Hydrangea serrata extract exerts tumor inhibitory activity against hepatocellular carcinoma HepG2 cells via inducing p27/CDK2-mediated cell cycle arrest and apoptosis

Ye-eun Kim , Jeonghye Hwang , Ki-Young Kim

Asian Pacific Journal of Tropical Biomedicine ›› 2024, Vol. 14 ›› Issue (2) : 65 -72.

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Asian Pacific Journal of Tropical Biomedicine ›› 2024, Vol. 14 ›› Issue (2) :65 -72. DOI: 10.4103/apjtb.apjtb_783_23
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Hydrangea serrata extract exerts tumor inhibitory activity against hepatocellular carcinoma HepG2 cells via inducing p27/CDK2-mediated cell cycle arrest and apoptosis
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Abstract

Objective: To examine the inhibitory effect of Hydrangea serrata extract against hepatocellular carcinoma HepG2 cells and its underlying mechanisms. Methods: The effects of Hydrangea serrata extract on growth inhibition of tumor cells and spheroids were assessed using MTT and 3D culture assays. Quantitative real-time PCR and Western blot analyses were employed to investigate the changes in mRNA and protein expression levels of molecules related to cell cycle and apoptosis. Results: Hydrangea serrata extract effectively inhibited the growth of both tumor cells and spheroids. The extract also significantly upregulated p27 mRNA expression and downregulated CDK2 mRNA expression, leading to cell cycle arrest. Moreover, increased BAX/Bcl-2 ratio as well as caspase-9 and -3 were observed after treatment with Hydrangea serrata extract, indicating the induction of tumor cell apoptosis. Conclusions: Hydrangea serrata extract has the potential to alleviate tumors by effectively modulating cell-cycle-related gene expressions and inducing apoptosis, thereby inhibiting tumor growth.

Keywords

Hydrangea serrata / Hepatocellular carcinoma / Liver cancer / Anticancer / Cell cycle arrest / Apoptosis

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Ye-eun Kim, Jeonghye Hwang, Ki-Young Kim. Hydrangea serrata extract exerts tumor inhibitory activity against hepatocellular carcinoma HepG2 cells via inducing p27/CDK2-mediated cell cycle arrest and apoptosis. Asian Pacific Journal of Tropical Biomedicine, 2024, 14 (2) : 65-72 DOI:10.4103/apjtb.apjtb_783_23

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Conflict of interest statement

The authors declare that they have no conflict of interest.

Funding

This research was funded by the GRRC Program of Gyeonggi province [GRRC-KyungHee2023(B01)], Republic of Korea.

Data availability statement

The data supporting the findings of this study are available from the corresponding authors upon request.

Authors’ contributions

Both YEK and JH wrote the manuscript, performed experiments, collected and analyzed data, and designed this study. KYK contributed to supervision and revision of the manuscript. All authors reviewed the final manuscript.

References

[1]

Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2021; 71(3): 209-249.

[2]

Llovet JM, Kelley RK, Villanueva A, Singal AG, Pikarsky E, Roayaie S, et al. Hepatocellular carcinoma. Nat Rev Dis Primers 2021; 7(1): 6.

[3]

El-Serag HB, Davila JA, Petersen NJ, McGlynn KA. The continuing increase in the incidence of hepatocellular carcinoma in the United States: An update. Ann Intern Med 2003; 139(10): 817-823.

[4]

Sia D, Villanueva A, Friedman SL, Llovet JM. Liver cancer cell of origin, molecular class, and effects on patient prognosis. Gastroenterology 2017; 152(4): 745-761.

[5]

Estes C, Razavi H, Loomba R, Younossi Z, Sanyal AJ. Modeling the epidemic of nonalcoholic fatty liver disease demonstrates an exponential increase in burden of disease. Hepatology 2018; 67(1): 123-133.

[6]

Jung CH, Kim Y, Kim MS, Lee S, Yoo SH. The establishment of efficient bioconversion, extraction, and isolation processes for the production of phyllodulcin, a potential high intensity sweetener, from sweet hydrangea leaves (Hydrangea macrophylla Thunbergii). Phytochem Anal 2016; 27(2): 140-147.

