Vanessa Desantis

ORCID: 0000-0003-1942-2601
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Multiple Myeloma Research and Treatments
  • Protein Degradation and Inhibitors
  • MicroRNA in disease regulation
  • Histone Deacetylase Inhibitors Research
  • Chemokine receptors and signaling
  • Peptidase Inhibition and Analysis
  • Vasculitis and related conditions
  • Extracellular vesicles in disease
  • Nanoparticle-Based Drug Delivery
  • RNA Interference and Gene Delivery
  • Atherosclerosis and Cardiovascular Diseases
  • CAR-T cell therapy research
  • Cancer Mechanisms and Therapy
  • Fibroblast Growth Factor Research
  • Autophagy in Disease and Therapy
  • Atrial Fibrillation Management and Outcomes
  • Mast cells and histamine
  • Immunodeficiency and Autoimmune Disorders
  • Chronic Lymphocytic Leukemia Research
  • Biomarkers in Disease Mechanisms
  • Ubiquitin and proteasome pathways
  • Cell Adhesion Molecules Research
  • Dendrimers and Hyperbranched Polymers
  • Cardiac tumors and thrombi
  • Systemic Lupus Erythematosus Research

University of Bari Aldo Moro
2016-2025

Azienda Universitaria Ospedaliera Consorziale - Policlinico Bari
2018-2020

Abstract Aberrant microRNA (miR) expression has an important role in tumour progression, but its involvement bone marrow fibroblasts of multiple myeloma patients remains undefined. We demonstrate that a specific miR profile parallels the transition from monoclonal gammopathy undetermined significance (MGUS) to myeloma. Overexpression miR‐27b‐3p and miR‐214‐3p triggers proliferation apoptosis resistance via FBXW7 PTEN/AKT/GSK3 pathways, respectively. Transient transfection inhibitors...

10.1002/path.5187 article EN The Journal of Pathology 2018-10-25

Cell adhesion in the multiple myeloma (MM) microenvironment has been recognized as a major mechanism of MM cell survival and development drug resistance. Here we addressed hypothesis that protein junctional molecule-A (JAM-A) may represent novel target clinical biomarker MM. We evaluated JAM-A expression lines 147 patient bone marrow aspirates biopsies at different disease stages. Elevated levels patient-derived plasma cells were correlated with poor prognosis. Moreover, circulating soluble...

10.1038/leu.2017.287 article EN cc-by-nc-sa Leukemia 2017-09-28

The mammalian Target of Rapamycin (mTOR) is an intracellular serine/threonine kinase that mediates metabolism, cell survival and actin rearrangement. mTOR made two independent complexes, mTORC1 mTORC2, activated by the scaffold proteins RAPTOR RICTOR, respectively. activation triggers protein synthesis autophagy inhibition, while mTORC2 promotes progression, survival, reorganization, drug resistance through AKT hyper-phosphorylation on Ser473. Due to pivotal role in tumor cells, we evaluated...

10.18632/oncotarget.25003 article EN Oncotarget 2018-04-16

Abstract Multiple myeloma, the second most common hematologic malignancy, frequently relapses because of chemotherapeutic resistance. Fibroblast growth factors (FGF) act as proangiogenic and mitogenic cytokines in multiple myeloma. Here, we demonstrate that autocrine FGF/FGFR axis is essential for myeloma cell survival progression by protecting cells from oxidative stress–induced apoptosis. In keeping with hypothesis intracellular redox status can be a target cancer therapy, blockade FGF...

10.1158/0008-5472.can-19-2714 article EN Cancer Research 2020-02-24

Abstract Inborn errors of immunity (IEI) entail a diverse group disorders resulting from hereditary or de novo mutations in single genes, leading to immune dysregulation. This study explores the clinical utility next-generation sequencing (NGS) techniques diagnosing monogenic defects. Eight patients attending immunodeficiency clinic and with unclassified antibody deficiency were included analysis. Clinical records, characteristics, family histories reviewed, target gene panel (TGP) was...

10.1007/s11739-025-03871-0 article EN cc-by Internal and Emergency Medicine 2025-01-28

Multiple Myeloma is driven by clonal plasma cell (cPC)-intrinsic factors and changes in the tumorigenic microenvironment (TME). To investigate if residual polyclonal PCs (pPCs) are disrupted, single-cell (sc) RNAseq sc B-cell receptor analysis were applied a cohort of 46 samples with PC dyscrasias 21 healthy donors (HDs). Out n=234,789 PCs, 64,432 genotypically identified as pPCs frequencies decreasing over different disease stages, from 23.66% monoclonal gammopathy undetermined significance...

10.1182/blood.2024025643 article EN cc-by-nc-nd Blood 2025-02-26

Dupilumab, a monoclonal antibody targeting the interleukin (IL)-4 receptor alpha subunit and IL-13, has markedly advanced treatment of atopic conditions such as dermatitis, asthma, chronic rhinosinusitis. However, its expanding use brought increased attention to range ocular adverse events—conjunctivitis, blepharitis, keratitis, corneal ulcers, cicatricial conjunctivitis—that remain underrecognized frequently underestimated in clinical practice. These manifestations often emerge patients...

10.3390/jcm14072487 article EN Journal of Clinical Medicine 2025-04-05

The investigational drug MP0250 is a multi-specific DARPin® molecule that simultaneously binds and neutralizes VEGF HGF with high specificity affinity. Here we studied the antiangiogenic effects of in multiple myeloma (MM). In endothelial cells (EC) isolated from bone marrow (BM) MM patients (MMEC) reduces VEGFR2 cMet phosphorylation affects their downstream signaling cascades. influences secretory profile MMEC inhibits vitro angiogenic activities (spontaneous chemotactic migration,...

10.18632/oncotarget.24351 article EN Oncotarget 2018-01-30

Interactions of multiple myeloma (MM) cells with endothelial (ECs) enhance angiogenesis and MM progression. Here, we investigated the role Notch signaling in cross talk between ECs enabling angiogenesis. MMECs showed higher expression Jagged1/2 ligands, activated Notch1/2 receptors, Hes1/Hey1 target genes than from monoclonal gammopathy undetermined significance patients, suggesting that homotypic activation pathway occurs MM. co-cultured triggered these through a cell-to-cell...

10.1016/j.neo.2018.10.011 article EN cc-by-nc-nd Neoplasia 2018-12-05
Coming Soon ...