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Developing trustworthy artificial intelligence for language-based assessment of neurodegenerative disorders: Enabling early detection of Cognitive decline with inexpensive, scalable technologies

ÌýÌýPeter S. Pressman (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Department of Neurology)
ÌýÌýPeter W. Foltz (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Institute for Cognitive Science)
ÌýÌýNew collaboration

This project seeks to improve the diagnosis of dementia through the development of sensitive and usable AI-based tools that analyze speech to enable earlier detection and thus more timely interventions than is in current practice.

Drug discovery targeting the PARP1–HPF1 complex for the treatment of cancer (co-sponsored by the University of Colorado Cancer Center)

ÌýÌýDan LaBarbera (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Department of Pharmaceutical Sciences)
ÌýÌýKarolin Luger (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Department of Biochemistry)
ÌýÌýNew collaboration

PARP inhibitors (e.g., Olaparib) have revolutionized the clinical treatment of cancer, particularly breast, ovarian, and pancreatic cancers. However, PARP inhibitors are plagued by significant drug resistance mechanisms. This proposal will execute a new drug discovery and therapeutic strategy to target a protein complex with PARP implicated in cancer.

Efflux pump inhibitors and mycobacterium tuberculosis (Mtb)

ÌýÌýMartin Voskuil (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Associate Professor of Immunology and Microbiology)
ÌýÌýCorrie Detweiler (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Professor of Molecular, Cellular and Developmental Biology)
ÌýÌýNew collaborationÌý($50,000)

Our new collaboration will determine whether compounds that inhibit bacterial export systems in human bacterial pathogens also have efficacy against the causative agent of human tuberculosis, Mycobacterium Tuberculosis. The research has the potential to suggest new treatments for tuberculosis.

Exploiting biomechanical properties of peripheral CD8+ T cells in adoptive cell therapies for cancer (co-sponsored by the University of Colorado Cancer Center)

ÌýÌýJill Slansky (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Department of Immunology and Microbiology)
ÌýÌýXiaoyun Ding (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Department of Mechanical Engineering)
ÌýÌýNew collaboration

The overarching goal of this project is to identify the biophysical properties associated with antigen-specific T cells that lead to successful adoptive cell therapies for cancer.

Extracellular vesicles mediators of stroke risk with periodontal disease

ÌýÌýKerri Font (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Associate Professor of Surgical Dentistry)
ÌýÌýChris DeSouza (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Professor of Integrative Physiology)
ÌýÌýNew collaborationÌý($50,000)

Determining the effect of circulating extracellular vesicles from adults with periodontitis on brain endothelial cell t-PA production will: a) increase our understanding of mechanisms underlying ischemic stroke risk with periodontitis; and b) identify new therapeutic targets to reduce ischemic stroke in adults with periodontal disease.

Gene-specific antisense oligonucleotide therapies for diseases of haploinsufficiency

ÌýÌýJay Hesselberth (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Associate Professor of Biochemistry and Molecular Genetics)
ÌýÌýOndrej Kostov (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Research Assistant Professor of Biochemistry)
ÌýÌýNew collaborationÌý($50,000)

We are exploring a strategy to develop antisense oligonucleotide therapies for diseases of haploinsufficiency that are gene-specific instead of mutation-specific, reducing the daunting challenge of individual ASO therapies to the identification of a minimal set (i.e., one for each gene) of ASOs that can target a gene irrespective of the nature of a specific mutation.

Immune reprogramming of myeloid cells in pancreatic islets using engineered particles

ÌýÌýRachel S. Friedman (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Department of Immunology & Microbiology)
ÌýÌýC. Wyatt Shields IV (Â鶹Ãâ·Ñ°æÏÂÔØBoulder;ÌýDepartment of Chemical and Biological Engineering)
ÌýÌýNew collaboration

This project departs from traditional methods of treating type 1 diabetes by using an engineered particle technology to sustainably reprogram islet myeloid cells to resolve inflammation and disrupt the underlying mechanisms of autoimmunity.

Noninvasive brain temperature monitoring during cardiac surgery

ÌýÌýBrett Reece (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Professor of Surgery-Cardiothoracic)
ÌýÌýZoya Popovic (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Distinguished Professor of Electrical, Computer and Energy Engineering)
ÌýÌýNew collaborationÌý($50,000)

The goal of the proposed research is to (1) develop a currently non-existent non-invasive internal body thermometer for clinical use and (2) to monitor brain temperature in order to optimize tissue protection during hypothermia while limiting the complications of cold such as coagulopathy.

