AI Article Synopsis

  • Cancer chemotherapy often leads to toxicity and drug resistance, highlighting the need for better treatment options.
  • The study investigates the anti-leukemic effects of Withania somnifera root extract, focusing on its ability to induce immunogenic cell death (ICD) and its cytotoxic properties.
  • Findings indicate that the extract significantly kills cancer cells while inducing ICD, but also shows genotoxic effects, necessitating careful evaluation of its safety in various medical applications.

Article Abstract

Cancer chemotherapy is characterized by an elevated intrinsic toxicity and the development of drug resistance. Thus, there is a compelling need for new intervention strategies with an improved therapeutic profile. Immunogenic cell death (ICD) represents an innovative anticancer strategy where dying cancer cells release damage-associated molecular patterns promoting tumor-specific immune responses. The roots of Withania somnifera (W. somnifera) are used in the Indian traditional medicine for their anti-inflammatory, immunomodulating, neuroprotective, and anticancer activities. The present study is designed to explore the antileukemic activity of the dimethyl sulfoxide extract obtained from the roots of W. somnifera (WE). We studied its cytostatic and cytotoxic activity, its ability to induce ICD, and its genotoxic potential on a human T-lymphoblastoid cell line by using different flow cytometric assays. Our results show that WE has a significant cytotoxic and cytostatic potential, and induces ICD. Its proapoptotic mechanism involves intracellular Ca(2+) accumulation and the generation of reactive oxygen species. In our experimental conditions, the extract possesses a genotoxic potential. Since the use of Withania is suggested in different contexts including anti-infertility and osteoarthritis care, its genotoxicity should be carefully considered for an accurate assessment of its risk-benefit profile.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885062PMC
http://dx.doi.org/10.3390/toxins8050147DOI Listing

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