Study on the Anti-tumor Activity of Components of Ganoderma Lucidum on the Three-dimensional Culture Model of Colorectal Cancer HCT116 Cells
10.13748/j.cnki.issn1007-7693.20222521
- VernacularTitle:基于结肠癌HCT116细胞三维培养模型的灵芝组分抗肿瘤活性研究
- Author:
PAN Haitao
1
,
2
;
CHEN Dongjie
1
,
2
;
ZHANG Guoliang
2
,
3
;
HU Lingjuan
3
;
WANG Xiaotong
3
,
4
;
ZHONG Yi
1
,
2
;
YANG Jihong
1
,
2
;
LI Zhenhao
1
,
2
,
3
Author Information
1. Zhejiang ShouXianGu Botanical Drug Institute Co., Ltd., Hangzhou 311100, China
2. Hangzhou Yuhang BoYu Intelligent Health Innovation Lab, Hangzhou 311100, China
3. Zhejiang ShouXianGu Pharmaceutical Co., Ltd., Wuyi 321200, China
4. Zhejiang Key Agricultural Enterprise Institute of ShouXianGu Rare Herb Products, Wuyi 321200, China
- Publication Type:Journal Article
- Keywords:
Ganoderma lucidum;
colorectal cancer;
three-dimensional culture;
lipolysis;
lipophagy
- From:
Chinese Journal of Modern Applied Pharmacy
2023;40(13):1795-1809
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE To investigate the anti-tumor effects of the components of Ganoderma lucidum(Gc) based on the two-dimensional(2D) and three-dimensional(3D) culture of colorectal cancer HCT116 cells. METHODS The chemical compositional of the three components was identified by UPLC-Q-TOF-MS. An in vitro 3D culture model of HCT116 cells was established by using Matrigel as the matrix material, and the effects of Gc1, Gc2, Gc3, and 5-fluorouracil(5-FU) on the proliferation of HCT116 cells in 2D and 3D culture models were evaluated, and the effects of Gc3 on cell-cycle, apoptosis, drug resistance, lipid metabolism, and 5-FU's anti-tumor activity were evaluated. Cell viability was detected by CCK-8 assay. mRNA expression level of the cells was analyzed by Real-time PCR. Proteins expression level of the cells was analyzed by Western blotting. HPLC was used to detect the content of 5-FU in cells. RESULTS A total of 76, 69, and 17 compounds were identified from Gc1, Gc2, and Gc3, respectively. Compared with 2D culture, the proliferation rate of HCT116 cells was decreased in the 3D culture model, and the expression of cell cycle-promoters CDK2, CDK4, CDK6, and fatty acid synthesizer FASN, SREBP1 were significantly down-regulated. On the contrary, the expression of cell cycle-suppressor p21, p27, and lipid droplet breakdown proteins ATGL and drug resistance gene ITGB1, CDH1, ABCB1, and ABCC1 mRNA were significantly up-regulated. Gc1, Gc2, Gc3 and 5-FU inhibited the proliferation of both 2D and 3D cultured HCT116 cells in a dose dependent manner after incubation for 48 h, and the inhibitory effect of Gc3 was significantly stronger than Gc1 and Gc2. Gc3 could not only reduce the expression of CDK2, CDK4, Bcl-xl, ATGL, and LC3B proteins, but also increase the expression of p21, p27, Bax, Cleaved caspase-3, and Cleaved PARP1 proteins, and overexpression of LC3B or ATGL attenuated Gc3-induced cytotoxicity in 3D cultured HCT116 cells. In addition, Gc3 significantly inhibited the expression of ITGB1, CDH1, ABCB1, and ABCC1 mRNA, and increased the intracellular 5-FU content, and enhanced the anti-tumor activity. CONCLUSION Gc3 significantly inhibit the proliferation of 3D-cultured HCT116 cells by inhibiting cell autophagy and lipid droplet breakdown, and enhance the anti-cancer activity of 5-FU by inhibiting the expression of ITGB1, CDH1, ABCB1, and ABCC1 mRNA.
