The Hexane Fraction of Bursera microphylla A Gray Induces p21-Mediated Antiproliferative and Proapoptotic Effects in Human Cancer–Derived Cell Lines

Author:

Adorisio Sabrina1,Fierabracci Alessandra2,Gigliarelli Giulia3,Muscari Isabella4,Cannarile Lorenza1,Liberati Anna Marina4,Marcotullio Maria Carla3,Riccardi Carlo1,Curini Massimo3,Robles Zepeda Ramon Enrique5,Delfino Domenico V.16

Affiliation:

1. Section of Pharmacology, Department of Medicine, University of Perugia, Italy

2. Infectivology and Clinical Trials Area, Bambino Gesù Children’s Hospital IRCCS, Rome, Italy

3. Department of Pharmaceutical Sciences, University of Perugia, Italy

4. Section of Onco-hematology, S. Maria Terni Hospital, Department of Surgery and Medical Sciences, University of Perugia, Italy

5. Department of Chemical and Biological Science University of Sonora, Hermosillo, Mexico

6. Foligno Nursing School, Department of Medicine, University of Perugia, Italy

Abstract

Bursera microphylla (BM), one of the common elephant trees, is widely distributed in the Sonoran desert in Mexico. The Seri ethnic group in the Sonoran desert uses BM as an anti-inflammatory and painkiller drug for the treatment of sore throat, herpes labialis, abscessed tooth, and wound healing. Dried stems and leaves of BM are used in a tea to relieve painful urination and to stimulate bronchial secretion. Furthermore, BM is used for fighting venereal diseases. To investigate the effects of the hexane fraction of resin methanol extract (BM-H) on cell growth, the acute myeloid cell line (OCI-AML3) was treated with 250, 25, or 2.5 µg/mL of BM-H. The first 2 concentrations were able to significantly decrease OCI-AML3 cell number. This reduced cell number was associated with decreased S-phase, blockade of G2/M phase of the cell cycle, and increased cell death. Similar results were obtained on all tested tumor cell lines of different origins. We found that blockade of the cell cycle was a result of upregulation of p21 protein in a p53-independent way. Increase of p21 was possibly a result of upstream upregulation of p-ERK (which stabilizes p21 protein) and downregulation of p-38 (which promotes its degradation). Regarding cell death, activation of caspase-3, but not of caspase-8 or -9, was detectable after BM-H treatment. In conclusion, these data suggest that BM-H inhibited proliferation of cell lines mainly by a p21-dependent, p53-independent mechanism and promoted apoptosis through activation of caspase-3 but not caspase-8 or -9.

Publisher

SAGE Publications

Subject

Complementary and alternative medicine,Oncology

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