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Wlasnowolski, M.

Publications and source records attributed to Wlasnowolski, M..

3 recordsLinked to original sources

Unveiling epigenetic regulatory elements associated with breast cancer development

Breast cancer is the most common cancer in women and the 2nd most common cancer worldwide, yearly impacting over 2 million females and causing 650 thousand deaths. It has been widely studied, but its epigenetic variation is not entirely unveiled. We aimed to identify epigenetic mechanisms impacting the expression of breast cancer related genes to detect new potential biomarkers and therapeutic targets. We considered The Cancer Genome Atlas database with over 800 samples and several omics datasets such as mRNA, miRNA, DNA methylation, which we used to select 2701 features that were statistically significant to differ between cancer and control samples using the Monte Carlo Feature Selection and Interdependency Discovery algorithm, from an initial total of 417,486. Their biological impact on cancerogenesis was confirmed using: statistical analysis, natural language processing, linear and machine learning models as well as: transcription factors identification, drugs and 3D chromatin structure analyses. Classification of cancer vs control samples on the selected features returned high classification weighted Accuracy from 0.91 to 0.98 depending on feature-type: mRNA, miRNA, DNA methylation, and classification algorithm. In general, cancer samples showed lower expression of differentially expressed genes and increased {beta}-values of differentially methylated sites. We identified mRNAs whose expression is well explained by miRNA expression and differentially methylated sites {beta}-values. We recognized differentially methylated sites possibly affecting NRF1 and MXI1 transcription factors binding, causing a disturbance in NKAPL and PITX1 expression, respectively. Our 3D models showed more loosely packed chromatin in cancer. This study successfully points out numerous possible regulatory dependencies.

cancer biology↗

cudaMMC - GPU-enhanced Multiscale Monte Carlo Chromatin 3D Modelling

MotivationInvestigating the 3D structure of chromatin provides new insights into transcriptional regulation. With the advancements in 3C new-sequencing techniques such as ChiA-PET and Hi-C, there has been a substantial increase in the volume of collected data, necessitating faster algorithms for chromatin spatial modelling. This study presents the cudaMMC method, which utilises the Simulated Annealing Monte Carlo approach extended by GPU-accelerated computing to generate ensembles of chromatin 3D structures efficiently. ResultsThe cudaMMC calculations demonstrate significantly faster performance and lower (better) model scores compared to our previous method on the same workstation. cudaMMC substantially reduces the computation time required for generating ensembles of large chromatin models, making it an invaluable tool for studying chromatin spatial conformation. AvailabilityOpen-source software and manual and sample data are freely available on https://github.com/SFGLab/cudaMMC ContactDariusz.Plewczynski@pw.edu.pl

bioinformatics↗

Spatial Chromatin Architecture Alteration by Structural Variations in Human Genomes at Population Scale

This genome-wide study is focused on the impact of structural variants identified in individuals from 26 human populations onto three-dimensional structures of their genomes. We assess the tendency of structural variants to accumulate in spatially interacting genomic segments and design a high-resolution computational algorithm to model the 3D conformational changes resulted by structural variations. We show that differential gene transcription is closely linked to variation in chromatin interaction networks mediated by RNA polymerase II. We also demonstrate that CTCF-mediated interactions are well conserved across population, but enriched with disease-associated SNPs. Altogether, this study assesses the critical impact of structural variants on the higher order organization of chromatin folding and provides unique insight into the mechanisms regulating gene transcription at the population scale, among which the local arrangement of chromatin loops seems to be the leading one. It is the first insight into the variability of the human 3D genome at the population scale.

genomics↗