Curcumin aggravates the mitochondria damages of colon cancer cell line HCT-116 and promotes the apoptosis of the cells

Xu Mingliang, Kang Qingmei, Zhang Shuntao, Zhang Xiong, Gao Minna, Zeng Bo

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Journal of Chongqing Medical University ›› 2024, Vol. 49 ›› Issue (03) : 270-275. DOI: 10.13406/j.cnki.cyxb.003451
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Curcumin aggravates the mitochondria damages of colon cancer cell line HCT-116 and promotes the apoptosis of the cells

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Abstract

Objective To observe the effects of curcumin on the proliferation and apoptosis of colon cancer cell line HCT-116 as well as on the changes in mitochondrial morphology and function,and to explore the potential mechanism. Methods Colon cancer cell line HCT-116 was cultured in vitro and treated with different concentrations of curcumin(5,10,20,and 30 μmol/L). Cell count kit-8 was used to observe the changes in cell proliferation,and the optimal concentration was identified. Flow cytometry was used for determination of the changes in cell apoptosis. Mitochondrial membrane potential assay kit JC-1 was applied to determine the changes in intracellular mitochondrial membrane potential. Electron microscopy and Mito Tracker Deep Red staining were used for observing the changes in mitochondrial morphology and structure. The changes in cellular adenosine triphosphate(ATP) and reactive oxygen species(ROS) were assessed by the corresponding assay kits. The changes in the activities and protein levels of apoptosis-related caspase-3 and caspase-9 enzymes were measured by spectrophotometry and western blotting,respectively. Results After curcumin treatment,the proliferation of HCT-116 cells was significantly inhibited in a concentration-time dependent manner,and the half maximal inhibitory concentration was 13 μmol/L. Curcumin not only remarkably increased the proportion of cells in early apoptosis,but also significantly reduced the intracellular mitochondrial membrane potential level in a concentration dependent manner. The electron microscopy results showed that curcumin caused obvious mitochondrial swelling in cells,including crista swelling,disappearance,membrane rupture,and vacuoles. Mito Tracker Deep Red staining showed a significant decrease in mitochondria number and fragmentation appearance. The intracellular ATP production was significantly decreased. In addition,curcumin also increased the activities and protein expression of caspase-3 and caspase-9 enzymes in cells. Conclusion Curcumin inhibits the proliferation of colon cancer HCT-116 cells and promotes cell apoptosis. The mechanism is related to the aggravation of mitochondrial morphology and function damage by curcumin.

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cell line HCT-116 / curcumin / apoptosis / mitochondria

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Xu Mingliang , Kang Qingmei , Zhang Shuntao , et al . Curcumin aggravates the mitochondria damages of colon cancer cell line HCT-116 and promotes the apoptosis of the cells. Journal of Chongqing Medical University. 2024, 49(03): 270-275 https://doi.org/10.13406/j.cnki.cyxb.003451

References

1
Dilly A Honick BD Lee YJ,et al. Rational application of targeted therapeutics in mucinous colon/appendix cancers with positive predictive factors[J]. Cancer Med20209(5):1753-1767.
2
Wang ZH Chen L Li W,et al. Mitochondria transfer and transplantation in human health and diseases[J]. Mitochondrion202265:80-87.
3
Zhang L Zhang W Li ZY,et al. Mitochondria dysfunction in CD8+ T cells as an important contributing factor for cancer development and a potential target for cancer treatment:a review[J]. J Exp Clin Cancer Res202241(1):227.
4
She G Du JC Wu W,et al. Hippo pathway activation mediates chemotherapy-induced anti-cancer effect and cardiomyopathy through causing mitochondrial damage and dysfunction[J]. Theranostics202313(2):560-577.
5
Justo MP Cardoso CBM Cantiga-Silva C,et al. Curcumin reduces inflammation in rat apical periodontitis[J]. Int Endod J202255(11):1241-1251.
6
Hussain H Ahmad S Shah SWA,et al. Synthetic mono-carbonyl curcumin analogues attenuate oxidative stress in mouse models[J]. Biomedicines202210(10):2597.
7
Bland AR Ashton JC Kamal MA,et al. The current evidence for the therapeutic role of curcumin in Alzheimer’s disease[J]. CNS Neurol Disord Drug Targets202322(3):318-320.
8
Almoshari Y Iqbal H Razzaq A,et al. Development of nanocubosomes co-loaded with dual anticancer agents curcumin and temozolomide for effective Colon cancer therapy[J]. Drug Deliv202229(1):2633-2643.
9
Shelash Al-Hawary SI Abdalkareem Jasim S Kadhim M M,et al. Curcumin in the treatment of liver cancer:from mechanisms of action to nanoformulations[J]. Phytother Res202337(4):1624-1639.
10
He W Xia YQ Cao PH,et al. Curcuminoid WZ35 synergize with cisplatin by inducing ROS production and inhibiting TrxR1 activity in gastric cancer cells[J]. J Exp Clin Cancer Res201938(1):207.
11
Karthika C Sureshkumar R Sajini DV,et al. 5-fluorouracil and curcumin with pectin coating as a treatment regimen for titanium dioxide with dimethylhydrazine-induced colon cancer model[J]. Environ Sci Pollut Res Int202229(42):63202-63215.
12
Selvam C Prabu SL Jordan BC,et al. Molecular mechanisms of curcumin and its analogs in colon cancer prevention and treatment[J]. Life Sci2019239:117032.
13
Li H Yan LP Tang EKY,et al. Synthesis of TPGS/curcumin nanoparticles by thin-film hydration and evaluation of their anti-colon cancer efficacy in vitro and in vivo [J]. Front Pharmacol201910:769.
14
Hanahan D Weinberg RA. Hallmarks of cancer:the next generation[J]. Cell2011144(5):646-674.
15
Kotha RR Luthria DL. Curcumin:biological,pharmaceutical,nutraceutical,and analytical aspects[J]. Molecules201924(16):2930.
16
Chou YT Koh YC Nagabhushanam K,et al. A natural degradant of curcumin,feruloylacetone inhibits cell proliferation via inducing cell cycle arrest and a mitochondrial apoptotic pathway in HCT116 colon cancer cells[J]. Molecules202126(16):4884.
17
Xiang L He B Liu Q,et al. Antitumor effects of curcumin on the proliferation,migration and apoptosis of human colorectal carcinoma HCT-116 cells[J]. Oncol Rep202044(5):1997-2008.

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