27 research outputs found

    Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context

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    Long noncoding RNAs (lncRNAs) are commonly dys-regulated in tumors, but only a handful are known toplay pathophysiological roles in cancer. We inferredlncRNAs that dysregulate cancer pathways, onco-genes, and tumor suppressors (cancer genes) bymodeling their effects on the activity of transcriptionfactors, RNA-binding proteins, and microRNAs in5,185 TCGA tumors and 1,019 ENCODE assays.Our predictions included hundreds of candidateonco- and tumor-suppressor lncRNAs (cancerlncRNAs) whose somatic alterations account for thedysregulation of dozens of cancer genes and path-ways in each of 14 tumor contexts. To demonstrateproof of concept, we showed that perturbations tar-geting OIP5-AS1 (an inferred tumor suppressor) andTUG1 and WT1-AS (inferred onco-lncRNAs) dysre-gulated cancer genes and altered proliferation ofbreast and gynecologic cancer cells. Our analysis in-dicates that, although most lncRNAs are dysregu-lated in a tumor-specific manner, some, includingOIP5-AS1, TUG1, NEAT1, MEG3, and TSIX, synergis-tically dysregulate cancer pathways in multiple tumorcontexts

    Pan-cancer Alterations of the MYC Oncogene and Its Proximal Network across the Cancer Genome Atlas

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    Although theMYConcogene has been implicated incancer, a systematic assessment of alterations ofMYC, related transcription factors, and co-regulatoryproteins, forming the proximal MYC network (PMN),across human cancers is lacking. Using computa-tional approaches, we define genomic and proteo-mic features associated with MYC and the PMNacross the 33 cancers of The Cancer Genome Atlas.Pan-cancer, 28% of all samples had at least one ofthe MYC paralogs amplified. In contrast, the MYCantagonists MGA and MNT were the most frequentlymutated or deleted members, proposing a roleas tumor suppressors.MYCalterations were mutu-ally exclusive withPIK3CA,PTEN,APC,orBRAFalterations, suggesting that MYC is a distinct onco-genic driver. Expression analysis revealed MYC-associated pathways in tumor subtypes, such asimmune response and growth factor signaling; chro-matin, translation, and DNA replication/repair wereconserved pan-cancer. This analysis reveals insightsinto MYC biology and is a reference for biomarkersand therapeutics for cancers with alterations ofMYC or the PMN

    Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas

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    This integrated, multiplatform PanCancer Atlas study co-mapped and identified distinguishing molecular features of squamous cell carcinomas (SCCs) from five sites associated with smokin

    Spatial Organization and Molecular Correlation of Tumor-Infiltrating Lymphocytes Using Deep Learning on Pathology Images

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    Beyond sample curation and basic pathologic characterization, the digitized H&E-stained images of TCGA samples remain underutilized. To highlight this resource, we present mappings of tumorinfiltrating lymphocytes (TILs) based on H&E images from 13 TCGA tumor types. These TIL maps are derived through computational staining using a convolutional neural network trained to classify patches of images. Affinity propagation revealed local spatial structure in TIL patterns and correlation with overall survival. TIL map structural patterns were grouped using standard histopathological parameters. These patterns are enriched in particular T cell subpopulations derived from molecular measures. TIL densities and spatial structure were differentially enriched among tumor types, immune subtypes, and tumor molecular subtypes, implying that spatial infiltrate state could reflect particular tumor cell aberration states. Obtaining spatial lymphocytic patterns linked to the rich genomic characterization of TCGA samples demonstrates one use for the TCGA image archives with insights into the tumor-immune microenvironment

    Integrated Genomic Analysis of the Ubiquitin Pathway across Cancer Types

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    Protein ubiquitination is a dynamic and reversibleprocess of adding single ubiquitin molecules orvarious ubiquitin chains to target proteins. Here,using multidimensional omic data of 9,125 tumorsamples across 33 cancer types from The CancerGenome Atlas, we perform comprehensive molecu-lar characterization of 929 ubiquitin-related genesand 95 deubiquitinase genes. Among them, we sys-tematically identify top somatic driver candidates,including mutatedFBXW7with cancer-type-specificpatterns and amplifiedMDM2showing a mutuallyexclusive pattern withBRAFmutations. Ubiquitinpathway genes tend to be upregulated in cancermediated by diverse mechanisms. By integratingpan-cancer multiomic data, we identify a group oftumor samples that exhibit worse prognosis. Thesesamples are consistently associated with the upre-gulation of cell-cycle and DNA repair pathways, char-acterized by mutatedTP53,MYC/TERTamplifica-tion, andAPC/PTENdeletion. Our analysishighlights the importance of the ubiquitin pathwayin cancer development and lays a foundation fordeveloping relevant therapeutic strategies

    The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

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    Machine Learning Identifies Stemness Features Associated with Oncogenic Dedifferentiation.

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    Cancer progression involves the gradual loss of a differentiated phenotype and acquisition of progenitor and stem-cell-like features. Here, we provide novel stemness indices for assessing the degree of oncogenic dedifferentiation. We used an innovative one-class logistic regression (OCLR) machine-learning algorithm to extract transcriptomic and epigenetic feature sets derived from non-transformed pluripotent stem cells and their differentiated progeny. Using OCLR, we were able to identify previously undiscovered biological mechanisms associated with the dedifferentiated oncogenic state. Analyses of the tumor microenvironment revealed unanticipated correlation of cancer stemness with immune checkpoint expression and infiltrating immune cells. We found that the dedifferentiated oncogenic phenotype was generally most prominent in metastatic tumors. Application of our stemness indices to single-cell data revealed patterns of intra-tumor molecular heterogeneity. Finally, the indices allowed for the identification of novel targets and possible targeted therapies aimed at tumor differentiation

    Molecular characterization and clinical relevance of metabolic expression subtypes in human cancers.

