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Published on: September 30, 2016
Adiponectin Receptor Agonist Suppresses Human Colorectal Cancer
Mai Ly Thi Nguyen1, Lan Anh Bui2,3,4, Chi Pham2
1Department of Biochemistry, Military Hospital 103, Hanoi, Vietnam.
Background/Aim:
Colorectal cancer (CRC) was the third most commonly diagnosed cancer and the second leading cause of cancer-related deaths worldwide in 2022. Despite advances in oncology, CRC prognosis and treatment outcomes have shown limited improvement over the past decades, highlighting the urgent need for more effective therapies. Adiponectin signaling, known for its tumor-suppressive role in various cancers including CRC, presents a promising therapeutic target. AdipoRon, an adiponectin receptor agonist, may offer a novel strategy by restoring this signaling pathway.
Materials And Methods:
The anti-cancer effects of AdipoRon were evaluated in vitro using assays for cell viability, crystal violet staining, cell migration, apoptosis, and cell cycle distribution. Protein expression levels of AMPKα, phosphorylated AMPKα (pAMPKα), and STAT3 were assessed via western blotting.
Results:
AdipoRon significantly inhibited HCT116 colorectal cancer cell proliferation under both low and high-density conditions in a dose-dependent manner. It also reduced cell migration. Treated cells exhibited an increased tendency toward apoptosis and a significant accumulation in the G1 phase of the cell cycle, accompanied by reduced proportions in the S and G2/M phases. Furthermore, AdipoRon induced AMPKα phosphorylation and down-regulated the oncogenic protein STAT3.
Conclusion:
AdipoRon effectively inhibited CRC cell proliferation and migration in vitro, effects that were associated with the up-regulation of the tumor suppressor protein pAMPKα and suppression of STAT3. These findings support the potential of AdipoRon as a promising therapeutic agent for CRC.
Insights
AdipoRon, an adiponectin receptor agonist, inhibits colorectal cancer (CRC) cell growth and migration by activating tumor suppressor pathways. This study highlights AdipoRon
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Colorectal cancer (CRC) remains a leading cause of cancer deaths globally, with limited therapeutic advancements.
- Adiponectin signaling exhibits tumor-suppressive properties, making its pathway a potential therapeutic target for CRC.
- AdipoRon, an adiponectin receptor agonist, offers a novel strategy to restore adiponectin signaling.
Purpose of the Study:
- To investigate the anti-cancer effects of AdipoRon on colorectal cancer cells.
- To evaluate AdipoRon's impact on cell proliferation, migration, apoptosis, and cell cycle.
- To determine AdipoRon's effect on key signaling proteins like AMPKα and STAT3.
Main Methods:
- In vitro assays including cell viability, crystal violet staining, migration, apoptosis, and cell cycle analysis.
- Western blotting to assess protein expression levels of AMPKα, phosphorylated AMPKα (pAMPKα), and STAT3.
Main Results:
- AdipoRon significantly inhibited HCT116 CRC cell proliferation and migration in a dose-dependent manner.
- AdipoRon treatment led to increased apoptosis and G1 phase cell cycle arrest.
- AdipoRon induced AMPKα phosphorylation and decreased STAT3 expression.
Conclusions:
- AdipoRon demonstrates significant anti-cancer effects by inhibiting CRC cell proliferation and migration.
- These effects are mediated through the upregulation of pAMPKα and downregulation of STAT3.
- AdipoRon shows promise as a potential therapeutic agent for colorectal cancer.
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