Novel neurophotonics methods to access deep brain structures for decision making

ÌýÌýEmily Gibson (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Assistant Professor of Bioengineering)
ÌýÌýJuliet Gopinath (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Professor of Electrical, Computer and Energy Engineering)
ÌýÌýExisting collaborationÌý($125,000)

Neurophotonics applied to uncovering the neural mechanism of decision making in mouse models is a high-impact topic, rich for exploration. Increasing research interest, particularly at depth within the brain, makes for an exciting area both in neuroscience and photonics.

Nucleotide second messengers at the host-pathogen interface

ÌýÌýKelly S. Doran (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Department of Immunology and Microbiology)
ÌýÌýAaron T. Whiteley (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Department of Biochemistry)
ÌýÌýNew collaboration

Cyclic dinucleotides are crucial signaling molecules in the immune response to pathogens but are notoriously difficult to measure with current methodology. Using a newly developed cyclic dinucleotide biosensor platform, the Whiteley and Doran laboratories will investigate these signaling pathways during pathogenesis of Group B Streptococcus, a leading cause of invasive neonatal disease and meningitis in humans.

Optimizing a first-in-class Allosteric Eya2 Tyrosine phosphatase inhibitor for glioblastoma therapy

ÌýÌýHeide Ford (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Professor and Chair of Pharmacology and Grohne Endowed Chair in Cancer Research and Rui Zhao, Professor of Biochemistry and Molecular Genetics)
ÌýÌýXiang Wang (Â鶹Ãâ·Ñ°æÏÂÔØBoulder;ÌýAssociate Professor of Chemistry)
ÌýÌýExisting collaborationÌý($125,000)

Glioblastoma Multiforme (GBM) is one of the most aggressive and treatment-resistant cancers, accounting for nearly half of all brain cancers. This team identified a particular gene (EYA2) that is uniquely highly expressed in GBM stem cells and is essential to the success and propagation of malignant growth and will now investigate a class of lead inhibitors that can target and inhibit these cells, then optimize them to develop potent and specific EYA2 phosphatase inhibitors for GBM therapy.

Role of the gut microbiota in the pathogenesis of early-onset type 2 diabetes

ÌýÌýWei Perng (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Assistant Professor of Epidemiology)
ÌýÌýTanya Alderete (Â鶹Ãâ·Ñ°æÏÂÔØBoulder;ÌýAssistant Professor of Integrative Physiology)
ÌýÌýNew collaborationÌý($50,000)

This proposal will investigate how the gut microbiota contributes to pathogenesis of early-onset type 2 diabetes among young adult participants of the Exploring Perinatal Outcomes among CHildren (EPOCH) cohort.

Sound advice for delivering hearing health care: Evaluation of current and emerging service delivery models for hearing aids

ÌýÌýVinaya Manchaiah (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Department of Otolaryngology)
ÌýÌýAnu Sharma (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Department of Speech Language and Hearing Sciences)
ÌýÌýNew collaboration

Aging-related hearing loss, one of the most common chronic health conditions and a leading modifiable risk factor for dementia, is commonly treated with hearing aids. Our study will compare best practices for hearing aid service delivery models (i.e., professionally fit vs direct-to-consumer vs self-fit) using neurocognitive outcomes, to allow clinicians and patients to make informed hearing healthcare choices.

Novel antimicrobials for multi-drug resistant osteomyelitis: Bacteriophage stabilized for extended release by atomic layer deposition processes

ÌýÌýCarlos Catalano (Â鶹Ãâ·Ñ°æÏÂÔØAnschutz; Department of Pharmaceutical Sciences)
ÌýÌýTheodore Randolph (Â鶹Ãâ·Ñ°æÏÂÔØBoulder; Department of Chemical and Biological Engineering)
ÌýÌýNew collaboration

Osteomyelitis, or infection of the bone, is an area where multi-drug resistant nosocomial infections are particularly troublesome. This project will develop novel, controlled release formulations of bacteriophages, viruses that infect bacteria, for osteomyelitis treatment and prophylaxis.

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