Molecular Basis of Sida cordifolia (L.) Induced Apoptosis in Melanoma Cell Line

Jump To References Section

Authors

  • Department of Physiology, Tamil Nadu Dr MGR University of Health Sciences, Swamy Vivekananda Medical College Hospital and Research Institute, Tiruchengode - 637205, Tamil Nadu ,IN
  • Department of Physiology, Vinayaka Missions Research Foundation, Vinayaka Mission’s KV Medical College and Hospitals, Salem - 636308, Tamil Nadu ,IN
  • Department of Physiology, Tamil Nadu Dr MGR University of Health Sciences, Swamy Vivekananda Medical College Hospital and Research Institute, Tiruchengode - 637205, Tamil Nadu ,IN

DOI:

https://doi.org/10.18311/jnr/2024/33432

Keywords:

Bax, Bcl2, Caspase, Cell Cycle, Mitochondrial Membrane Potential

Abstract

Sida cordifolia of the family Malvaceae is widely used in traditional medicine for treating inflammation, respiratory and neurological ailments and wound healing. Its extract was found to possess effective antitumor activity in hepatocellular carcinoma and HeLa cell lines. This study was aimed at screening the anticancer activity of S. cordifolia and to investigate its mechanism of action. Aerial parts of the plant were subjected to hot continuous extraction by Soxhlet apparatus with ethanol as solvent. Cytotoxicity of the extract was assessed in various cancer cell lines viz. breast, ovarian, colon, skin, and liver cancer by MTT assay. For each cell line, the IC50 value was calculated. The mechanism of anticancer activity of the extract was studied in melanoma cells by exposing them to 12.5 and 25 μg/ml extract and comparing results with the control. Gel electrophoresis was used to analyse DNA laddering. Expression of TP53, Bcl and Caspase gene family proteins were determined by SDS-PAGE. Mitochondrial membrane potential was studied by the JC-1 kit. Cell cycle analysis was performed by using a flow cytometer. Statistical analysis was done by ANNOVA, and significant values were further analysed by Tucky post-hoc analysis. P value less than 0.05 was considered statistically significant. MTT assay revealed maximum cytotoxicity of the extract against melanoma with an IC50 value of 16.51μg/ml. Melanoma cells treated with the extract demonstrated dose-dependent DNA laddering. The extract also exhibited a dose-dependent increase in the level of Bax, Caspase 3, Caspase 9 and p53 proteins. Expression of Bcl2 protein was significantly reduced. Treatment of melanoma cells with the extract showed significant loss of mitochondrial membrane potential. Melanoma cell population in subG0 and G2/S was significantly elevated. From these results, we conclude that ethanol extract of S. cordifolia is cytotoxic to melanoma cells. It acts by inducing apoptosis via an intrinsic mechanism. The extract also arrests melanoma cells in the G2/M phase.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Published

2024-03-01

How to Cite

Bhutkar, P. M., Suganthi, V., & Bhutkar, M. V. (2024). Molecular Basis of <i>Sida cordifolia</i> (L.) Induced Apoptosis in Melanoma Cell Line. Journal of Natural Remedies, 24(3), 545–554. https://doi.org/10.18311/jnr/2024/33432

Issue

Section

Research Articles
Received 2023-03-30
Accepted 2024-01-03
Published 2024-03-01

 

References

WHO. Cancer. Available from: https://www.who.int/news-room/fact-sheets/detail/cancer [Accessed 13 Feb 2023]

Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA: A Cancer Journal for Clinicians. 2021; 71(3):209-49. https://doi.org/10.3322/caac.21660 PMid:33538338

Sultana S, Asif HM, Nazar HM, Akhtar N, Rehman JU, Rehman RU. Medicinal plants combating against cancer - A green anticancer approach. APJCP. 2014; 15(11):4385-94. https://doi.org/10.7314/APJCP.2014.15.11.4385 PMid:24969858

