Search Results - "Mertens, Fredrik"
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1
The impact of translocations and gene fusions on cancer causation
Published in Nature reviews. Cancer (01-04-2007)“…Chromosome aberrations, in particular translocations and their corresponding gene fusions, have an important role in the initial steps of tumorigenesis; at…”
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2
Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes
Published in Genes chromosomes & cancer (01-04-2016)“…Gene fusions have been described in approximately one‐third of soft tissue tumors (STT); of the 142 different fusions that have been reported, more than half…”
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3
Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics
Published in Modern pathology (01-03-2014)“…Solitary fibrous tumor (SFT) is composed of spindled to ovoid cells in a patternless architecture with prominent stromal collagen and hemangiopericytoma-like…”
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4
Deep sequencing of myxoinflammatory fibroblastic sarcoma
Published in Genes chromosomes & cancer (01-05-2020)“…Myxoinflammatory fibroblastic sarcoma (MIFS) has recurrent genetic features in the form of a translocation t(1;10)(p22‐31;q24‐25), BRAF gene fusions, and/or an…”
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5
Signatures of copy number alterations in human cancer
Published in Nature (London) (30-06-2022)“…Gains and losses of DNA are prevalent in cancer and emerge as a consequence of inter-related processes of replication stress, mitotic errors, spindle…”
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In-depth Genetic Analysis of Sclerosing Epithelioid Fibrosarcoma Reveals Recurrent Genomic Alterations and Potential Treatment Targets
Published in Clinical cancer research (01-12-2017)“…Sclerosing epithelioid fibrosarcoma (SEF) is a highly aggressive soft tissue sarcoma closely related to low-grade fibromyxoid sarcoma (LGFMS). Some tumors…”
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Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor
Published in Genes chromosomes & cancer (01-10-2013)“…Solitary fibrous tumor (SFT) is a mesenchymal neoplasm displaying variable morphologic and clinical features. To identify pathogenetically important genetic…”
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8
Most gene fusions in cancer are stochastic events
Published in Genes chromosomes & cancer (01-09-2019)“…Cancer‐associated gene fusions resulting in chimeric proteins or aberrant expression of one or both partner genes are pathogenetically and clinically important…”
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“Inflammatory Leiomyosarcoma” and “Histiocyte-rich Rhabdomyoblastic Tumor”: a clinicopathological, immunohistochemical and genetic study of 13 cases, with a proposal for reclassification as “Inflammatory Rhabdomyoblastic Tumor”
Published in Modern pathology (01-04-2021)“…Inflammatory leiomyosarcoma (ILMS), defined as “a malignant neoplasm showing smooth muscle differentiation, a prominent inflammatory infiltrate, and…”
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10
PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells
Published in Modern pathology (01-07-2020)“…Ossifying fibromyxoid tumor (OFMT) is a soft tissue tumor frequently displaying gene fusions, most of which affect the PHF1 gene. PHF1 encodes plant…”
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11
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions
Published in Leukemia (01-11-2021)“…Gene fusions have been discussed in the scientific literature since they were first detected in cancer cells in the early 1980s. There is currently no…”
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12
A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma
Published in The Journal of pathology (01-04-2014)“…Pseudomyogenic haemangioendothelioma (PHE) is an intermediate malignant vascular soft tissue tumour primarily affecting children and young adults. The…”
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13
Tetraploidization Increases the Motility and Invasiveness of Cancer Cells
Published in International journal of molecular sciences (01-09-2023)“…Polyploidy and metastasis are associated with a low probability of disease-free survival in cancer patients. Polyploid cells are known to facilitate…”
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14
Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data
Published in Genes chromosomes & cancer (01-02-2012)“…Cancer gene fusions that encode a chimeric protein are often characterized by an intragenic discontinuity in the RNA\expression levels of the exons that are 5′…”
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15
FN1-EGF gene fusions are recurrent in calcifying aponeurotic fibroma
Published in The Journal of pathology (01-03-2016)“…Calcifying aponeurotic fibroma (CAF) is a soft tissue neoplasm with a predilection for the hands and feet in children and adolescents. Its molecular basis is…”
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16
Frequent miRNA-convergent fusion gene events in breast cancer
Published in Nature communications (05-10-2017)“…Studies of fusion genes have mainly focused on the formation of fusions that result in the production of hybrid proteins or, alternatively, on…”
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17
Primary Pseudomyogenic Hemangioendothelioma of Bone
Published in The American journal of surgical pathology (01-05-2016)“…Pseudomyogenic hemangioendothelioma (PMH) is a well-recognized neoplasm that usually arises in the soft tissue; concurrent bone involvement occurs in 24% of…”
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18
Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years
Published in Nature communications (10-09-2018)“…To compare clonal evolution in tumors arising through different mechanisms, we selected three types of sarcoma—amplicon-driven well-differentiated liposarcoma…”
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Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas
Published in Genes chromosomes & cancer (01-01-2014)“…Bone and soft tissue sarcomas are a group of histologically heterogeneous and relatively uncommon tumors. To explore their genetic origins, we sequenced the…”
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Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis
Published in Genes chromosomes & cancer (01-01-2016)“…Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and adolescents. Alveolar (ARMS) and embryonal (ERMS) histologies predominate, but…”
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