The effect of Colchicum pusillum in human colon cancer cells via Wnt/β-catenin pathway.

Eda Becer, Duygu Yiğit Hanoğlu, Hilal Kabadayı, Azmi Hanoğlu, Seda Vatansever, Dudu Özkum Yavuz, Filiz Meriçli, Ali Hikmet Meriçli

Journal: Gene 2019;686():213-219

PMID: 30458290

Abstract

OBJECTIVE

Colchicum pusillum belongs to the family Colchicaceae that particularly rich in tropolonic alkaloids. The aim of this study was to investigate the cytotoxicity and in vitro anticancer activity of Colchicum pusillum ethanolic extract on Colo-320 primer and Colo-741 metastatic colon adenocarcinoma cell lines.

MATERIALS AND METHODS

Colchicum pusillum was collected and extracted with ethanol. Different concentrations of Colchicum pusillum extract were incubated for 24 h and 48 h with Colo-320 and Colo-741 cells. Cell growth and cytotoxicity were measured by 3‑(4,5‑dimethylthiazol‑2‑yl)‑2,5‑diphenyltetrazolium bromide (MTT) assays. Anticancer and antiproliferative activities of Colchicum pusillum were investigated by immunocytochemistry using antibodies directed against to β-catenin, Ki-67, LGR-5 Ki-67, DKK1, Frizzled-4, Wnt4, Wnt7a and caspase3 in Colo-741 cells.

RESULTS

All concentrations of Colchicum pusillum extract had toxic effect in Colo-320 cells. Because of this, we used Colchicum pusillum extract at 20 μg/ml for evaluate anticancer activities only in Colo-741 cells. As a result of immunohistochemical staining, β-catenin, LGR-5 and caspase-3 immunoreactivities were significantly increased while Wnt7a immunostaining intensity was decreased in Colo-741 cells. Conclusion We conclude that Colchicum pusillum extract increased β-catenin and LGR-5 via Wnt/β-catenin pathway in colon cancer cells. Interestingly, it decreased other signaling molecule, Wnt7a which is assumed to play protective role during carcinogenesis. Also, it increased significantly caspase-3 immunoreactivity showing that apoptotic pathways were triggered.

Copyright © 2018. Published by Elsevier B.V.

Address: Department of Biochemistry, Faculty of Pharmacy, Near East University, Nicosia, Cyprus; Experimental Health Research Center of Health Sciences, Near East University, Nicosia, Cyprus. Electronic address: [email protected].; Department of Pharmaceutical Botany, Faculty of Pharmacy, Near East University, Nicosia, Cyprus.; Department of Histology and Embryology, Faculty of Medicine, Celal Bayar University, Manisa, Turkey.; Experimental Health Research Center of Health Sciences, Near East University, Nicosia, Cyprus; Department of Histology and Embryology, Faculty of Medicine, Celal Bayar University, Manisa, Turkey.; Department of Pharmacognosy-Phytotherapy, Faculty of Pharmacy, Near East University, Nicosia, Cyprus.

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