Department of Biopharmaceutical Biotechnology, College of Life Science, Kyung Hee University, Yongin, 17104, Republic of Korea.
Department of Biotechnology and Genetic Engineering, Faculty of Biological Sciences, Islamic University, Kushtia, 7003, Bangladesh.
J Microbiol. 2024 Oct;62(10):919-927. doi: 10.1007/s12275-024-00163-8. Epub 2024 Oct 8.
In recent years, kidney cancer has become one of the most serious medical issues. Kidney cancer is treated with a variety of active compounds that trigger genes that cause cancer. We identified in our earlier research that isoquercitrin (IQ) can activate PIK3CA, IGF1R, and PTGS2. However, it has a very low bioavailability because of its lower solubility in water. So, we utilized sub-merge fermentation technology with two well-known probiotics, Lactobacillus acidophilus and Bacillus subtilis, as a microbial source and mulberry fruit extract as a substrate, which has a high IQ level to improve IQ yield. Furthermore, we compared the total phenolic, flavonoid, and antioxidant contents of fermented and non-fermented samples, and we found that the fermented samples had greater levels than non-fermented sample. In addition, the high-performance liquid chromatography (HPLC) results showed that the fermented mulberry fruit extract from B. subtilis and L. acidophilus showed higher IQ values (190.73 ± 0.004 μg/ml and 220.54 ± 0.007 μg/ml, respectively), compared to the non-fermented samples, which had IQ values (80.12 ± 0.002 μg/ml). Additionally, at 62.5 µg/ml doses of each sample, a normal kidney cell line (HEK 293) showed higher cell viability for fermented and non-fermented samples. Conversely, at the same doses, the fermented samples of L. acidophilus and B. subtilis in a kidney cancer cell line (A498) showed an inhibition of cell growth around 36% and 31%, respectively. Finally, we performed RT and qRT PCR assay, and we found a significant reduction in the expression of the PTGS2, PIK3CA, and IGF1R genes. We therefore can conclude that the fermented samples have a higher concentration of isoquercitrin, and also can inhibit the expression of the genes PTGS2, PIK3CA, and IGF1R, which in turn regulates kidney cancer and inflammation.
近年来,肾癌已成为最严重的医学问题之一。肾癌的治疗采用了多种能触发致癌基因的活性化合物。我们在早期研究中发现,异槲皮苷(IQ)可以激活 PIK3CA、IGF1R 和 PTGS2。然而,由于其在水中的溶解度较低,生物利用度非常低。因此,我们利用两种知名益生菌——嗜酸乳杆菌和枯草芽孢杆菌作为微生物源,以及桑椹果提取物作为底物,采用浸没式发酵技术,提高 IQ 的产量。此外,我们比较了发酵和未发酵样品的总酚、类黄酮和抗氧化含量,发现发酵样品的含量高于未发酵样品。此外,高效液相色谱(HPLC)结果表明,枯草芽孢杆菌和嗜酸乳杆菌发酵的桑椹果提取物中的 IQ 值较高(分别为 190.73 ± 0.004μg/ml 和 220.54 ± 0.007μg/ml),与未发酵样品(80.12 ± 0.002μg/ml)相比。此外,在 62.5μg/ml 剂量下,正常肾细胞系(HEK 293)对发酵和未发酵样品的细胞活力更高。相反,在相同剂量下,肾癌细胞系(A498)中发酵的嗜酸乳杆菌和枯草芽孢杆菌样品的细胞生长抑制率分别为 36%和 31%左右。最后,我们进行了 RT 和 qRT-PCR 检测,发现 PTGS2、PIK3CA 和 IGF1R 基因的表达显著降低。因此,我们可以得出结论,发酵样品中含有更高浓度的异槲皮苷,还可以抑制 PTGS2、PIK3CA 和 IGF1R 基因的表达,从而调节肾癌和炎症。