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Mice Survive Brain Cancer Tumors Lacking Key Surface Proteins

CWRU School of Medicine

Marc Kaplan
Associate Dean, Marketing and Communications
Case Western Reserve University School of Medicine

Case Western Reserve University researchers uncover proteins central for immune system avoidance

CLEVELAND – July 22, 2016 – A new scientific study has characterized a checkpoint protein that allows certain brain tumor cells to avoid the immune system. Tumors regularly avoid detection by decorating themselves with proteins that mimic those found on healthy cells. This protective shield allows them to grow undetected, often with deadly results. Brain tumors contribute to approximately 17,000 deaths annually with over 4,600 children newly diagnosed each year, according to the American Brain Tumor Association.

Tumors regulate their defensive shields by coordinating cascades of protein signals. These signals are often under the control of central coordinator proteins called serine/threonine kinases.

In the study published in the July 2016 edition of Science, researchers studied a protein called cyclin-dependent kinase 5 (Cdk5), a serine/threonine kinase that is essential for nerve and tumor cell development. The researchers specifically explored the role of Cdk5 in the development of medulloblastoma, a common, fast-growing pediatric brain tumor.

The researchers investigated Cdk5 because it is “commonly expressed in abundance and high Cdk5 levels correlate with a worse clinical prognosis in patients with melanoma, brain, breast, and lung cancers,” explained Alex Huang, MD, PhD, associate professor of pediatrics, pathology, and biomedical engineering at the School of Medicine, and co-senior author of the study. Agnes Petrosiute, MD, assistant professor of pediatrics at the School of Medicine, was the other senior author. Both are also pediatric oncologists at the Angie Fowler Adolescent & Young Adult Cancer Institute at University Hospitals Rainbow Babies & Children’s Hospital. Alex Huang, MD, PhD - Lab

When the researchers blocked Cdk5 inside tumor cells and injected them into mice, more than half of the mice survived. Nearly all of the mice injected with tumor cells still containing Cdk5 died. This suggested to the researchers that Cdk5 plays a central role in regulating the mice immune system response to tumors. By systematically depleting subsets of white blood cells in the mice, the researchers were able to identify CD4+ T cells as the primary immune cells responsible for removing the Cdk5-deficient tumor cells and sparing the mice from tumors.

Human T cells with CD4+ molecules on their surfaces communicate in part via an immune system signaling molecule called interferon-γ. Many tumor cells disrupt this communication mechanism by expressing a molecule on their own surfaces called programmed cell death-ligand 1 (PD-L1). The PD-L1 protein is also found on immune cells and normally helps “turn down” the immune system to avoid collateral damage once an immune response is complete. Tumor cells with PD-L1 on their surfaces can similarly deactivate T cells in their microenvironment and evade the immune system.

The researchers discovered that PD-L1 expression on tumor cells correlated with Cdk5 expression. They tested several types of tumor cells without Cdk5 and found them unable to robustly produce PD-L1 on their surfaces in response to immune signaling molecules. Without Cdk5 or PD-L1, the tumor cells were much more vulnerable to the immune system. The researchers confirmed this by disrupting the PD-L1 gene in tumor cells directly. Tumor cells without PD-L1 were unable to develop into lethal tumors in the majority of mice. These findings clearly show a central role for Cdk5 in modulating a tumor’s ability to produce PD-L1.

“We discovered that Cdk5, a protein commonly expressed in abundance, controls how tumors produce an essential checkpoint molecule, PD-L1,” said Huang. “Our discovery opens the door for molecular therapies targeting Cdk5 and associated signaling pathways as an alternative to current therapies that often have severe side effects.”

The central role for Cdk5 in driving PD-L1 expression appears to be highly specific. Other proteins that act in response to immune signaling molecules were not affected by the lack of Cdk5 in tumor cells.
Immune signaling molecules have many functions beyond triggering Cdk5 (and ultimately PD-L1) expression on tumor cells. The researchers used several techniques to tease apart the cascade of signals that connects immune signaling molecules to the tumor proteins. They identified 22 proteins that were differentially affected by the loss of Cdk5 in tumor cells, with a protein called IRF2BP2 most impacted. These proteins could potentially serve as therapeutic targets for anti-tumor medications in the future.

Approximately one-third of tumors can be combated by blocking PD-L1. This study shows that blocking Cdk5 may be another way to block PD-L1 on the surfaces of tumors and recruit CD4+ immune cells to shrink tumors. The researchers have characterized this pathway in medulloblastoma tumors, but preliminary evidence suggests it may also be applicable for other types of cancers.

Medulloblastoma accounts for approximately one-fifth of all pediatric brain tumors, according to the American Brain Tumor Association. The vast majority of diagnoses occur in children under age 10 and surgery is the primary treatment mechanism.

This work was supported by several National Institutes of Health (NIH) grants including NIH F31CA196265 (R.D.D.), NIH T32GM007250 (R.D.D. and S.M.C.), NIH T32AI089474 (S.M.C.), NIH R01GM086550 (D.W.A.), NIH R01CA154656 (A.Y.H.), NIH R21CA181875 (A.Y.H. and J.J.L.), NIH R01HL111682 (A.Y.H. and J.J.L.), and NIH P30CA043703 (A.Y.H. and A.P.), with additional funding from the Wolstein Research Scholarship (R.D.D.), St. Baldrick’s Foundation (A.P., J.J.L. and A.Y.H.), Hyundai “Hope-on-Wheels” Program (A.P., D.S.S. and A.Y.H.), Marc Joseph Fund (A.Y.H.), Alex’s Lemonade Stand Foundation (A.P. and A.Y.H.), the Angie Fowler AYA Cancer Research Initiative at the Case Comprehensive Cancer Center (A.P. J.J.L, D.S., S.A. and A.Y.H), Theresia G. & Stuart F. Kline Family Foundation in Pediatric Oncology (A.Y.H.), the Clinical and Translational Science Collaborative of Cleveland UL1TR000439 (A.P), and KL2TR000440 (S.A.) from the National Center for Advancing Translational Sciences (NCATS) component of the NIH.

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