Helili, Z. | Search bioRxiv

bioRxiv2022

The Children's Brain Tumor Network (CBTN) - Accelerating Research in Pediatric Central Nervous System Tumors through Collaboration and Open Science

Pediatric brain tumors are the leading cause of cancer-related death in children in the United States and contribute a disproportionate number of potential years of life lost compared to adult cancers. Moreover, survivors frequently suffer long-term side effects, including secondary cancers. The Childrens Brain Tumor Network (CBTN) is a multi-institutional international clinical research consortium created to advance therapeutic development through the collection and rapid distribution of biospecimens and data via open-science research platforms for real-time access and use by the global research community. The CBTNs 32 member institutions utilize a shared regulatory governance architecture at the Childrens Hospital of Philadelphia to accelerate and maximize the use of biospecimens and data. As of August 2022, CBTN has enrolled over 4,700 subjects, over 1,500 parents, and collected over 65,000 biospecimen aliquots for research. Additionally, over 80 preclinical models have been developed from collected tumors. Multi-omic data for over 1,000 tumors and germline material is currently available with data generation for > 5,000 samples underway. To our knowledge, CBTN provides the largest open-access pediatric brain tumor multi-omic dataset annotated with longitudinal clinical and outcome data, imaging, associated biospecimens, child-parent genomic pedigrees, and in vivo and in vitro preclinical models. Empowered by NIH-supported platforms such as the Kids First Data Resource and the Childhood Cancer Data Initiative, the CBTN continues to expand the resources needed for scientists to accelerate translational impact for improved outcomes and quality of life for children with brain and spinal cord tumors.

cancer biology↗

bioRxiv2018

Fast temporal dynamics and causal relevance of face processing in the human temporal cortex

Recordings with a large number of intracranial electrodes in eight neurosurgical subjects offered a unique opportunity to examine the fast temporal dynamics of face processing simultaneously across a relatively large extent of the human temporal cortex (TC). Measuring the power of slow oscillatory bands of activity ({theta}, , {beta}, and {gamma}) as well as High-Frequency Broadband (HFB, 70-177 Hz) signal, we found that the HFB showed the strongest univariate and multivariate changes in response to face compared to non-face stimuli. Using the HFB signal as a surrogate marker for local cortical engagement, we identified recording sites with selective responses to faces that were anatomically consistent across subjects and responded with graded strength to human, mammal, bird, and marine animal faces. Importantly, the most face selective sites were located more posteriorly and responded earlier than those with less selective responses to faces. Using machine learning based methods, we demonstrated that a sparse model focusing on information from the human face selective sites performed as well as, or better than, anatomically distributed models of face processing when discriminating faces from non-faces stimuli. Lastly, we identified the posterior fusiform (pFUS) site as causally the most relevant node for inducing distortion of face perception by direct electrical stimulation. Our findings support the notion of face information being processed first in the most selective sites - that are anatomically discrete and localizable within individual brains and anatomically consistent across subjects - which is then distributed in time to less selective anterior temporal sites within a time window that is too fast to be detected by current neuroimaging methods. The new information about the fast spatio-temporal dynamics of face processing across multiple sites of the human brain provides a new common ground for unifying the seemingly contradictory modular and distributed models of face processing in the human brain.

neuroscience↗