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Biology subjects

Hirsch, M. G.

Publications and source records attributed to Hirsch, M. G..

3 recordsLinked to original sources

Combined inference of known and novel mutational signatures with ReDeNovo

Mutational signatures represent characteristic mutational patterns imprinted on the genome by mutagenic processes. They can provide information about the impact of the environmental and endogenous cellular processes on tumor mutations and can suggest treatment. Analysis of presence and strength of mutational signatures in cancer genomes has become a cornerstone in analysis of new and legacy cancer data. However, a precise inference of novel (de novo) signatures requires a large set of genomes, and methods focusing on estimating the presence of previously defined signatures are unable to uncover potential novel signatures that might emerge in new data. Thus, reliable methods to address these challenges are needed. We formally define the Combined Mutational Signature Inference Problem (CMSI) for the identification of known signatures and the inference of novel signatures in cancer data. CMSI represents non-convex optimization, and we provide a heuristic algorithm, ReDeNovo, to solve it efficiently. We extensively validated ReDeNovo on simulated data, evaluating its ability to precisely estimate presence and exposure to known signatures and to discover of novel signatures. On both tasks ReDeNovo outperformed existing approaches. In real biological data, ReDeNovo identified signatures missed by previous analyses and defined a new signature related to UV light exposure. ReDeNovo method provides a new and powerful tool to uncover mutational signatures. ReDeNovo is available from https://github.com/ncbi/redenovo.

genomics↗

Connecting spatial regions to clinical phenotypes by transferring knowledge from bulk patient data

Spatially resolved transcriptomics (SRT) technology has enabled a new level of knowledge about tumors. Many critical tumor properties, such as invasiveness and growth, depend on both specific transcriptomic changes in tumor cells and the tumor microenvironment. However, computational methods to study clinical phenotypes of spatial regions, such as hazard and drug response, have not yet been developed. Since clinical phenotypes are measured at the patient level and not at the level of spatial regions, such a method would require transferring knowledge from the patient level domain to the spot level domain. To overcome this challenge, we developed SpacePhenotyper. Our approach uses algebraic spectral techniques to transfer the predictive relationship between gene expression and clinical phenotypes from bulk gene expression data to SRT data. Our approach captures a gene expression pattern that is predictive of the phenotype of interest in the form of a vector, the "Eigen-Patient," which is then used to quantify the phenotype in spatial spots. After extensively validating SpacePhenotyper on simulated and real data, we utilize it to study how the spatial heterogeneity of breast cancer tumors influences residual cancer burden after treatment. By assigning relative quantities of clinical phenotypes to spatial locations, SpacePhenotyper has proven a powerful tool for the identification and interpretation of transcriptional changes over spatial regions and of spatially-regulated patterns of cellular states. SpacePhenotyper is implemented in Python. The source code and data sets used for and generated during this study are available at https://github.com/ncbi/SpacePhenotyper

cancer biology↗

Stochastic modelling of single-cell gene expression adaptation reveals non-genomic contribution to evolution of tumor subclones

Cancer progression is an evolutionary process driven by the selection of cells adapted to gain growth advantage. We present the first formal study on the adaptation of gene expression in subclonal evolution. We model evolutionary changes in gene expression as stochastic Ornstein-Uhlenbeck processes, jointly leveraging the evolutionary history of subclones and single-cell expression data. Applying our model to sublines derived from single cells of a mouse melanoma revealed that sublines with distinct phenotypes are underlined by different patterns of gene expression adaptation, indicating non-genetic mechanisms of cancer evolution. Interestingly, sublines previously observed to be resistant to anti-CTLA-4 treatment showed adaptive expression of genes related to invasion and non-canonical Wnt signaling, whereas sublines that responded to treatment showed adaptive expression of genes related to proliferation and canonical Wnt signaling. Our results suggest that clonal phenotypes emerge as the result of specific adaptivity patterns of gene expression.

cancer biology↗