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Updated: Sep 26, 2026

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols
Published on: June 6, 2017
[Effects of microcystins on cell cycle and expressions of c-fos and c-jun]
1School of Public Health, Fudan University, Shanghai 200032, China.
Objectives:
To investigate the effects of microcystins on cell cycle and expressions of c-fos and c-jun, and explore the potential carcinogenic mechanisms of Microcystins.
Methods:
Microcystic cyanobacteria extraction (MCE) purified by Sep-Pak C(18) cartridge was added into the media and co-incubated with SHE cell for various periods. Immunohistochemistry assay was applied to detect the expressions of c-fos and c-jun at 1, 3, 6 hr time point, and cell cycle at 6, 12, 24 hr point were analyzed by flow cytometry respectively.
Results:
Sustained up-regulated expression of c-fos and c-jun were induced by MCE during the experimental period, and 5 - 6 folds increased expression were observed at 6 hour point after treatment. As much as 44.8 per cent of cells were induced to entry S-phase from resting G(0)/G(1).
Conclusion:
Up-regulating the expression of transcript factor such as c-fos and c-jun thus to induce cell abnormal proliferation may be the potential carcinogenic mechanisms of microcystins.
Insights
Microcystins exposure up-regulates c-fos and c-jun expression, driving abnormal cell proliferation. This suggests a potential carcinogenic mechanism for microcystins, impacting cell cycle progression.
Area of Science:
- Environmental toxicology
- Cellular biology
- Molecular carcinogenesis
Context:
- Microcystins are potent toxins produced by cyanobacteria.
- Exposure to microcystins poses a significant risk to aquatic ecosystems and human health.
- Understanding the molecular mechanisms of microcystin toxicity is crucial for risk assessment.
Purpose:
- To investigate the effects of microcystins on cell cycle regulation.
- To examine the impact of microcystins on the expression of c-fos and c-jun proto-oncogenes.
- To elucidate the potential carcinogenic pathways initiated by microcystins.
Summary:
- Microcystins induced sustained up-regulation of c-fos and c-jun expression in SHE cells, with a 5-6 fold increase observed at 6 hours.
- A significant portion of cells (44.8%) were stimulated to enter the S-phase from the G(0)/G(1) resting phase.
- These findings indicate that microcystins can disrupt normal cell cycle progression and promote cellular proliferation.
Impact:
- This study reveals a potential carcinogenic mechanism for microcystins involving the induction of transcription factors like c-fos and c-jun.
- The findings contribute to a better understanding of microcystin-induced cellular damage and cancer risk.
- This research has implications for public health policies and environmental monitoring related to cyanobacterial blooms.
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