Enzymatic Spermine Metabolites Induce Apoptosis Associated with Increase of p53, caspase-3 and miR-34a in Both Neuroblastoma Cells, SJNKP and the N-Myc-Amplified Form IMR5

Autor: Pasquale Fino, Gabriella Schiera, Gianluca Canettieri, Yuta Kanamori, Italia Di Liegro, Enzo Agostinelli, Patrizia Proia, Jessica Gasparello, Roberto Gambari, Alessia Finotti, Laura Di Magno, Carlo Maria Di Liegro, Paola Tirassa, Fabio Timeus, Tomoaki Tahara, Antonio Greco
Přispěvatelé: Kanamori Y., Finotti A., Di Magno L., Canettieri G., Tahara T., Timeus F., Greco A., Tirassa P., Gasparello J., Fino P., Di Liegro C.M., Proia P., Schiera G., Di Liegro I., Gambari R., Agostinelli E.
Jazyk: angličtina
Rok vydání: 2021
Předmět:
0301 basic medicine
Polyamine
neuroblastoma
apoptosis
microRNA
mitochondria
reactive oxygen species
oncotherapy
chemistry.chemical_compound
0302 clinical medicine
Annexin
polyamine
Settore BIO/10 - Biochimica
Antineoplastic Combined Chemotherapy Protocols
Cytotoxic T cell
Settore BIO/06 - Anatomia Comparata E Citologia
Biology (General)
Membrane Potential
Mitochondrial

N-Myc Proto-Oncogene Protein
Chemistry
Caspase 3
General Medicine
Blot
Gene Expression Regulation
Neoplastic

030220 oncology & carcinogenesis
Amine Oxidase (Copper-Containing)
Signal Transduction
QH301-705.5
Article
NO
03 medical and health sciences
Neuroblastoma
Cell Line
Tumor

medicine
Animals
Humans
Propidium iodide
Rats
Wistar

Cell Proliferation
Oncogene
Gene Amplification
medicine.disease
Molecular biology
MicroRNAs
030104 developmental biology
Apoptosis
Spermine
Tumor Suppressor Protein p53
Zdroj: Cells, Vol 10, Iss 1950, p 1950 (2021)
Cells
Volume 10
Issue 8
Popis: Neuroblastoma (NB) is a common malignant solid tumor in children and accounts for 15% of childhood cancer mortality. Amplification of the N-Myc oncogene is a well-established poor prognostic marker in NB patients and strongly correlates with higher tumor aggression and resistance to treatment. New therapies for patients with N-Myc-amplified NB need to be developed. After treating NB cells with BSAO/SPM, the detection of apoptosis was determined after annexin V-FITC labeling and DNA staining with propidium iodide. The mitochondrial membrane potential activity was checked, labeling cells with the probe JC-1 dye. We analyzed, by real-time RT-PCR, the transcript of genes involved in the apoptotic process, to determine possible down- or upregulation of mRNAs after the treatment on SJNKP and the N-Myc-amplified IMR5 cell lines with BSAO/SPM. The experiments were carried out considering the proapoptotic genes Tp53 and caspase-3. After treatment with BSAO/SPM, both cell lines displayed increased mRNA levels for all these proapoptotic genes. Western blotting analysis with PARP and caspase-3 antibody support that BSAO/SPM treatment induces high levels of apoptosis in cells. The major conclusion is that BSAO/SPM treatment leads to antiproliferative and cytotoxic activity of both NB cell lines, associated with activation of apoptosis.
Databáze: OpenAIRE