Marine drugs, 2023-04, Vol.21 (4), p.233
2023
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Details
- Autor(en) / Beteiligte
- Titel
- Marine Polyether Phycotoxin Palytoxin Induces Apoptotic Cell Death via Mcl-1 and Bcl-2 Downregulation
- Ist Teil von
- Marine drugs, 2023-04, Vol.21 (4), p.233
- Ort / Verlag
- Switzerland: MDPI AG
- Erscheinungsjahr
- 2023
- Quelle
- EZB-FREE-00999 freely available EZB journals
- Beschreibungen/Notizen
- Palytoxin is considered one of the most potent biotoxins. As palytoxin-induced cancer cell death mechanisms remain to be elucidated, we investigated this effect on various leukemia and solid tumor cell lines at low picomolar concentrations. As palytoxin did not affect the viability of peripheral blood mononuclear cells (PBMC) from healthy donors and did not create systemic toxicity in zebrafish, we confirmed excellent differential toxicity. Cell death was characterized by a multi-parametric approach involving the detection of nuclear condensation and caspase activation assays. zVAD-sensitive apoptotic cell death was concomitant with a dose-dependent downregulation of antiapoptotic Bcl-2 family proteins Mcl-1 and Bcl-xL. Proteasome inhibitor MG-132 prevented the proteolysis of Mcl-1, whereas the three major proteasomal enzymatic activities were upregulated by palytoxin. Palytoxin-induced dephosphorylation of Bcl-2 further exacerbated the proapoptotic effect of Mcl-1 and Bcl-xL degradation in a range of leukemia cell lines. As okadaic acid rescued cell death triggered by palytoxin, protein phosphatase (PP)2A was involved in Bcl-2 dephosphorylation and induction of apoptosis by palytoxin. At a translational level, palytoxin abrogated the colony formation capacity of leukemia cell types. Moreover, palytoxin abrogated tumor formation in a zebrafish xenograft assay at concentrations between 10 and 30 pM. Altogether, we provide evidence of the role of palytoxin as a very potent and promising anti-leukemic agent, acting at low picomolar concentrations in cellulo and in vivo.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 1660-3397eISSN: 1660-3397DOI: 10.3390/md21040233Titel-ID: cdi_doaj_primary_oai_doaj_org_article_dc0f952db529426c888e603cf53e66b2
- Format
- –
- Schlagworte
- Adenosine triphosphatase, Animals, Apoptosis, Apoptosis Regulatory Proteins - metabolism, Bcl-2, Bcl-2 protein, Bcl-x protein, bcl-X Protein - metabolism, bcl-X Protein - pharmacology, Biocompatibility, Cancer, Carbon, Caspase, Cell activation, Cell death, Cell Line, Tumor, Cell lines, Cells, Chemical properties, Colonies, Cytotoxicity, Danio rerio, Dephosphorylation, Down-Regulation, Drug therapy, Environmental Sciences, Enzymatic activity, Enzyme activity, Health aspects, Humans, Kinases, Leukemia, Leukocytes (mononuclear), Leukocytes, Mononuclear - metabolism, Lymphoma, Marine toxins, Mcl-1, Mcl-1 protein, Morphology, Mortality, Myeloid Cell Leukemia Sequence 1 Protein, Neoplasms, Okadaic acid, Palytoxin, Peripheral blood mononuclear cells, Phosphatase, Phosphorylation, Physiological aspects, Proteasome inhibitors, Proteasomes, Protein phosphatase, Proteins, Proteolysis, Proto-Oncogene Proteins c-bcl-2 - metabolism, Solid tumors, Toxicity, Toxins, Tumor cell lines, Tumors, Xenotransplantation, Zebrafish, Zebrafish - metabolism