Iqbal J, Abbasi BA, Mahmood T, Kanwal S, Ali B, Shah SA, Khalil AT. Plant-derived anticancer agents: A green anticancer approach. Asian Pacific Journal of Tropical Biomedicine. 2017; 7(12):1129-50. https://doi.org/10.1016/j.apjtb.2017.10.016

Isoldi MC, Visconti MA, Castrucci AM. Anti-cancer drugs: Molecular mechanisms of action. Mini Reviews in Medicinal Chemistry. 2005; 5(7):685-95. https://doi.org/10.2174/1389557054368781 PMid:16026315

Akula R, Ravishankar GA. Influence of abiotic stress signals on secondary metabolites in plants. Plant Signalling and Behaviour. 2011; 6(11):1720-31. https://doi.org/10.4161/psb.6.11.17613 PMid:22041989 PMCid: PMC3329344

Karnofsky DA. Mechanism of action of anticancer drugs at a cellular level. CA: a cancer journal for clinicians. 1968; 18(4):232-4. https://doi.org/10.3322/canjclin.18.4.232 PMid:4992875

Prakash OM, Kumar A, Kumar P. Anticancer potential of plants and natural products. Am J Pharmacol Sci. 2013; 1(6):104-15. https://doi.org/10.12691/ajps-1-6-1

Srinithya B, Kumar VV, Vadivel V, Pemaiah B, Anthony SP, Muthuraman MS. Synthesis of biofunctionalized AgNPs using medicinally important S. cordifolia leaf extract for enhanced antioxidant and anticancer activities. Materials Letters. 2016; 170:101-4. https://doi.org/10.1016/j.matlet.2016.02.019

Auddy B, Ferreira M, Blasina F, Lafon L, Arredondo F, Dajas F, et al. Screening of antioxidant activity of three Indian medicinal plants, traditionally used for the management of neurodegenerative diseases. J Ethnopharmacol. 2003; 84(2-3):131-8. https://doi.org/10.1016/S0378-8741(02)00322-7 PMid:12648805

Momin MA, Bellah SF, Rahman SM, Rahman AA, Murshid GM, Emran TB. Phytopharmacological evaluation of ethanol extract of S. cordifolia L. roots. Asian Pacific Journal of Tropical Biomedicine. 2014; 4(1): 18-24. https://doi.org/10.1016/S2221-1691(14)60202-1 PMid:24144125

Pieme CA, Penlap VN, Ngogang J, Costache M. In vitro cytotoxicity and antioxidant activities of five medicinal plants of Malvaceae family from Cameroon. Environmental toxicology and pharmacology. 2010; 29(3):223-8. https://doi.org/10.1016/j.etap.2010.01.003 PMid:21787606

Yadav RN, Agarwala M. Phytochemical analysis of some medicinal plants. Journal of Phytology. 2011; 3(12):10-14.

Kumar P, Nagarajan A, Uchil PD. Analysis of cell viability by the MTT assay. Cold spring harbour protocols. 2018; 2018(6):pdb-rot095505. https://doi.org/10.1101/pdb.prot095505 PMid:29858338

Majtnerová P, Roušar T. An overview of apoptosis assays detecting DNA fragmentation. Molecular biology reports. 2018; 45:1469-78. https://doi.org/10.1007/s11033-018-4258-9 PMid:30022463

Sivandzade F, Bhalerao A, Cucullo L. Analysis of the mitochondrial membrane potential using the cationic JC-1 dye as a sensitive fluorescent probe. Bio-protocol. 2019; 9(1). https://doi.org/10.21769/BioProtoc.3128 PMid:30687773 PMCid: PMC6343665

Darzynkiewicz Z. Critical aspects in the analysis of cellular DNA content. Current protocols in cytometry. 2011; 56(1):7-2. https://doi.org/10.1002/0471142956.cy0702s56 PMid:21455968 PMCid: PMC3238682

