The Anticancer Activity of Chalcone Compounds against Human Prostate Carcinoma Cell And Human Colon Colorectal Adenocarcinoma

Bedriye Seda Kurşun Aktar, A. S. Yaglıoglu, E. E. Oruç-Emre
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Abstract

Cancer is the second most common cause of death in our country and also worldwide. In the cancer treatment are used many methods such as surgery, chemotherapy, radiotherapy and hormone therapy. Despite these methods, a decrease is not observed in cancer cases and in the mortality. In addition, cancer drugs cause serious side effects. Therefore, there is a need for new anticancer drugs. Chalcones have broad anticancer activity against various cancer cells. In this study, the anticancer activities of the chalcone compounds were investigated against PC3 (Human Prostate Carcinoma Cell) and HT29 (Human colon colorectal adenocarcinoma) cell lines. The anticancer activity tests were performed using the BrdU ELISA method. 5 - Fluorouracil (5 - FU) was used as the positive control. Compound 1-7 ( except Compound 3 ) were determined having higher anticancer activity than 5 - FU against PC3 cancer cells. IC 50 values of the compounds 1-7 against PC3 cancer cells were 2.53±0.02 µM ; 4.40±0.03 µM ; 5.86±0.02 µM ; 4.36±0.03 µM; 1.76±0.02 µM ; 1.78±0.03 µM ; 2.31±0.03 µM , respectively.
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查尔酮类化合物对人前列腺癌细胞和人大肠癌的抗癌作用
癌症是我国乃至全世界第二大常见死因。在癌症治疗中使用了许多方法,如手术、化疗、放疗和激素治疗。尽管采用了这些方法,癌症病例和死亡率并未出现下降。此外,抗癌药物会产生严重的副作用。因此,有必要开发新的抗癌药物。查尔酮对多种癌细胞具有广泛的抗癌活性。本实验研究了查尔酮类化合物对人前列腺癌细胞(PC3)和人结肠直肠腺癌细胞(HT29)的抑癌活性。采用BrdU酶联免疫吸附试验进行抗肿瘤活性试验。5 -氟尿嘧啶(5 - FU)作为阳性对照。化合物1-7(除化合物3外)对PC3癌细胞的抗癌活性高于5 - FU。化合物1 ~ 7对PC3癌细胞的ic50值为2.53±0.02µM;4.40±0.03µm;5.86±0.02µm;4.36±0.03µM;1.76±0.02µm;1.78±0.03µm;分别为2.31±0.03µM。
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