Goyal Shallu, Sharma Monika, Sharma Rohit
Department of Microbial Biotechnology, Panjab University, South Campus, Sector-25, Chandigarh, 160014 India.
Department of Biotechnology, Panjab University, South Campus, Sector-25, Chandigarh, 160014 India.
3 Biotech. 2022 Apr;12(4):96. doi: 10.1007/s13205-022-03155-w. Epub 2022 Mar 19.
The study was aimed at the identification of a potential anti-cancer compound from the leaf extract of , against pancreatic cancer cells (PANC-1). Out of different extracts tested, methanolic extract showed significant cytotoxicity at an IC of 289.5 ± 0.03 µg/mL after 24 h (MTT assay). The safety of the extract was ascertained using normal pancreatic cells (hTERT-HPNE). Methanolic extract was able to induce apoptosis in 28.9 ± 0.01% of PANC-1 cells as determined by flow cytometry. RT-PCR analysis of PANC-1 cells also recorded an increase in the mRNA expression of pro-apoptotic genes i.e., (12.82 folds), (10 folds) and (8.74 folds) after treatment. Expression of other pro-apoptotic genes such as and was also upregulated by 4.04 and 4.01 folds, respectively. However, the mRNA expression of anti-apoptotic genes, , and was found to be downregulated. The bioactive extract was then fractionated on preparative silica gel plates into 24 bands. Out of these, band fraction 9 exhibited significant cytotoxicity (IC 219 ± 0.04 µg/mL) on the PANC-1 cells. The mass spectral (HPLC-MS) and FTIR analysis of the fraction indicated the bioactive compound to be a derivative of Diosgenin, which can be a possible candidate for cancer therapeutics in future.
The online version contains supplementary material available at 10.1007/s13205-022-03155-w.
本研究旨在从[植物名称]叶提取物中鉴定一种潜在的抗癌化合物,用于对抗胰腺癌细胞(PANC-1)。在测试的不同提取物中,甲醇提取物在24小时后的IC50为289.5±0.03μg/mL时显示出显著的细胞毒性(MTT法)。使用正常胰腺细胞(hTERT-HPNE)确定了提取物的安全性。通过流式细胞术测定,甲醇提取物能够诱导28.9±0.01%的PANC-1细胞凋亡。对PANC-1细胞的RT-PCR分析还记录了处理后促凋亡基因即[基因名称1](12.82倍)、[基因名称2](10倍)和[基因名称3](8.74倍)的mRNA表达增加。其他促凋亡基因如[基因名称4]和[基因名称5]的表达也分别上调了4.04倍和4.01倍。然而,抗凋亡基因[基因名称6]、[基因名称7]和[基因名称8]的mRNA表达被发现下调。然后将生物活性提取物在制备型硅胶板上分离成24条带。其中,第9条带组分对PANC-1细胞表现出显著的细胞毒性(IC50为219±0.04μg/mL)。该组分的质谱(HPLC-MS)和FTIR分析表明生物活性化合物是薯蓣皂苷元的衍生物,未来可能是癌症治疗的候选药物。
在线版本包含可在10.1007/s13205-022-03155-w获取的补充材料。