Garnis C, Buys TP, Lam WL. Genetic alteration and gene expression modulation during cancer progression. Molecular Cancer. 2004; 3(1):1-23. https://doi.org/10.1186/1476-4598-3-1 PMid:14723797 PMCid: PMC324565

Abdel-Hameed ES, Bazaid SA, Shohayeb MM, El-Sayed MM, El-Wakil EA. Phytochemical studies and evaluation of antioxidant, anticancer and antimicrobial properties of Conocarpus erectus L. growing in Taif, Saudi Arabia. European Journal of Medicinal Plants. 2012; 2(2):93. https://doi.org/10.9734/EJMP/2012/1040

Saadat YR, Saeidi N, Vahed SZ, Barzegari A, Barar J. An update to DNA ladder assay for apoptosis detection. BioImpacts: BI. 2015; 5(1):25. https://doi.org/10.15171/bi.2015.01 PMid:25901294 PMCid: PMC4401164

Wong RS. Apoptosis in cancer: from pathogenesis to treatment. Journal of experimental and clinical cancer research. 2011; 30(1):1-4. https://doi.org/10.1186/1756-9966-30-87 PMid:21943236 PMCid: PMC3197541

Muthuraman MS, Sinsinwar S, Vetrivel U. Anticancer activity of S. cordifolia L., –insilico approach. Journal of Pharmaceutical Sciences and Research. 2017; 9(8):1363.

Mendoza Rodríguez CA, Cerbón MA. El gen supresor de tumores p53: mecanismos de acción en la proliferación y muerte celular. Rev Invest Clín. 2001; 53(3):266-73.

Palmieri G, Ombra M, Colombino M, Casula M, Sini M, Manca A, et al. Multiple molecular pathways in melanogenesis: characterization of therapeutic targets. Frontiers in Oncology. 2015; 5:183. https://doi.org/10.3389/fonc.2015.00183 PMid:26322273 PMCid: PMC4530319

Kiraz Y, Adan A, Yandim MK, Baran Y. Major apoptotic mechanisms and genes involved in apoptosis. Tumor Biology. 2016; 37(7):8471-86. https://doi.org/10.1007/s13277-016-5035-9 PMid:27059734

Zorova LD, Popkov VA, Plotnikov EY, Silachev DN, Pevzner IB, Jankauskas SS, et al. Mitochondrial membrane potential. Analytical biochemistry. 2018; 552:50-9. https://doi.org/10.1016/j.ab.2017.07.009 PMid:28711444 PMCid: PMC5792320

Ulukaya E, Pirianov G, Kurt MA, Wood EJ, Mehmet H. Fenretinide induces cytochrome c release, caspase 9 activation and apoptosis in the absence of mitochondrial membrane depolarization. Cell Death and Differentiation. 2003; 10(7):856-9. https://doi.org/10.1038/sj.cdd.4401242 PMid:12815470

Aithal MG, Rajeswari N. Bacoside A induced sub-G0 arrest and early apoptosis in human glioblastoma cell line U-87 MG through notch signalling pathway. Brain tumour research and treatment. 2019; 7(1):25-32. https://doi.org/10.14791/btrt.2019.7.e21 PMid:31062528 PMCid: PMC6504756

Shangguan WJ, Li H, Zhang YH. Induction of G2/M phase cell cycle arrest and apoptosis by ginsenoside Rf in human osteosarcoma MG63 cells through the mitochondrial pathway. Oncology reports. 2014; 31(1):305-13. https://doi.org/10.3892/or.2013.2815 PMid:24173574

Albuquerque KR, Pacheco NM, del Rosario LCT, de Melo FC, Novaes RD, Goncalves RV. Applicability of plant extracts in preclinical studies of melanoma: A systematic review. Mediators of inflammation. 2018; 2018:6797924. https://doi.org/10.1155/2018/6797924 PMid:30147443 PMCid: PMC6083739