Gholizadeh Siahmazgi Zohreh, Irani Shiva, Ghiaseddin Ali, Fallah Parviz, Haghpanah Vahid
Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Department of Biomedical Engineering Division, Chemical Engineering Faculty, Tarbiat Modares University, Tehran, Iran.
Cancer Cell Int. 2023 Aug 2;23(1):153. doi: 10.1186/s12935-023-03009-2.
Despite recent advances in the treatment of lung and breast cancer, the mortality with these two types of cancer is high. Xanthohumol (XN) is known as a bioactive compound that shows an anticancer effect on cancer cells. Here, we intended to investigate the anticancer effects of XN on the breast and lung cancer cell lines, using the three-dimensional (3D) cell culture.
XN was isolated from Humulus lupulus using Preparative-Thin Layer Chromatography (P-TLC) method and its authenticity was documented through Fourier Transform Infrared spectroscopy (FT-IR) and Hydrogen Nuclear Magnetic Resonance (H-NMR) methods. The spheroids of the breast (MCF-7) and lung (A549) cancer cell lines were prepared by the Hanging Drop (HD) method. Subsequently, the IC of XN were determined using the MTT assay in 2D and 3D cultures. Apoptosis was evaluated by Annexin V/PI flow cytometry and NFκB1/2, BAX, BCL2, and SURVIVIN expressions. Cell cycle progression was determined by P21, and P53 expressions as well as PI flow cytometry assays. Multidrug resistance was investigated through examining the expression of MDR1 and ABCG2. The invasion was examined by MMP2, MMP9, and FAK expression and F-actin labeling with Phalloidin-iFluor.
While the IC for the XN treatment were 1.9 µM and 4.74 µM in 2D cultures, these values were 12.37 µM and 31.17 µM in 3D cultures of MCF-7 and A549 cells, respectively. XN induced apoptosis in MCF-7 and A549 cell lines. Furthermore, XN treatment reduced cell cycle progression, multidrug resistance, and invasion at the molecular and/or cellular levels.
According to our results of XN treatment in 3D conditions, this bioactive compound can be introduced as an adjuvant anti-cancer agent for breast and lung cancer.
尽管肺癌和乳腺癌的治疗最近取得了进展,但这两种癌症的死亡率仍然很高。黄腐酚(XN)是一种具有生物活性的化合物,对癌细胞具有抗癌作用。在此,我们旨在使用三维(3D)细胞培养研究XN对乳腺癌和肺癌细胞系的抗癌作用。
采用制备型薄层色谱法(P-TLC)从啤酒花中分离出XN,并通过傅里叶变换红外光谱法(FT-IR)和氢核磁共振法(H-NMR)对其真实性进行了记录。采用悬滴法(HD)制备乳腺癌(MCF-7)和肺癌(A549)细胞系的球体。随后,在二维和三维培养中使用MTT法测定XN的半数抑制浓度(IC)。通过膜联蛋白V/碘化丙啶流式细胞术以及NFκB1/2、BAX、BCL2和存活素(SURVIVIN)的表达评估细胞凋亡。通过P21、P53的表达以及碘化丙啶流式细胞术测定细胞周期进程。通过检测多药耐药蛋白1(MDR1)和ATP结合盒转运蛋白G2(ABCG2)的表达来研究多药耐药性。通过基质金属蛋白酶2(MMP2)、基质金属蛋白酶9(MMP9)和粘着斑激酶(FAK)的表达以及用鬼笔环肽-iFluor对F-肌动蛋白进行标记来检测细胞侵袭。
在二维培养中,XN处理的半数抑制浓度分别为1.9 μM和4.74 μM;而在MCF-7和A549细胞的三维培养中,这些值分别为12.37 μM和31.17 μM。XN诱导MCF-7和A549细胞系凋亡。此外,XN处理在分子和/或细胞水平上降低了细胞周期进程、多药耐药性和细胞侵袭。
根据我们在三维条件下对XN处理的结果,可以将这种生物活性化合物作为乳腺癌和肺癌的辅助抗癌剂。