TY - JOUR ID - 29516 TI - Induction of AHR Gene Expression in Colorectal Cancer Cell Lines by Cucurbitacin D, E, and I JO - Journal of Cell and Molecular Research JA - JCMR LA - en SN - 2008-9147 AU - Aftabi, Younes AU - Zarredar, Habib AU - Sheikhi, Mohammadreza AU - Khoshkam, Zahra AU - Hosseinzadeh Colagar, Abasalt AD - Tabriz University of Medical Sciences; University of Mazandaran, Babolsar, Mazandaran AD - Tabriz University of Medical Sciences, Tabriz, Iran AD - University of Tehran, Tehran, Iran AD - University of Mazandaran, Babolsar, Mazandaran, Iran Y1 - 2019 PY - 2019 VL - 10 IS - 2 SP - 67 EP - 75 KW - Aryl hydrocarbon receptor KW - Colon cancer KW - Cucurbitacin KW - HT-29 KW - SW-480 DO - 10.22067/jcmr.v10i2.74806 N2 -      Aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor and its induction may result in suppressing of cell proliferation in colorectal cancer (CRC). Cucurbitacin D (CucD), E (CucE) and I (CucI) are plant derived metabolites that inhibit cancer cells. This study aimed to evaluate the possible potency of the cucurbitacins for activation of AHR expression in CRC cell lines SW-480 and HT-29. The MTT assay was used to find the LC50 value of the metabolites in the cell lines. Afterward, the cells incubated with the LC50 concentrations and AHR-mRNA expression assessed using RT-PCR. The LC50 values of CucD, CucE, and CucI were 4.5, 6.8, and 3.8 μM in HT-29 cell line and 35, 19, 17.5 μM in SW-480 cells respectively. The SW-480 cells were more resistant against Cucs in comparison with HT-29 cells and all three Cucs cause to more AHR-mRNA expression in HT-29 cells. CucE had the lowest effect on AHR-mRNA expression in the cell lines and CucI was a common metabolite for both HT-29 and SW-480 cells, which showed the lowest LC50 value (the highest toxicity) and the highest effect on AHR-mRNA expression. CucI may have a potential to be used as an activator of AHR expression in CRC studies. UR - https://jcmr.um.ac.ir/article_29516.html L1 - https://jcmr.um.ac.ir/article_29516_e06ad1773f35704adab1b9e8d4865167.pdf ER -