P2X7 receptor involved in antitumor activity of atractylenolide I in human cervical cancer cells

Purinergic Signal. 2023 Mar;19(1):145-153. doi: 10.1007/s11302-022-09854-6. Epub 2022 Mar 2.

Abstract

Atractylenolide I (Atr-I) was found to sensitize a variety of human cancer cells in previous studies. Purinergic P2X7R plays important role in different cancers. However, whether Atr-I could generate antitumor activity in human cervical cancer cells and P2X7R get involved in this effect remain unclear. In this study, Hela (HPV 18 +) and SiHa (HPV 16 +) cells were treated with different doses of Atr-I. The results indicated that agonist and antagonist of P2X7 receptors, BzATP and JNJ-47965567 (JNJ), could suppress the proliferation of Hela and SiHa cells. Atr-I demonstrated a considerable antitumor effect in both human cervical cancer cells in vitro. Atr-I combined with P2X7R agonist, BzATP, restored Atr-I-induced growth inhibition in Hela cells but not in SiHa cells. However, the combinatorial treatment of P2X7R antagonist JNJ and Atr-I has an additive effect on cell growth inhibition in SiHa cells rather than in Hela cells. It implied that P2X7R would get involved in the anti-human cervical cancer cells effect of Atr-I.

Keywords: Atractylenolide I; Hela cells; Human cervical cancer cells; P2X7Rs; SiHa cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Cell Proliferation
  • Female
  • HeLa Cells
  • Humans
  • Purinergic P2X Receptor Antagonists / pharmacology
  • Receptors, Purinergic P2X7*
  • Uterine Cervical Neoplasms*

Substances

  • atractylenolide I
  • Purinergic P2X Receptor Antagonists
  • Receptors, Purinergic P2X7
  • Antineoplastic Agents