A phytotherapic blend immunity-6™ inhibits myeloid leukemic cells 2 activation involving purinergic signaling

Biomed Pharmacother. 2023 Mar:159:114263. doi: 10.1016/j.biopha.2023.114263. Epub 2023 Jan 16.

Abstract

Leukemia is among the most common types of hematological cancers and the use of herbal medicines to prevent and treat leukemia are under quick development. Among several molecular pathways involved in leukemia pathogenesis and exacerbations, purinergic signaling is revealed as a key component. In the present study, the effects of two doses (5 ug/mL and 10 ug/mL) of Immunity-6™, a phytocomplex composed by beta-glucan, green tea (Camelia sinensis), chamomile (Matricaria chamomilla), and ascorbic acid (vitamin C) was tested in vitro, using chronic myelogenous leukemia cell line (K-562; 5 ×104/mL/well), which were challenged with lipopolysaccharide (LPS; 1 ug/mL) for 24 h. The results demonstrated that both doses of Immunity-6™ inhibited ATP release (p < 0.001) and P2×7 receptor at mRNA levels expression (p < 0.001). Purinergic inhibition by Immunity-6™ was followed by reduced release of proinflammatory cytokines IL-1beta (p < 0.001) and IL-6 (p < 0.001), while only 5 ug/mL of Immunity-6™ reduced the release of TNF-alpha (p < 0.001). Beyond to inhibit the release of pro-inflammatory cytokines, both doses of Immunity-6™ induced the release of anti-inflammatory cytokine IL-10 (p < 0.001), while only the higher dose (10 ug/mL) of Immunity-6™ induced the release of anti-inflammatory IL-1ra (p < 0.05) and klotho (p < 0.001). Thus, Immunity-6™ may be a promising adjuvant in the treatment of leukemia and further clinical trials are guaranteed.

Keywords: ATP; Cancer; Cytokines; Leukemia; Purinergic signaling.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Cell Line, Tumor
  • Cytokines* / metabolism
  • Humans
  • Interleukin-1beta / metabolism
  • Leukemia* / drug therapy
  • Lipopolysaccharides / pharmacology
  • Phytotherapy*
  • Receptors, Purinergic P2X7 / metabolism
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Adenosine Triphosphate
  • Cytokines
  • Interleukin-1beta
  • Lipopolysaccharides
  • Receptors, Purinergic P2X7
  • Tumor Necrosis Factor-alpha