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Updated: Jan 22, 2026

Generation and Isolation of Cell Cycle-arrested Cells with Complex Karyotypes
Published on: April 13, 2018
Sonoran propolis induces a pro-apoptotic effect through mitotic arrest: a distinct cell cycle outcome compared with
Efrain Alday1, Patricia Ruiz-Bustos1, Adriana Garibay-Escobar1
1Department of Chemistry-Biology, University of Sonora, Blvd. Luis Encinas y Rosales s/n, Hermosillo, Sonora 83000, Mexico.
Objectives:
The aim of this study was to elucidate the molecular events of cell cycle progression underlying alterations in cell morphology, as well as the pro-apoptotic and antiproliferative effects of Sonoran propolis (SP) on cancer cells.
Methods:
Cell cycle progression was analysed in human (HeLa) and murine (M12.C3.F3) cancer cell lines treated with SP, its primarily plant source Populus fremontii resins (PFR), and other potential contributing plants [Bursera laxiflora, Ambrosia ambrosioides, and Ambrosia confertiflora (ACR)]. In addition, bio-guided fractionation was performed to identify potential minor bioactive phytochemicals involved and their botanical sources.
Key Findings:
SP (12.5 μg/ml) and ACR (3 μg/ml) induced mitotic arrest in both cancer cell models, characterized by an increase in elongated cyclin B1-positive cells, displaying alterations in nuclear and cytoskeleton organization, indicative of a defective spindle assembly checkpoint during metaphase. In contrast, PFR (12.5 μg/ml) increased cell population at G0/G1 in both cell lines, in comparison to dimethyl sulfoxide control. SP8020-XIV-7 chromatographic fraction induced G2/M arrest in treated cells, and Ultra-High Performance Liquid Chromatography-Quadrupole Time-Of-Flight Mass Spectrometry (UPLC-ESI-Q-TOF-HD-MS/MS) analysis revealed that it was composed by naringenin (<1%), kaempferol (23%), kaempferol-3-methyl ether (75%), and an unknown compound [(M-H)-: 343.0817 m/z, C18H16O7] (<2%), structurally related to eupatorin (G2/M inducer), which was additionally identified in ACR.
Conclusions:
We found that phytochemicals from A. confertiflora may contribute to SP bioactivity on cancer cells.
Insights
Sonoran propolis and Ambrosia confertiflora induce cell cycle arrest in cancer cells, impacting cell morphology and proliferation. Phytochemicals from Ambrosia confertiflora are key contributors to this bioactivity.
Area of Science:
- Phytochemistry
- Cell Biology
- Cancer Research
Background:
- Sonoran propolis (SP) exhibits antiproliferative and pro-apoptotic effects on cancer cells.
- Understanding the molecular mechanisms of SP's action is crucial for its therapeutic potential.
Purpose of the Study:
- To investigate the effects of Sonoran propolis (SP) on cancer cell cycle progression.
- To identify the specific phytochemicals responsible for SP's bioactivity.
Main Methods:
- Cell cycle analysis was performed on human (HeLa) and murine (M12.C3.F3) cancer cell lines.
- Bio-guided fractionation and UPLC-ESI-Q-TOF-HD-MS/MS were used to identify active compounds.
Main Results:
- SP and Ambrosia confertiflora (ACR) induced mitotic arrest, characterized by altered cell morphology and defective spindle assembly.
- Populus fremontii resins (PFR) increased the G0/G1 cell population.
- A fraction of SP (SP8020-XIV-7) induced G2/M arrest and contained kaempferol, kaempferol-3-methyl ether, and an unknown compound related to eupatorin.
Conclusions:
- Phytochemicals present in Ambrosia confertiflora (ACR) contribute significantly to the bioactivity of Sonoran propolis (SP).
- Specific compounds like kaempferol derivatives and eupatorin-related molecules may mediate cell cycle arrest.
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