Back to Search Start Over

The α-Tomatine Exhibits Antiproliferative Activity, Rupture of Cell Membranes and Induces the Expression of APC Gene in the Human Colorectal Adenocarcinoma Cell Line (Ht-29)

Authors :
Priscila Lumi Ishii
Rodrigo Juliano Oliveira
Mariana de Oliveira Mauro
Verônica Assalin Zorgetto-Pinheiro
Daniele Sartori
Sandra Regina Lepri
Adrivanio Baranoski
Mário Sérgio Mantovani
Lúcia Regina Ribeiro
Source :
Brazilian Archives of Biology and Technology, Vol 63 (2020)
Publication Year :
2020
Publisher :
Instituto de Tecnologia do Paraná (Tecpar), 2020.

Abstract

Abstract The α-tomatine is a steroidal glycoalkaloid found in immature tomatoes (Lycopersicon esculentum) that has important biological functions including the inhibition of cancer cell growth and preventing metastasis. This study aimed to evaluate the effects of α-tomatine on cytotoxicity, cellular proliferation, apoptosis, and mRNA expression of APC, CCNA2, β-catenin, CASP9, BAK, BAX and BCL-XL in colorectal adenocarcinoma cell line HT-29. HT29 cells were treated with three concentrations of α-tomatine (0.1, 1 and 10 µg/mL), although only the 1 µg/mL concentration of α-tomatine was used to evaluate genetic expression patterns by real time-PCR. Results showed that α-tomatine was cytotoxic only at the 10 µg/mL concentration. Cell proliferation was significantly inhibited after the first 24 hours of treatment only with concentrations of 10 µg/mL. In contrast, there were no significant differences in apoptosis for any treatment. In the gene expression studies, only APC expression was significantly altered by α-tomatine treatment. In conclusion, α-tomatine has antiproliferative activity in the first 24h of treatment, does not induce apoptosis in this cell line and causes disruption of cell membranes, thereby increasing the expression of APC gene related to cell cycle.

Details

Language :
English
ISSN :
16784324
Volume :
63
Database :
Directory of Open Access Journals
Journal :
Brazilian Archives of Biology and Technology
Publication Type :
Academic Journal
Accession number :
edsdoj.41f24598501d43869480261888690d46
Document Type :
article
Full Text :
https://doi.org/10.1590/1678-4324-2020190395