Roberta Mastrantonio

ORCID: 0000-0002-1764-457X
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About
Contact & Profiles
Research Areas
  • Axon Guidance and Neuronal Signaling
  • Phagocytosis and Immune Regulation
  • Neuroblastoma Research and Treatments
  • Immune cells in cancer
  • Adenosine and Purinergic Signaling
  • Tryptophan and brain disorders
  • Immunotherapy and Immune Responses
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Polyamine Metabolism and Applications
  • S100 Proteins and Annexins
  • HIV Research and Treatment
  • Extracellular vesicles in disease
  • Autophagy in Disease and Therapy
  • Angiogenesis and VEGF in Cancer
  • Parkinson's Disease Mechanisms and Treatments
  • Cancer, Stress, Anesthesia, and Immune Response
  • Reproductive System and Pregnancy
  • Bone Tissue Engineering Materials
  • Neuroendocrine regulation and behavior
  • Silk-based biomaterials and applications
  • Toxoplasma gondii Research Studies
  • Hedgehog Signaling Pathway Studies
  • Neurogenesis and neuroplasticity mechanisms
  • Endoplasmic Reticulum Stress and Disease
  • Immune Cell Function and Interaction

Università Cattolica del Sacro Cuore
2021-2025

Agostino Gemelli University Polyclinic
2024

Istituti di Ricovero e Cura a Carattere Scientifico
2024

Roma Tre University
2014-2019

Previously, we reported that HIV-Tat elicits spermine oxidase (SMO) activity upregulation through NMDA receptor (NMDAR) stimulation in human SH-SY5Y neuroblastoma cells, thus increasing ROS generation, which turn leads to GSH depletion, oxidative stress, and reduced cell viability. In several types, can trigger an antioxidant response the transcriptional induction of stress-responsive genes regulated by nuclear factor erythroid 2-related 2 (Nrf2). Here, demonstrate Tat induces both gene...

10.1371/journal.pone.0149802 article EN cc-by PLoS ONE 2016-02-19

Neuropilin-1 (NRP1) is a transmembrane protein involved in surface receptor complexes for variety of extracellular signals. NRP1 expression human cancers associated with prominent angiogenesis and advanced progression stage. However, the molecular mechanisms underlying activity tumor microenvironment remain unclear. Notably, diffusible forms space have been reported, but their functional role poorly understood. Extracellular vesicles (EV) were isolated from conditioned media diverse cancer...

10.1186/s12964-025-02061-x article EN cc-by-nc-nd Cell Communication and Signaling 2025-01-28

The pathogenic mechanisms that underlie the progression of remote degeneration after spinal cord injury (SCI) are not fully understood. In this study, we examined relationship between endoplasmic reticulum (ER) stress and macroautophagy, hereafter autophagy, its contribution to secondary damage outcomes associated with SCI. Using a rat model hemisection at cervical level, measured ER autophagy markers in axotomized neurons red nucleus (RN). SCI animals, mRNA protein levels stress, such as...

10.1038/s41419-022-04830-9 article EN cc-by Cell Death and Disease 2022-04-20

Abstract Cytotoxic T cell (CTL) infiltration of the tumor carries potential to limit cancer progression, but their exclusion by immunosuppressive microenvironment hampers efficiency immunotherapy. Here, we show that expression axon guidance molecule Plexin-A4 (Plxna4) in CTLs, especially effector/memory CD8+ cells, is induced upon T-cell activation, sustained circulation, reduced when entering bed. Therefore, deleted Plxna4 and observed Plxna4-deficient CTLs acquired improved homing capacity...

10.1158/2326-6066.cir-21-0061 article EN cc-by-nc-nd Cancer Immunology Research 2021-11-23

Abstract Semaphorin–plexin signaling plays a major role in the tumor microenvironment (TME). In particular, Semaphorin 4D (SEMA4D) has been shown to promote growth and metastasis; however, of its high-affinity receptor Plexin-B1 (PLXNB1), which is expressed TME, poorly understood. this study, we directly targeted PLXNB1 TME triple-negative murine breast carcinoma elucidate relevance cancer progression. We found that primary metastatic dissemination were strongly reduced PLXNB1-deficient...

10.1158/2326-6066.cir-23-0289 article EN cc-by-nc-nd Cancer Immunology Research 2024-06-14

Abstract The genetic changes sustaining the development of cancers unknown primary (CUP) remain elusive. whole‐exome genomic profiling 14 rigorously selected CUP samples did not reveal specific recurring mutation in known driver genes. However, by comparing mutational landscape CUPs with that most other human tumor types, it emerged a consistent enrichment genes belonging to axon guidance KEGG pathway. In particular, G842C PlexinB2 (PlxnB2) was predicted be activating. Indeed, knocking down...

10.15252/emmm.202216104 article EN cc-by EMBO Molecular Medicine 2023-02-01

In the field of tissue engineering, recombinant protein-based biomaterials made up block polypeptides with tunable properties arising from functionalities individual domains are appealing candidates for construction medical devices. this work, we focused our attention on preparation and structural characterization nanofibers a chimeric-polypeptide-containing resilin elastin domain, designed purpose to enhance its cell-binding ability by introducing specific fibronectin-derived Arg-Gly-Asp...

10.3390/nano9111613 article EN cc-by Nanomaterials 2019-11-14

<div>Abstract<p>Semaphorin–plexin signaling plays a major role in the tumor microenvironment (TME). In particular, Semaphorin 4D (SEMA4D) has been shown to promote growth and metastasis; however, of its high-affinity receptor Plexin-B1 (PLXNB1), which is expressed TME, poorly understood. this study, we directly targeted PLXNB1 TME triple-negative murine breast carcinoma elucidate relevance cancer progression. We found that primary metastatic dissemination were strongly reduced...

10.1158/2326-6066.c.7429377.v1 preprint EN 2024-09-03

<div>Abstract<p>Semaphorin–plexin signaling plays a major role in the tumor microenvironment (TME). In particular, Semaphorin 4D (SEMA4D) has been shown to promote growth and metastasis; however, of its high-affinity receptor Plexin-B1 (PLXNB1), which is expressed TME, poorly understood. this study, we directly targeted PLXNB1 TME triple-negative murine breast carcinoma elucidate relevance cancer progression. We found that primary metastatic dissemination were strongly reduced...

10.1158/2326-6066.c.7429377 preprint EN 2024-09-03
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