References
- Antonio, P.D., et al., 2012. Scale-independent roughness value of cell membranes studied by means of AFM technique. Biochimica et Biophysica Acta (BBA) - Biomembranes, 1818 (12), 3141–3148.
- Buys, A., et al., 2013. Changes in red blood cell membrane structure in type 2 diabetes: a scanning electron and atomic force microscopy study. Cardiovascular Diabetology, 12 (1), 25.
- Calabrese, E.J., and Baldwin, L.A., 2002. Defining hormesis. Human & Experimental Toxicology, 21 (2), 91–97.
- Chang, C.-H., Lee, H.-H., and Lee, C.-H., 2017. Substrate properties modulate cell membrane roughness by way of actin filaments. Scientific Reports, 7 (1), 9068.
- Chen, M., et al., 2020. Examination of the relationship between viscoelastic properties and the invasion of ovarian cancer cells by atomic force microscopy. Beilstein Journal of Nanotechnology, 11, 568–582.
- Choudhari, A.S., et al., 2020. Phytochemicals in cancer treatment: from preclinical studies to clinical practice. Frontiers in Pharmacology, 10, 1614.
- Dufrêne, Y.F., et al., 2017. Imaging modes of atomic force microscopy for application in molecular and cell biology. Nature Nanotechnology, 12 (4), 295–307.
- Escribá, P.V., et al., 2015. Membrane lipid therapy: modulation of the cell membrane composition and structure as a molecular base for drug discovery and new disease treatment. Progress in Lipid Research, 59, 38–53.
- Faheina-Martins, G.V., et al., 2011. Influence of fetal bovine serum on cytotoxic and genotoxic effects of lectins in MCF-7 cells. Journal of Biochemical and Molecular Toxicology, 25 (5), 290–296.
- Franken, N.A.P., et al., 2006. Clonogenic assay of cells in vitro. Nature Protocols, 1 (5), 2315–2319.
- Fujii, Y., et al., 2019. Elucidation of the interaction between flavan-3-ols and bovine serum albumin and its effect on their in-vitro cytotoxicity. Molecules, 24 (20), 3667.
- Geng, R., et al., 2018. Influence of bovine serum albumin-flavonoid interaction on the antioxidant activity of dietary flavonoids: new evidence from electrochemical quantification. Molecules, 24 (1), 70.
- Greenwell, M., and Rahman, P.K.S.M., 2015. Medicinal plants: their use in anticancer treatment. International Journal of Pharmaceutical Sciences and Research, 6 (10), 4103–4112.
- Gurova, K., 2009. New hopes from old drugs: revisiting DNA-binding small molecules as anticancer agents. Future Oncology (London, England), 5 (10), 1685–1704.
- Hu, Y.J., et al., 2012. Molecular spectroscopic studies on the interaction of morin with bovine serum albumin. Journal of Photochemistry and Photobiology. B, Biology, 112, 16–22.
- Kabała-Dzik, A., et al., 2017. Migration rate inhibition of breast cancer cells treated by caffeic acid and caffeic acid phenethyl ester: an in vitro comparison study. Nutrients, 9 (10), 1144.
- Knöpfl-Sidler, F., et al., 2005. Human cancer cells exhibit in vitro individual receptiveness towards different mistletoe extracts. Die Pharmazie, 60 (6), 448–454.
- Lekka, M., and Laidler, P., 2009. Applicability of AFM in cancer detection. Nature Nanotechnology, 4 (2), 72–72.
- de Lima, C.A., et al., 2022. Antiproliferative activity of two unusual dimeric flavonoids, brachydin E and brachydin F, isolated from Fridericia platyphylla (Cham.) L.G. Lohmann: in vitro and molecular docking evaluation. BioMed Research International, 2022, 1–12.
- Lin, Y., et al., 2017. The interaction of serum albumin with ginsenoside Rh2 resulted in the downregulation of ginsenoside Rh2 cytotoxicity. Journal of Ginseng Research, 41 (3), 330–338.
- Liu, E.-H., Qi, L.-W., and Li, P., 2010. Structural relationship and binding mechanisms of five flavonoids with bovine serum albumin. Molecules (Basel, Switzerland), 15 (12), 9092–9103.
- Martin, F., et al., 2008. Antioxidant C-glucosylxanthones from the leaves of Arrabidaea patellifera. Journal of Natural Products, 71 (11), 1887–1890.