[7]

Han HS, Lee HH, Gil HS, Chung KS, Kim JK, Kim DH, et al. Standardized hot water extract from the leaves of Hydrangea serrata (Thunb.) Ser. alleviates obesity via the AMPK pathway and modulation of the gut microbiota composition in high fat diet-induced obese mice. Food Funct 2021; 12(6): 2672-2685.

[8]

Han HS, Shin JS, Myung DB, Ahn HS, Lee SH, Kim HJ, et al. Hydrangea serrata (Thunb.) Ser. extract attenuate UVB-induced photoaging through MAPK/AP-1 inactivation in human skin fibroblasts and hairless mice. Nutrients 2019; 11(3): 533.

[9]

Dilshara MG, Jayasooriya RG, Lee S, Jeong JB, Seo YT, Choi YH, et al. Water extract of processed Hydrangea macrophylla (Thunb.) Ser. leaf attenuates the expression of pro-inflammatory mediators by suppressing Akt-mediated NF-κB activation. Environ Toxicol Pharmacol 2013; 35(2): 311-319.

[10]

Akanda MR, Tae HJ, Kim IS, Ahn D, Tian W, Islam A, et al. Hepatoprotective role of Hydrangea macrophylla against sodium arsenite-induced mitochondrial-dependent oxidative stress via the inhibition of MAPK/Caspase-3 pathways. Int J Mol Sci 2017; 18(7). doi: 10.3390/ijms18071482.

[11]

Zhang H, Matsuda H, Yamashita C, Nakamura S, Yoshikawa M. Hydrangeic acid from the processed leaves of Hydrangea macrophylla var. thunbergii as a new type of anti-diabetic compound. Eur J Pharmacol 2009; 606(1-3): 255-261.

[12]

Hsieh CR, Yu PJ, Chen LG, Chaw SM, Chang CC, Wang CC. Cytotoxic constituents of Hydrangea angustipetala on human gastric carcinoma cells. Bot Sci 2010; 51: 45-51.

[13]

Yang YM, Kim SY, Seki E. Inflammation and liver cancer: Molecular mechanisms and therapeutic targets. Semin Liver Dis 2019; 39(1): 26-42.

[14]

Pirkmajer S, Chibalin AV. Serum starvation: Caveat emptor. Am J Physiol Cell Physiol 2011; 301(2): C272-C279.

[15]

Kim M, Kim JG, Kim KY. Trichosanthes kirilowii extract promotes wound healing through the phosphorylation of ERK1/2 in keratinocytes. Biomimetics 2022; 7(4). doi: 10.3390/biomimetics7040154.

[16]

Park SC, Kim JG, Shin YK, Kim KY. Antimicrobial activity of 4-hydroxyderricin, sophoraflavanone G, acetylshikonin, and kurarinone against the bee pathogenic bacteria Paenibacillus larvae and Melissococcus plutonius. J Apic Res 2021; 60(1): 118-122.

[17]

Badr-Eldin SM, Aldawsari HM, Kotta S, Deb PK, Venugopala KN. Three-dimensional in vitro cell culture models for efficient drug discovery: Progress so far and future prospects. Pharmaceuticals (Basel) 2022; 15(8). doi: 10.3390/ph15080926.

[18]

Kapałczyńska M, Kolenda T, Przybyła W, Zajączkowska M, Teresiak A, Filas V, et al. 2D and 3D cell cultures - a comparison of different types of cancer cell cultures. Arch Med Sci 2018; 14(4): 910-919.

[19]

Bresciani G, Hofland LJ, Dogan F, Giamas G, Gagliano T, Zatelli MC. Evaluation of spheroid 3D culture methods to study a pancreatic neuroendocrine neoplasm cell line. Front Endocrinol (Lausanne) 2019; 10. doi: 10.3389/fendo.2019.00682.

[20]

Kim YE, Kim KY, Min JW, Kim MJ, Kang HC. Exosomal AZGP1 as a new diagnostic marker candidate for pancreatic cancer. Biomark J 2022; 8(11): 162.

