4.7 Article

Molecular characterization of the anticancer properties associated with bee venom and its components in glioblastoma multiforme

Journal

CHEMICO-BIOLOGICAL INTERACTIONS
Volume 347, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.cbi.2021.109622

Keywords

Brain tumor; Glioma; Cancer; Apitoxin; Apoptosis; Non-coding RNAs

Funding

  1. Canadian Institutes of Health Research
  2. New Brunswick Health Research Foundation
  3. New Brunswick Innovation Foundation
  4. DUO2018 initiative
  5. Universite de Moncton

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Glioblastoma multiforme (GBM) is a common form of malignant glioma with limited treatment options, highlighting the importance of developing new therapeutic approaches. This study found that bee venom and its components exhibit anti-cancer activities in human glioma cells by impacting apoptosis, necrosis, and the expression levels of certain genes, suggesting potential value in the treatment of GBM.
Glioblastoma multiforme (GBM) is a frequent form of malignant glioma. Strategic therapeutic approaches to treat this type of brain tumor currently involves a combination of surgery, radiotherapy and chemotherapy. Nevertheless, survival of GBM patients remains in the 12-15 months range following diagnosis. Development of novel therapeutic approaches for this malignancy is therefore of utmost importance. Interestingly, bee venom and its components have shown promising anti-cancer activities in various types of cancer even though information pertaining to GBMs have been limited. The current work was thus undertaken to better characterize the anticancer properties of bee venom and its components in Hs683, T98G and U373 human glioma cells. MTTbased cell viability assays revealed IC50 values of 7.12, 15.35 and 7.60 mu g/mL for cell lines Hs683, T98G and U373 treated with bee venom, respectively. Furthermore, melittin treatment of these cell lines resulted in IC50 values of 7.77, 31.53 and 12.34 mu g/mL, respectively. Cell viability assessment by flow cytometry analysis confirmed signs of late apoptosis and necrosis after only 1 h of treatment with either bee venom or melittin in all three cell lines. Immunoblotting-based quantification of apoptotic markers demonstrated increased expression of Bak and Bax, while Caspsase-3 levels were significantly lower when compared to control cells. Quantification by qRT-PCR showed increased expression levels of long non-coding RNAs RP11-838N2.4 and XIST in glioma cells treated with either bee venom or melittin. Overall, this study provides preliminary insight on molecular mechanisms via which bee venom and its main components can impact viability of glioma cells and warrants further investigation of its anticancer potential in gliomas.

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