White matter neuroregeneration after chemotherapy: stem cell therapy for “chemobrain”
Grant Award Details
Grant Type:
Grant Number:
RN3-06510
Investigator(s):
Disease Focus:
Human Stem Cell Use:
Award Value:
$2,800,526
Status:
Closed
Progress Reports
Reporting Period:
Year 1
Reporting Period:
Year 2
Reporting Period:
Year 3
Reporting Period:
Year 5
Grant Application Details
Application Title:
White matter neuroregeneration after chemotherapy: stem cell therapy for “chemobrain”
Public Abstract:
Chemotherapy for cancer is often life saving, but it also causes a debilitating syndrome of impaired cognition characterized by deficits in attention, concentration, information processing speed, multitasking and memory. As a result, many cancer survivors find themselves unable to return to work or function in their lives as they had before their cancer therapy. These cognitive deficits, colloquially known as "chemobrain" or "chemofog," are long-lasting and sometimes irreversible. For example, breast cancer survivors treated with chemotherapy suffer from cognitive disability even 20 years later.
These cognitive problems occur because chemotherapy damages the neural stem and precursor cells necessary for the health of the brain's infrastructure, called white matter. We have discovered a powerful way to recruit the stem/precursor cells required for white matter repair that depends on an interaction between the electrical cells of the brain, neurons, and these white matter stem/precursor cells. In this project, we will determine the key molecules responsible for the regenerative influence of neurons on these white matter stem cells and will develop that molecule (or molecules) into a drug to treat chemotherapy-induced cognitive dysfunction. If successful, this will result in the first effective treatment for a disease that affects at least a million cancer survivors in California.
These cognitive problems occur because chemotherapy damages the neural stem and precursor cells necessary for the health of the brain's infrastructure, called white matter. We have discovered a powerful way to recruit the stem/precursor cells required for white matter repair that depends on an interaction between the electrical cells of the brain, neurons, and these white matter stem/precursor cells. In this project, we will determine the key molecules responsible for the regenerative influence of neurons on these white matter stem cells and will develop that molecule (or molecules) into a drug to treat chemotherapy-induced cognitive dysfunction. If successful, this will result in the first effective treatment for a disease that affects at least a million cancer survivors in California.
Statement of Benefit to California:
Approximately 100,000 Californians are diagnosed with cancer each year, and the majority of these people require chemotherapy. While cancer chemotherapy is often life saving, it also causes a debilitating neurocognitive syndrome characterized by impaired attention, concentration, information processing speed, multitasking and memory. As a result, many cancer survivors find themselves unable to return to work or function in their lives as they had before their cancer therapy. These cognitive deficits, colloquially known as "chemobrain" or "chemofog" are long-lasting; for example, cognitive deficits have been demonstrated in breast cancer survivors treated with chemotherapy even 20 years later. With increasing cancer survival rates, the number of people living with cognitive disability from chemotherapy is growing and includes well over a million Californians. Presently, there is no known therapy for chemotherapy-induced cognitive decline, and physicians can only offer symptomatic treatment with medications such as psychostimulants.
The underlying cause of "chemobrain" is damage to neural stem and precursor cell populations. The proposed project may result in an effective regenerative strategy to restore damaged neural precursor cell populations and ameliorate or cure the cognitive syndrome caused by chemotherapy. The benefit to California in terms of improved quality of life for cancer survivors and restored occupational productivity would be immeasurable.
Publications
- Dev Neurobiol (2018): Bad wrap: Myelin and myelin plasticity in health and disease. (PubMed: 28986960)
- Science (2017): Decoupling genetics, lineages, and microenvironment in IDH-mutant gliomas by single-cell RNA-seq. (PubMed: 28360267)
- Cell (2019): Methotrexate Chemotherapy Induces Persistent Tri-glial Dysregulation that Underlies Chemotherapy-Related Cognitive Impairment. (PubMed: 30528430)
- Cell (2017): Neural Precursor-Derived Pleiotrophin Mediates Subventricular Zone Invasion by Glioma. (PubMed: 28823557)
- Cell (2015): Neuronal Activity Promotes Glioma Growth through Neuroligin-3 Secretion. (PubMed: 25913192)
- Science (2014): Neuronal activity promotes oligodendrogenesis and adaptive myelination in the mammalian brain. (PubMed: 24727982)
- Nat Med (2018): Potent antitumor efficacy of anti-GD2 CAR T cells in H3-K27M(+) diffuse midline gliomas. (PubMed: 29662203)
- Nature (2017): Targeting neuronal activity-regulated neuroligin-3 dependency in high-grade glioma. (PubMed: 28959975)
- Cancer Cell (2017): Transcriptional Dependencies in Diffuse Intrinsic Pontine Glioma. (PubMed: 28434841)
- Neuron (2017): Wrapped to Adapt: Experience-Dependent Myelination. (PubMed: 28817797)