Shawn Baldacchino

ORCID: 0000-0001-7501-0842
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About
Contact & Profiles
Research Areas
  • Molecular Biology Techniques and Applications
  • Cancer Genomics and Diagnostics
  • Gene expression and cancer classification
  • Single-cell and spatial transcriptomics
  • PI3K/AKT/mTOR signaling in cancer
  • MicroRNA in disease regulation
  • HER2/EGFR in Cancer Research
  • RNA Interference and Gene Delivery
  • Protein Tyrosine Phosphatases
  • Circular RNAs in diseases
  • Extracellular vesicles in disease
  • Cancer-related Molecular Pathways
  • Global Cancer Incidence and Screening
  • RNA modifications and cancer
  • Cancer Cells and Metastasis
  • RNA Research and Splicing
  • Advanced Biosensing Techniques and Applications
  • Cutaneous Melanoma Detection and Management
  • FOXO transcription factor regulation
  • Chronic Lymphocytic Leukemia Research
  • Thyroid Cancer Diagnosis and Treatment
  • Clinical practice guidelines implementation
  • Brain Metastases and Treatment
  • Advanced Breast Cancer Therapies
  • 14-3-3 protein interactions

Joint Research Centre
2024

Mater Dei Hospital
2022-2023

University of Malta
2013-2022

Clotilde Théry Kenneth W. Witwer Elena Aïkawa María José Alcaraz Johnathon D. Anderson and 95 more Ramaroson Andriantsitohaina Anna Antoniou Tanina Arab Fabienne Archer Georgia K. Atkin‐Smith D. Craig Ayre Jean‐Marie Bach Daniel Bachurski Hossein Baharvand Leonora Balaj Shawn Baldacchino Natalie Bauer Amy A. Baxter Mary Bebawy Carla Beckham Apolonija Bedina Zavec Abderrahim Benmoussa Anna C. Berardi Paolo Bergese Ewa Bielska Cherie Blenkiron Sylwia Bobis‐Wozowicz Éric Boilard Wilfrid Boireau Antonella Bongiovanni Francesc E. Borràs Steffi Bösch Chantal M. Boulanger Xandra O. Breakefield Andrew Breglio Meadhbh Á. Brennan David R. Brigstock Alain Brisson Marike L. D. Broekman Jacqueline Bromberg Paulina Bryl‐Górecka Shilpa Buch Amy H. Buck Dylan Burger Sara Busatto Dominik Buschmann Benedetta Bussolati Edit I. Buzás James Brian Byrd Giovanni Camussi David R. F. Carter Sarah Caruso Lawrence W. Chamley Yu‐Ting Chang Chihchen Chen Daiwen Chen Lesley Cheng Andrew R. Chin Aled Clayton Stefano Piatto Clerici Alex Cocks Emanuele Cocucci Robert J. Coffey Anabela Cordeiro‐da‐Silva Yvonne Couch Frank A. W. Coumans Beth Coyle Rossella Crescitelli Miriã Ferreira Criado Crislyn D’Souza‐Schorey Saumya Das Amrita Datta Chaudhuri Paola de Candia Eliezer F De Santana Olivier De Wever Hernando A. del Portillo Tanguy Demaret Sarah Deville Andrew Devitt Bert Dhondt Dolores Di Vizio Lothar C. Dieterich Vincenza Dolo Ana Paula Domínguez Rubio Massimo Dominici Maurício Rocha Dourado Tom A. P. Driedonks Filipe V. Duarte Heather M. Duncan Ramon M. Eichenberger Karin M. Ekström Samir EL Andaloussi Céline Élie-Caille Uta Erdbrügger Juan Manuel Falcón‐Pérez Farah Fatima Jason E. Fish Miguel Flores‐Bellver András Försönits Annie Frelet‐Barrand

ABSTRACT The last decade has seen a sharp increase in the number of scientific publications describing physiological and pathological functions extracellular vesicles (EVs), collective term covering various subtypes cell‐released, membranous structures, called exosomes, microvesicles, microparticles, ectosomes, oncosomes, apoptotic bodies, many other names. However, specific issues arise when working with these entities, whose size amount often make them difficult to obtain as relatively...

10.1080/20013078.2018.1535750 article EN cc-by-nc Journal of Extracellular Vesicles 2018-11-23

// Rosa Drago-Ferrante 1 , Francesca Pentimalli 2 Daniela Carlisi 3 Anna De Blasio Christian Saliba 4 Shawn Baldacchino 5 James Degaetano 6 Joseph Debono 7 Gordon Caruana-Dingli Godfrey Grech Scerri 6, 8 Giovanni Tesoriere 9, 11 Antonio Giordano 10 Renza Vento 1, Riccardo Di Fiore Laboratory of Biochemistry, Department Biological, Chemical and Pharmaceutical Sciences Technologies, University Palermo, Polyclinic, Italy Oncology Research Center Mercogliano (CROM), Istituto Nazionale per lo...