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    Metabolic reprogramming provides critical information for clinical oncology. Using molecular data of 9,125 patient samples from The Cancer Genome Atlas, we identified tumor subtypes in 33 cancer types based on mRNA expression patterns of seven major metabolic processes and assessed their clinical relevance. Our metabolic expression subtypes correlated extensively with clinical outcome: subtypes with upregulated carbohydrate, nucleotide, and vitamin/cofactor metabolism most consistently correlated with worse prognosis, whereas subtypes with upregulated lipid metabolism showed the opposite. Metabolic subtypes correlated with diverse somatic drivers but exhibited effects convergent on cancer hallmark pathways and were modulated by highly recurrent master regulators across cancer types. As a proof-of-concept example, we demonstrated that knockdown of SNAI1 or RUNX1—master regulators of carbohydrate metabolic subtypes-modulates metabolic activity and drug sensitivity. Our study provides a system-level view of metabolic heterogeneity within and across cancer types and identifies pathway cross-talk, suggesting related prognostic, therapeutic, and predictive utility

    Functional Imaging in Diagnostic of Orthopedic Implant-Associated Infections

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    Surgeries’ sterile conditions and perioperative antibiotic therapies decrease implant associated infections rates significantly. However, up to 10% of orthopedic devices still fail due to infections. An implant infection generates a high socio-economic burden. An early diagnosis of an infection would significantly improve patients’ outcomes. There are numerous clinical tests to diagnose infections. The “Gold Standard” is a microbiological culture, which requires an invasive sampling and lasts up to several weeks. None of the existing tests in clinics alone is sufficient for a conclusive diagnosis of an infection. Meanwhile, there are functional imaging modalities, which hold the promise of a non-invasive, quick, and specific infection diagnostic. This review focuses on orthopedic implant-associated infections, their pathogenicity, diagnosis and functional imaging

    Game as a promotion for average preschool children comunication skills

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    Darba autore: Inga Potapova Darba zinātniskā vadītāja: Dr. Paed. Antra Randoha Pētnieciskā darba temats: ”Rotaļa-vidējā pirmsskolas vecuma bērnu saskarsmes prasmju sekmētāja.” Pētījuma mērķis: Izzināt un praktiski pētīt vidējā pirmsskolas vecuma bērnu saskarsmes prasmju sekmēšanas iespējas rotaļās. Pētījuma uzdevumi: 1. analizēt dažādu autoru pedagoģisko, psiholoģisko literatūru par vidējā pirmsskolas vecuma bērnu saskarsmes prasmju attīstību rotaļās; 2. praktiski pētīt un analizēt bērna saskarsmes prasmju attīstību rotaļās; 3. apkopot rezultātus un izdarīt secinājumus. Pētījuma hipotēze: saskarsmes prasmes noritēs veiksmīgi, ja pedagogs sekmēs to attīstību ievērojot bērna vecuma un individuālās attīstības likumsakarības. Izmantos atbilstošas mācību metodes, un kā līdzekli to veidošanas procesā izmantos rotaļu. Pētījuma metodes: 1. teorētiskā metode: pedagoģiskās un psiholoģiskās literatūras analīze; 2. empīriskā metode: anketēšana, pedagoģiskais novērojums, datu anlīze. Kvalifikācijas darbam ir divas daļas - teorētiskā daļa, kurā tiek analizēta dažādu autoru pedagoģiskā un psiholoģiskā literatūra. Tiek skaidrots-kas ir saskarsme, kā tā veidojas. Tiek teorētiski analizētas vidējā pirmsskolas vecuma bērnu attīstības likumsakarību raksturojums. Tiek analizēta rotaļa kā saskarsmes prasmju sekmētāja. Empīriskajā metodē tiek pētītas bērna saskarsmes prasmes rotaļā. Apkopot rezultātus, noskaidrot rotaļu ietekmi uz bērnu saskarsmes prasmēm. Izdarīt secinājumus.Author: Inga Potapova Scientific supervisor: Dr. Paed. Antra Randoha Theme of the research: ”Game as a promotion for avarge pre-school childrens communication skills.” Aim of the research: To cognize and research avarge pre-school childrens communication skill development while using games as a promotion. Resarch tasks: 1.To analyze the pedagogical and psychological literature of various authors about avarge pre-school children development of communication skills in games. 2. Practically research and analyze the development of child's communication skills in games; 3. Summarize the results and draw conclusions Research hypothesis: Communication skills will be successful if the teacher contributes to their development, taking into account the regularities of the child's age and individual development. Appropriate teaching methods will be used, and the playground will be used as a means of developing them. Research methods: 1. theoretical method: analysis of pedagogical and psychological literature; 2. empirical method: questioning, pedagogical observation, data analyzing. The qualification work has two parts - the theoretical part, which analyzes pedagogical and psychological literature of different authors. It is explained what is communication, how it is developed. Theoretically analyzed avarge pre-school children regularities development . The game is analyzed as an interpersonal skills facilitator.The empirical method examines the child's communication skills in a play. To sum up the results, find out the effects of the games on children's communication skills. Draw conclusions
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