a one size fits all approach is applied to treatment at the moment and any form of targeting treatment specifically to suit the person must be an improvement.

"The fact that research is being undertaken has also a beneficial effect for patients and their families. It generates hope."

The researchers are investigating why gliomas progress to a higher-grade form, and why they survive and continue to grow after treatment.

They collected multiple samples of gliomas over time, as they transitioned from low-to-high grade, and before and after treatment. They then looked at how the cells changed and adapted to see if they can find ways to stop them, using novel drugs.

The mutation and previously unknown cellular interactions could now be targeted with novel drugs that stop the tumour cells progressing and adapting to treatment. In this way the study has opened new avenues of research that may yield more effective drugs to offer patients.

The research was led by Jackson Laboratory (JAX) Florine Deschenes Roux Chair Professor and senior author Dr Roel Verhaak and Postdoctoral Associate and Jane Coffins Childs fellow first author Dr Frederick Varn.

Dr Varn said: "By analyzing genetic and transcriptional data from this large cohort of patients, we are beginning to appreciate how tumors are changing to adapt to standard-of-care therapy.

"This study has made it clear that not every tumor changes in the same way. Knowing this is going to allow us to develop therapies that are better tailored towards each patient's disease in the future."

Dr Verhaak said: "The GLASS project has built tremendous momentum and is just getting started.

"We are well underway to tripling our patient cohort and datasets. We are poised to comprehensively dissect the process of resistance and make important progress towards better outcomes for patients with a glioma."

The University of Leeds' involvement in this international consortium is partly due to the presence of The Leeds Neuropathology Research Tissue Bank, which is co-funded by Yorkshire's Brain Tumour Charity and OSCAR's Paediatric Brain Tumour Charity

Marie Peacock, CEO at Yorkshire's Brain Tumour Charity, said: "We are delighted to be co-funding The Leeds Neuropathology Research Tissue Bank, ensuring that we have the research infrastructure needed to undertake research right here in Yorkshire to find new treatments and ultimately a cure for brain tumours."

Marie Hughes, who set up OSCARs Paediatric Brain Tumour Charity after her son died of a brain tumour in 2014, and whose husband and another son died from brain tumours in the past two years, said: "Supporting the work of The Tissue Bank is so important to us. Gliomas are the most common brain tumour in children and the research being conducted due to the presence in Leeds of this important research resource is essential in tailoring treatments to be less devastating and more efficient, and improving life outcomes.

"This is an extremely exciting project to be involved with as the impact that it will have on brain tumour research not just in Yorkshire but nationally and globally is enormous."


Story Source:

Materials provided by University of Leeds. Note: Content may be edited for style and length.


Journal Reference:

  1. Frederick S. Varn, Kevin C. Johnson, Jan Martinek, Jason T. Huse, MacLean P. Nasrallah, Pieter Wesseling, Lee A.D. Cooper, Tathiane M. Malta, Taylor E. Wade, Thais S. Sabedot, Daniel Brat, Peter V. Gould, Adelheid Wöehrer, Kenneth Aldape, Azzam Ismail, Santhosh K. Sivajothi, Floris P. Barthel, Hoon Kim, Emre Kocakavuk, Nazia Ahmed, Kieron White, Indrani Datta, Hyo-Eun Moon, Steven Pollock, Christine Goldfarb, Ga-Hyun Lee, Luciano Garofano, Kevin J. Anderson, Djamel Nehar-Belaid, Jill S. Barnholtz-Sloan, Spyridon Bakas, Annette T. Byrne, Fulvio D’Angelo, Hui K. Gan, Mustafa Khasraw, Simona Migliozzi, D. Ryan Ormond, Sun Ha Paek, Erwin G. Van Meir, Annemiek M.E. Walenkamp, Colin Watts, Tobias Weiss, Michael Weller, Karolina Palucka, Lucy F. Stead, Laila M. Poisson, Houtan Noushmehr, Antonio Iavarone, Roel G.W. Verhaak, Frederick S. Varn, Kevin C. Johnson, Jan Martinek, Jason T. Huse, MacLean P. Nasrallah, Pieter Wesseling, Lee A.D. Cooper, Tathiane M. Malta, Taylor E. Wade, Thais S. Sabedot, Daniel Brat, Peter V. Gould, Adelheid Wöehrer, Kenneth Aldape, Azzam Ismail, Santhosh K. Sivajothi, Floris P. Barthel, Hoon Kim, Emre Kocakavuk, Nazia Ahmed, Kieron White, Indrani Datta, Hyo-Eun Moon, Steven Pollock, Christine Goldfarb, Ga-Hyun Lee, Luciano Garofano, Kevin J. Anderson, Djamel Nehar-Belaid, Jill S. Barnholtz-Sloan, Spyridon Bakas, Annette T. Byrne, Fulvio D’Angelo, Hui K. Gan, Mustafa Khasraw, Simona Migliozzi, D. Ryan Ormond, Sun Ha Paek, Erwin G. Van Meir, Annemiek M.E. Walenkamp, Colin Watts, Tobias Weiss, Michael Weller, Kristin D. Alfaro, Samirkumar B. Amin, David M. Ashley, Christoph Bock, Andrew Brodbelt, Ketan R. Bulsara, Ana Valeria Castro, Jennifer M. Connelly, Joseph F. Costello, John F. de Groot, Gaetano Finocchiaro, Pim J. French, Anna Golebiewska, Ann C. Hau, Chibo Hong, Craig Horbinski, Kasthuri S. Kannan, Mathilde CM. Kouwenhoven, Anna Lasorella, Peter S. LaViolette, Keith L. Ligon, Allison K. Lowman, Shwetal Mehta, Hrvoje Miletic, Annette M. Molinaro, Ho Keung Ng, Simone P. Niclou, Johanna M. Niers, Joanna J. Phillips, Raul Rabadan, Ganesh Rao, Guido Reifenberger, Nader Sanai, Susan C. Short, Peter Sillevis Smitt, Andrew E. Sloan, Marion Smits, James M. Snyder, Hiromichi Suzuki, Ghazaleh Tabatabai, Georgette Tanner, William H. Tomaszewski, Michael Wells, Bart A. Westerman, Helen Wheeler, Jichun Xie, W.K. Alfred Yung, Gelareh Zadeh, Junfei Zhao, Karolina Palucka, Lucy F. Stead, Laila M. Poisson, Houtan Noushmehr, Antonio Iavarone, Roel GW. Verhaak. Glioma progression is shaped by genetic evolution and microenvironment interactions. Cell, 2022; 185 (12): 2184 DOI: 10.1016/j.cell.2022.04.038

Cite This Page:

University of Leeds. "Understanding why deadly brain cancer comes back." ScienceDaily. ScienceDaily, 22 August 2022. <www.sciencedaily.com/releases/2022/08/220822130441.htm>.
University of Leeds. (2022, August 22). Understanding why deadly brain cancer comes back. ScienceDaily. Retrieved March 28, 2024 from www.sciencedaily.com/releases/2022/08/220822130441.htm
University of Leeds. "Understanding why deadly brain cancer comes back." ScienceDaily. www.sciencedaily.com/releases/2022/08/220822130441.htm (accessed March 28, 2024).

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