Not all cancer patients need chemo — Ataraxis AI raised $20M to personalize treatment
Ataraxis AI has raised a $20.4 million Series A to make cancer treatment more personalized.
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Ataraxis AI has raised a $20.4 million Series A to make cancer treatment more personalized.
© 2024 TechCrunch. All rights reserved. For personal use only.
Nature, Published online: 05 February 2025; doi:10.1038/s41586-024-08398-6
PELO–HBS1L and SKI complexes in the human mRNA quality control pathway exhibit a synthetic lethal interaction and may represent novel targets for the development of cancer therapies.Nat Comput Sci. 2025 Feb 7. doi: 10.1038/s43588-024-00764-8. Online ahead of print.
ABSTRACT
Large-scale whole-genome sequencing (WGS) studies have improved our understanding of the contributions of coding and noncoding rare variants to complex human traits. Leveraging association effect sizes across multiple traits in WGS rare variant association analysis can improve statistical power over single-trait analysis, and also detect pleiotropic genes and regions. Existing multi-trait methods have limited ability to perform rare variant analysis of large-scale WGS data. We propose MultiSTAAR, a statistical framework and computationally scalable analytical pipeline for functionally informed multi-trait rare variant analysis in large-scale WGS studies. MultiSTAAR accounts for relatedness, population structure and correlation among phenotypes by jointly analyzing multiple traits, and further empowers rare variant association analysis by incorporating multiple functional annotations. We applied MultiSTAAR to jointly analyze three lipid traits in 61,838 multi-ethnic samples from the Trans-Omics for Precision Medicine (TOPMed) Program. We discovered and replicated new associations with lipid traits missed by single-trait analysis.
PMID:39920506 | DOI:10.1038/s43588-024-00764-8
Global Spine J. 2025 Jan;15(1_suppl):16S-28S. doi: 10.1177/21925682231222012.
ABSTRACT
STUDY DESIGN: Narrative review.
OBJECTIVES: This article aims to provide a narrative review of the current state of research for liquid biopsy in spinal tumors and to discuss the potential application of liquid biopsy in the clinical management of patients with spinal tumors.
METHODS: A comprehensive review of the literature was performed using PubMed, Google Scholar, Medline, Embase and Cochrane databases, and the review was limited to articles of English language. All the relevant articles which were identified to be related to liquid biomarker study in spinal tumors, were studied in full text.
RESULTS: Liquid biopsy has revolutionized the field of precision medicine by guiding personalized clinical management of cancer patients based on the liquid biomarker status. In recent years, more research has been done to investigate its potential utilization in patients with tumors from the spine. Herein, we review the liquid biomarkers that have been proposed in different spine malignancies including chordoma, chondrosarcoma, Ewing sarcoma, osteosarcoma, astrocytoma and ependymoma. We also discuss the wide window of opportunity to utilize these liquid biomarkers in diagnosis, treatment response, monitoring, and detection of minimal residual disease in patients with spinal tumors.
CONCLUSIONS: Liquid biomarkers, especially blood-derived circulating tumor DNA, has a promising clinical utility as they are disease-specific, minimally invasive, and the procedure is repeatable. Prospective studies with larger populations are needed to fully establish its use in the setting of spinal tumors.
PMID:39801114 | PMC:PMC11726521 | DOI:10.1177/21925682231222012
Nature, Published online: 23 December 2024; doi:10.1038/s41586-024-08555-x
Author Correction: π-HuB: the proteomic navigator of the human bodyNature, Published online: 27 March 2024; doi:10.1038/s41586-024-07239-w
We introduce multinucleic acid interaction mapping in single cells (MUSIC), for concurrent profiling of multiplex chromatin interactions, gene expression and RNA–chromatin associations within individual nuclei, as a tool for exploring chromatin architecture and transcription.Nature, Published online: 08 February 2024; doi:10.1038/s41586-024-07051-6
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico CityNature, Published online: 18 December 2023; doi:10.1038/s41586-023-06961-1
Publisher Correction: Slide-tags enables single-nucleus barcoding for multimodal spatial genomicsNature, Published online: 13 December 2023; doi:10.1038/s41586-023-06837-4
Slide-tags enables multiomic sequencing of single cells and their localization within tissues.Nature Biotechnology, Published online: 06 February 2023; doi:10.1038/s41587-022-01652-0
A six-letter sequencing workflow can simultaneously detect genetic and epigenetic bases.