[21]

Hwang J, Moon H, Kim H, Kim KY. Identification of a novel ERK5 (MAPK7) inhibitor, MHJ-627, and verification of its potent anticancer efficacy in cervical cancer HeLa cells. Curr Issues Mol Biol 2023; 45(7): 6154-6169.

[22]

Nguyen AT, Kim M, Kim YE, Kim H, Lee S, Lee Y, et al. MSF enhances human antimicrobial peptide β-defensin (HBD2 and HBD3) expression and attenuates inflammation via the NF-κB and p38 signaling pathways. Molecules 2023; 28(6). doi: 10.3390/molecules28062744.

[23]

Wen Y, Mirji N, Irudayaraj J. Epigenetic toxicity of PFOA and GenX in HepG2 cells and their role in lipid metabolism. Toxicol In Vitro 2020; 65. doi: 10.1016/j.tiv.2020.104797.

[24]

Nguyen AT, Kim KY. Inhibition of proinflammatory cytokines in Cutibacterium acnes-induced inflammation in HaCaT cells by using Buddleja davidii aqueous extract. Int J Inflam 2020; 2020. doi: 10.1155/2020/8063289.

[25]

Kim M, Kim J, Shin YK, Kim KY. Gentisic acid stimulates keratinocyte proliferation through ERK1/2 phosphorylation. Int J Med Sci 2020; 17(5): 626-631.

[26]

Kim J, Shin YK, Kim KY. Promotion of keratinocyte proliferation by tracheloside through ERK1/2 stimulation. Evid Based Complement Alternat Med 2018; 2018. doi: 10.1155/2018/4580627.

[27]

Shin SS, Ko MC, Park YJ, Hwang B, Park SL, Kim WJ, et al. Hydrangenol inhibits the proliferation, migration, and invasion of EJ bladder cancer cells via p21WAF1-mediated G1-phase cell cycle arrest, p38 MAPK activation, and reduction in Sp-1-induced MMP-9 expression . EXCLI J 2018; 17: 531-543.

[28]

Hume S, Dianov GL, Ramadan K. A unified model for the G1/S cell cycle transition . Nucleic Acids Res 2020; 48(22): 12483-12501.

[29]

Guadagno TM, Newport JW. Cdk2 kinase is required for entry into mitosis as a positive regulator of Cdc2-cyclin B kinase activity. Cell 1996; 84(1): 73-82.

[30]

Davies C, Brown CM, Westphal D, Ward JM, Ward VK. Murine norovirus replication induces G0/G1 cell cycle arrest in asynchronously growing cells . J Virol 2015; 89(11): 6057-6066.

[31]

Park M, Krause MW. Regulation of postembryonic G(1) cell cycle progression in Caenorhabditis elegans by a cyclin D/CDK-like complex. Development 1999; 126(21): 4849-4860.

[32]

Misao J, Hayakawa Y, Ohno M, Kato S, Fujiwara T, Fujiwara H. Expression of bcl-2 protein, an inhibitor of apoptosis, and Bax, an accelerator of apoptosis, in ventricular myocytes of human hearts with myocardial infarction. Circulation 1996; 94(7): 1506-1512.

[33]

Raisova M, Hossini AM, Eberle J, Riebeling C, Wieder T, Sturm I, et al. The Bax/Bcl-2 ratio determines the susceptibility of human melanoma cells to CD95/Fas-mediated apoptosis. J Invest Dermatol 2001; 117(2): 333-340.

[34]

Wang Q, Zhang L, Yuan X, Ou Y, Zhu X, Cheng Z, et al. The relationship between the Bcl-2/Bax proteins and the mitochondria-mediated apoptosis pathway in the differentiation of adipose-derived stromal cells into neurons. PLoS One 2016; 11(10). doi: 10.1371/journal.pone.0163327.

[35]

Morales-Cano D, Calviño E, Rubio V, Herráez A, Sancho P, Tejedor MC, et al. Apoptosis induced by paclitaxel via Bcl-2, Bax and caspases 3 and 9 activation in NB4 human leukaemia cells is not modulated by ERK inhibition. Exp Toxicol Pathol 2013; 65(7-8): 1101-1108.

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