Title of article :
Antitumor Effects of Umbelliprenin in a Mouse Model of Colorectal Cancer
Author/Authors :
Naderi Alizadeh, Mohamad Department of Pharmacology - school of medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Rashidi, Mohsen Department of Physiology and Pharmacology - Faculty of Medicine - Mazandaran University of Medical Sciences, Sari, Iran , Muhammadnejad, Ahad Cancer Biology Research Center - Cancer Institute of Iran - Tehran University of Medical Sciences, Tehran, Iran , Moeini Zanjania, Taraneh Department of Pharmacology - school of medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Ziai, Ali Department of Pharmacology - school of medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Umbelliprenin is a sesquiterpene coumarin with vitro anti-carcinogenic activities. The aim
of this study was to investigate the antitumor effects of umbelliprenin in animal models of
colorectal cancer. The cytotoxic effects of umbelliprenin were explored on CT26 and L929by
MTT assay. In this study, colorectal tumors developed in mice by intradermal injection of
CT26 cell line. Tumor size, serum levels of IFN-γ and IL-4 by ELISA, and Ki-67, MMP2,
MMP9, VEGF and E-cadherin markers by IHC method were evaluated. The results showed that
umbelliprenin inhibited the cancer cells in a concentration-dependent manner. IC50 Evaluation
showed that L929 cells were more resistant to Umbelliprenin than CT26 cells. Umbelliprenin
treatment in both tumor-bearing mice and control normal mice showed significantly increased
IFN-γ and decreased IL-4(P < 0.05). The pathologic findings had shown that the E-cadherin
marker in the umbelliprenin treated cancerous mice were significantly higher compared to
the control group (P < 0.05) while the expression of Ki-67 marker was reduced significantly
(P < 0.05). Markers involved in angiogenesis including VEGF, MMP2, and MMP-9 in the
cancerous mice group treated with umbelliprenin showed a significant decrease compared to
the control group (P < 0.05). Metastasis to lung and liver was reduced in umbelliprenin treated
group. Our results showed that umbelliprenin inhibited CT26 tumor cells in-vitro. The in-vivo
reduction of tumor size, angiogenesis, and proliferation markers and the absence of metastasis
represents the antitumor effects of umbelliprenin on colorectal cancer. The results showed that
umbelliprenin can be considered as a good candidate for the treatment of colorectal cancer.
Keywords :
CT26, Anti-angiogenesis , Anti-carcinogenic effect , cytotoxic effect , Colorectal cancer , Umbelliprenin , Immunohistochemistry
Journal title :
Astroparticle Physics