10.18632/oncotarget.15960 article EN Oncotarget 2017-03-07

Abstract The present study shows that nuclear factor erythroid 2‐related 2 (NRF2) and miR‐29b‐1‐5p are two opposite forces which could regulate the fate of MDA‐MB‐231 cells, most studied triple‐negative breast cancer (TNBC) cell line. We show NRF2 activation stimulates growth markedly reduces reactive oxygen species (ROS) generation, whereas overexpression increases ROS generation proliferation. Moreover, downregulates expression, decreases p‐AKT p‐NRF2. Furthermore, induces both inhibition...

10.1002/jcp.29062 article EN Journal of Cellular Physiology 2019-07-10

The most commonly used biomarkers to predict the response of breast cancer patients therapy are oestrogen receptor (ER), progesterone (PgR), and human epidermal growth factor 2 (HER2). Patients positive for these eligible specific therapies such as endocrine treatment in event ER PgR positivity, monoclonal antibody, trastuzumab, case HER2-positive patients. who negative three biomarkers, so-called triple negatives, however, derive little benefit from associated with a worse prognosis....

10.1186/1878-5085-5-3 article EN cc-by The EPMA Journal 2014-01-25

Abstract Triple‐negative breast cancer (TNBC) is a form of BC characterized by high aggressiveness and therapy resistance probably determined stem cells. MCL1 an antiapoptotic Bcl‐2 family member that could limit the efficacy anticancer agents as recombinant human tumor necrosis factor related apoptosis‐inducing ligand (rh‐TRAIL). Here, we investigated expression in TNBC tissues We found differentially expressed (upregulated or downregulated) tissues. Furthermore, comparison to mammary...

10.1002/jcp.28479 article EN Journal of Cellular Physiology 2019-03-25

Nucleic acid degradation in archival tissue, tumor heterogeneity, and a lack of fresh frozen tissue specimens can negatively impact cancer diagnostic services pathology laboratories worldwide. Gene amplification expression testing using material or that requires transportation to servicing laboratories, needs more robust accurate test adapted current clinical workflows. Our research team optimized the use Invitrogen™ QuantiGene™ Plex Assay (Thermo Fisher Scientific) quantify RNA branched-DNA...

10.3791/57148 article EN Journal of Visualized Experiments 2018-08-01

Diagnosing thyroid carcinoma is not always easy on basic haemtoxylin and eosin staining since nuclear features are inconsistent controversial. In view of this, studies the role immunohistochemical markers in diagnosis malignant necessary. Proposed for papillary cancer include Hector Battifora mesothelial-1 (HBME-1), Galectin-3 (Gal-3) which have been studied this project. Immunohistochemical fifty-eight formalin-fixed paraffin embedded surgically removed tissue from years 2008 2013 was...

10.3390/endocrines3020021 article EN cc-by Endocrines 2022-05-11

The use of archival formalin-fixed paraffin-embedded (FFPE) material to analyse gene expression is limited by the low quality extracted RNA.In this paper, we utilised an RNA based assay quantify luminal and basal markers, together with ERBB2 probes, in FFPE tissue from 2009 2010, all which had clinical therapeutic information more than 5 years.Receptor status patients was characterised using QuantiGene® Plex 100% concordance immunohistochemical (IHC) fluorescence situ hybridisation (FISH)...

10.4172/2155-9929.s8-016 article EN Journal of Molecular Biomarkers & Diagnosis 2016-01-01

Nucleic acid degradation in archival tissue, tumor heterogeneity, and a lack of fresh frozen tissue specimens can negatively impact cancer diagnostic services pathology laboratories worldwide. Gene amplification expression testing using material or that requires transportation to servicing laboratories, needs more robust accurate test adapted current clinical workflows. Our research team optimized the use Invitrogen™ QuantiGene™ Plex Assay (Thermo Fisher Scientific) quantify RNA branched-DNA...

10.3791/57148-v article EN Journal of Visualized Experiments 2018-08-01

CIP2A is emerging as an oncoprotein overexpressed commonly across many tumours and generally correlated with higher tumour grade therapeutic resistance. drives oncogenic potential through inhibiting protein phosphatase 2A, stabilizing MYC, promoting epithelial-to-mesenchymal transition, although further biological mechanisms for are yet to be defined. expression was studied by immunohistochemistry in oestrogen receptor–positive primary breast cancers (n = 250) obtained from the Leeds Tissue...

10.1177/1010428317722064 article EN cc-by-nc Tumor Biology 2017-10-01

The characterisation of the molecular mechanism disease allows classification patients into subtypes and potentially identifies specific targets for therapeutic intervention. Tyrosine kinase mutations are central to targeted therapy. Investigation deregulation within particular patient groups, has led identification mutant tyrosine kinases associated with progression therapy modulation. Biomarker-specific therapies emerged, taking a leading role in guided-therapy. extensive use inhibitors...

10.1186/1878-5085-5-s1-a26 article EN cc-by The EPMA Journal 2014-02-01
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