Title of article :
The anticancer activity of (e)-1-(4’-aminophenyl)-3-phenylprop-2-en-1-on against DMBA-induced mammary cancer in Sprague Dawley rat through the regulation of microRNA-21 expression
Author/Authors :
wahyuniari, ida ayu ika udayana university - faculty of medicine - department of histology, Indonesia , arijana, i g k nyoman udayana university - faculty of medicine - department of histology, Indonesia , sriwidyani, ni putu udayana university - faculty of medicine - department of anatomical pathology, Indonesia , wiryanthini, ida ayu dewi udayana university - faculty of medicine - department of biochemistry, Indonesia , suwito, hery universitas airlangga - faculty of science and technology - department of chemistry, Indonesia , widyarini, sitarina universitas gadjah mada - faculty of veterinary science - department of anatomical pathology, indonesia , ghufron, muhammad universitas gadjah mada - faculty of medicine - department of histology and cell biology, Indonesia , mustofa, . universitas gadjah mada - faculty of medicine - department of pharmacology and therapy, INDONESIA , mubarika, sofia universitas gadjah mada - faculty of medicine - department of histology and cell biology, Indonesia
Abstract :
Background: The new anticancer is urgently needed due to the high resistance and recurrence of breast cancer. The previous study reported that a new chalcone derivative, (e)-1-(4’-aminophenyl)-3-phenylprop-2-en-1-on, has a potential cytotoxicity against T47D breast cancer cell line. In this study we investigated the anticancer activity of (e)-1-(4’-aminophenyl)-3-phenylprop-2-en-1-on against DMBA-induced mammary cancer in Sprague-Dawley rat and its effect on microRNA-21 expression. Methods: Twenty-four female rats were divided into six groups. The first group, G1 received corn oil. The groups 2 to 6 (G2, G3, T1, T2, and T3) were induced by DMBA (dissolved in corn oil) 20 mg/kgBW for five weeks. After breast nodule had observed, G2 received the vehicle, and G3 received tamoxifen. Whereas, T1, T2, T3 received (e)-1-(4’-aminophenyl)-3-phenylprop-2-en-1-on with different doses, ie. 5, 15, and 45 mg/kgBW/day for 21 days, respectively. Tumor size was measured every week for 21 days, and on day 22, plasma and breast tissues were collected to examine the miR-21 expression by qRT-PCR and histopathological feature, respectively. Result: The result showed that significantly decreased tumor growth (p 0.05) and better histopathological malignant grading in G3, T1, T2, T3 were observed. Moreover, significantly reduced miR-21 relative expression (p 0.05) in G3, T1, and T2 were also observed. Conclusion: (e)-1-(4’-aminophenyl)-3-phenylprop-2-en-1-on has potential anticancer activity on DMBA-induced mammary cancer in Sprague-Dawley rat through its activity on miR-21 expression. Hence, (e)-1-(4’-aminophenyl)-3-phenylprop-2-en-1-on might be a new anticancer candidate in the future.
Keywords :
(e) , 1 , (4’ , aminophenyl) , 3 , phenylprop , 2 , en , 1 , on , tumor growth , histopathology , micro RNA , 21 expression , breast cancer
Journal title :
Bali Medical Journal (BMJ)
Journal title :
Bali Medical Journal (BMJ)