AdipoRon, Adiponectin Receptor Agonist, Exhibits Antiproliferative and Apoptotic Effects in HT29 and HCT116 Colon Cancer Cells

AdipoRon is the first synthetic analog of endogenous adiponectin, which is an adipose tissue derived hormone. As it is characterized with pharmacological properties like adiponectin through binding and activating AdipoR1 and AdipoR2 receptors this makes it a target for therapeutic treatments for a multitude of disorders. In this study AdipoRon effect on HT29 and HCT116 colon cancer cells were investigated. Cytotoxic activity of AdipoRon was observed, with a significant inhibition rate in HT29 and HCT116 cells. Moreover, there was a significant decrease in the number of HCT116 colonies by clonogenicity test. In addition, cell migration assay showed significant decrease in cell migration especially after 24 hours after treatment and more with 24 μM concentration of Adiporon. Immunofluorescence staining showed an increase of apoptotic caspase 3 and decrease of anti-apoptotic Bcl-2 in HCT11 in cells incubated with AdipoRon (6 μM) for 24 hours. Western blotting demonstrated a decrease in cell number with AdipoRon treatment, cyclin D1 was also suppressed. In addition, treatment with AdipoRon increases the phosphorylation of P27 as well as p AKT. In conclusion, our findings provide initial evidence of AdipoRon as an anticancer activity towards colon cancer cells; therefore, encouraging and designing future studies to further understand this pattern is essential. Keywords: AdipoRon, cytotoxicity, apoptotic, colon cancer cells, antiproliferative

Authors

Publication Details

Journal
Saudi Toxicology Journal
Published
2025-03-14
DOI
https://doi.org/10.70957/uqu.edu.sa/s.toxicology.s/stj.2025.2.1
Primary Topic
Cancer, Lipids, and Metabolism
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

AdipoRon, Adiponectin Receptor Agonist, Exhibits Antiproliferative and Apoptotic Effects in HT29 and HCT116 Colon Cancer Cells

Alanood S. Algarni, Ashraf N. Abdalla, Yosra Zakariyya Alhindi, Mohamed Elzubier et al.
Saudi Toxicology Journal
Cancer, Lipids, and Metabolism
article

AdipoRon, Adiponectin Receptor Agonist, Exhibits Antiproliferative and Apoptotic Effects in HT29 and HCT116 Colon Cancer Cells

Alanood S. Algarni, Ashraf N. Abdalla, Yosra Zakariyya Alhindi, Mohamed Elzubier, Riyad A. Almaimani, Amin A. Hafiz, Arwa Fairaq, Halah A. Hafiz
article en

Abstract

AdipoRon is the first synthetic analog of endogenous adiponectin, which is an adipose tissue derived hormone. As it is characterized with pharmacological properties like adiponectin through binding and activating AdipoR1 and AdipoR2 receptors this makes it a target for therapeutic treatments for a multitude of disorders. In this study AdipoRon effect on HT29 and HCT116 colon cancer cells were investigated. Cytotoxic activity of AdipoRon was observed, with a significant inhibition rate in HT29 and HCT116 cells. Moreover, there was a significant decrease in the number of HCT116 colonies by clonogenicity test. In addition, cell migration assay showed significant decrease in cell migration especially after 24 hours after treatment and more with 24 μM concentration of Adiporon. Immunofluorescence staining showed an increase of apoptotic caspase 3 and decrease of anti-apoptotic Bcl-2 in HCT11 in cells incubated with AdipoRon (6 μM) for 24 hours. Western blotting demonstrated a decrease in cell number with AdipoRon treatment, cyclin D1 was also suppressed. In addition, treatment with AdipoRon increases the phosphorylation of P27 as well as p AKT. In conclusion, our findings provide initial evidence of AdipoRon as an anticancer activity towards colon cancer cells; therefore, encouraging and designing future studies to further understand this pattern is essential. Keywords: AdipoRon, cytotoxicity, apoptotic, colon cancer cells, antiproliferative

Saudi Toxicology Journal
Good health and well-being
Openalex Percentile: Top 94%
Cancer, Lipids, and Metabolism
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.