- Morris, G.M., et al., 2009. AutoDock4 and AutoDockTools4: automated docking with selective receptor flexibility. Journal of Computational Chemistry, 30 (16), 2785–2791.
- Nunes, H.L., et al., 2020. Characterization of the invitro cytotoxic effects of brachydins isolated from Fridericia platyphylla in a prostate cancer cell line. Journal of Toxicology and Environmental Health. Part A, 83 (15-16), 547–558.
- de Oliveira, L.C.B., et al., 2021. Aglycone flavonoid brachydin A shows selective cytotoxicity and antitumoral activity in human metastatic prostate (DU145) cancer cells. Cytotechnology, 73 (6), 761–774.
- Pal, S., and Saha, C., 2014. A review on structure-affinity relationship of dietary flavonoids with serum albumins. Journal of Biomolecular Structure & Dynamics, 32 (7), 1132–1147.
- Pillet, F., et al., 2014. Atomic force microscopy and pharmacology: from microbiology to cancerology. Biochimica et Biophysica Acta, 1840 (3), 1028–1050.
- Raudenska, M., et al., 2019. Cisplatin enhances cell stiffness and decreases invasiveness rate in prostate cancer cells by actin accumulation. Scientific Reports, 9 (1), 1660.
- Ravi, L., and Krishnan, K., 2016. A handbook on protein-ligand docking tool: AutoDock 4. Journal of the Medical Sciences, 4, 28–33.
- Rayan, A., Raiyn, J., and Falah, M., 2017. Nature is the best source of anticancer drugs: indexing natural products for their anticancer bioactivity. PLOS One, 12 (11), e0187925.
- Resende, F.A., et al., 2017. In vitro toxicological assessment of Arrabidaea brachypoda (DC.) bureau: mutagenicity and estrogenicity studies. Regulatory Toxicology and Pharmacology: RTP, 90, 29–35.
- Reuvers, T.G.A., Kanaar, R., and Nonnekens, J., 2020. DNA damage-inducing anticancer therapies: from global to precision damage. Cancers, 12 (8), 2098.
- Ribéreau-Gayon, G., et al., 1995. Effect of fetal calf serum on the cytotoxic activity of mistletoe (Viscum album L.) lectins in cell culture. Phytotherapy Research, 9 (5), 336–339.
- da Rocha, C.Q., et al., 2014. Dimeric flavonoids from Arrabidaea brachypoda and assessment of their anti-trypanosoma cruzi activity. Journal of Natural Products, 77 (6), 1345–1350.
- da Rocha, C.Q., et al., 2011. Anti-inflammatory and antinociceptive effects of Arrabidaea brachypoda (DC.) bureau roots. Journal of Ethnopharmacology, 133 (2), 396–401.
- Rocha, V., et al., 2018. Antileishmanial activity of dimeric flavonoids isolated from Arrabidaea brachypoda. Molecules, 24 (1), 1.
- Salgado, C., et al., 2020. In Vitro anti-inflammatory activity in arthritic Synoviocytes of A. brachypoda root extracts and its unusual dimeric flavonoids. Molecules, 25 (21), 5219.
- Serpeloni, J., et al., 2020. Fridericia platyphylla (Cham.) L.G. Lohmann root extract exerts cytotoxic and antiproliferative effects on gastric tumor cells and downregulates BCL-XL, BIRC5, and MET genes. Human & Experimental Toxicology, 39 (3), 338–354.
- Siddiqui, A.J., et al., 2022. Plants in anticancer drug discovery: from molecular mechanism to chemoprevention. BioMed Research International, 2022, 5425485–5425418.
- Singh, N.P., et al., 1988. A simple technique for quantitation of low levels of DNA damage in individual cells. Experimental Cell Research, 175 (1), 184–191.
- de Sousa Andrade, L.M., et al., 2020. Antimicrobial activity and inhibition of the NorA efflux pump of Staphylococcus aureus by extract and isolated compounds from Arrabidaea brachypoda. Microbial Pathogenesis, 140, 103935.
- Steeg, P.S., and Theodorescu, D., 2008. Metastasis: a therapeutic target for cancer. Nature Clinical Practice. Oncology, 5 (4), 206–219.
- Sung, H., et al., 2021. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA: A Cancer Journal for Clinicians, 71 (3), 209–249.
- Tan, L.T.H., et al., 2017. Targeting membrane lipid a potential cancer cure? