Publications by authors named "Silvia Garcia-Monclus"

The EphA2 receptor tyrosine kinase is overexpressed in most solid tumors and acts as the major driver of tumorigenesis. In this study, we developed a novel approach for targeting the EphA2 receptor using a 2'-fluoro-modified pyrimidine RNA aptamer termed ATOP. We identified the ATOP EphA2 aptamer using a novel bioinformatics strategy that compared aptamers enriched during a protein SELEX using recombinant human EphA2 and a cell-internalization SELEX using EphA2-expressing MDA231 tumor cells.

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Expansion of a CAG repeat in ATXN3 causes the dominant polyglutamine disease spinocerebellar ataxia type 3 (SCA3), yet the physiological role of ATXN3 remains unclear. Here, we focus on unveiling the function of Ataxin-3 (ATXN3) in the retina, a neurological organ amenable to morphological and physiological studies. Depletion of Atxn3 in zebrafish and mice causes morphological and functional retinal alterations and, more precisely, photoreceptor cilium and outer segment elongation, cone opsin mislocalization, and cone hyperexcitation.

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Research Question: Are intrinsic or extrinsic factors associated with embryo mosaicism prevalence in IVF cycles?

Design: Retrospective cohort study of preimplantation genetic testing for aneuploidy (PGT-A) cycles carried out at a university-affiliated IVF clinic between October 2017 and October 2019. Trophectoderm biopsies were analysed by next generation sequencing. Mosaicism prevalence, type of anomaly and the chromosomes involved were analysed.

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Rhabdomyosarcoma (RMS) is the most common soft tissue malignancy in childhood and adolescence. Patients with the most aggressive histological variant have an unfavorable prognosis due to a high metastasis incidence. Lysyl oxidase-like 2 (LOXL2) is a lysyl oxidase, member of a family of extracellular matrix (ECM) crosslinking enzymes that recently have emerged as important regulators of tumor progression and metastasis.

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Soft-tissue sarcomas (STS) are an uncommon and heterogeneous group of malignancies that result in high mortality. Metastatic STS have very bad prognosis due to the lack of effective treatments. Dinaciclib is a model drug for the family of CDK inhibitors.

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Ewing sarcoma (ES) is the second most common bone malignancy affecting children and young adults with poor prognosis due to high metastasis incidence. Our group previously described that EphA2, a tyrosine kinase receptor, promotes angiogenesis in Ewing sarcoma (ES) cells via ligand-dependent signaling. Now we wanted to explore EphA2 ligand-independent activity, controlled upon phosphorylation at S897 (p-EphA2 ), as it has been linked to metastasis in several malignancies.

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Article Synopsis
  • Researchers studied how changes in DNA (called epigenetic modifications) affect a type of cancer called Ewing sarcoma.
  • They found many genes in Ewing sarcoma with different levels of DNA methylation compared to healthy tissues, which could lead to tumor growth.
  • One important gene, PTRF, was found to help fight the cancer when added back into the Ewing sarcoma cells, helping to trigger cell death in the cancer cells.
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Article Synopsis
  • Ewing sarcoma (ES) primarily affects children and young adults and is driven by the EWS/FLI1 protein, which promotes the expression of Caveolin-1 (CAV1) linked to metastasis through matrix metalloproteinase-9 (MMP-9).
  • Silencing CAV1 and IQ Motif Containing GTPase Activating Protein 1 (IQGAP1) in ES cells reduced the activation of MEK1/2 and ERK1/2, leading to decreased MMP-9 levels, migration, and invasion of cancer cells.
  • The study suggests that CAV1 and IQGAP1 are closely located at the cell edges, indicating their collaborative role in
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Ubiquitination is a relevant cell regulatory mechanism to determine protein fate and function. Most data has focused on the role of ubiquitin as a tag molecule to target substrates to proteasome degradation, and on its impact in the control of cell cycle, protein homeostasis and cancer. Only recently, systematic assays have pointed to the relevance of the ubiquitin pathway in the development and differentiation of tissues and organs, and its implication in hereditary diseases.

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Cell death can occur through different mechanisms, defined by their nature and physiological implications. Correct assessment of cell death is crucial for cancer therapy success. Sarcomas are a large and diverse group of neoplasias from mesenchymal origin.

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Article Synopsis
  • * The study identifies that the tumor suppressor gene Caveolin-1 (CAV1) is absent or minimally expressed in ARMS samples, and this silencing may be due to epigenetic changes.
  • * Reintroducing CAV1 into ARMS cell lines not only hinders their growth but also encourages muscle cell characteristics, while in live models, it leads to slower tumor growth and increased cell death, indicating its potential as a crucial tumor suppressor in
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