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.
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Authors | Yue Han, Can Bai, Xi-Meng He, Qing-Ling Ren |
Journal | Purinergic signalling
(Purinergic Signal)
Vol. 19
Issue 1
Pg. 145-153
(03 2023)
ISSN: 1573-9546 [Electronic] Netherlands |
PMID | 35235139
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2022. The Author(s). |
Chemical References |
- atractylenolide I
- Purinergic P2X Receptor Antagonists
- Receptors, Purinergic P2X7
- Antineoplastic Agents
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Topics |
- Female
- Humans
- Cell Proliferation
- HeLa Cells
- Purinergic P2X Receptor Antagonists
(pharmacology)
- Receptors, Purinergic P2X7
- Uterine Cervical Neoplasms
- Antineoplastic Agents
(therapeutic use)
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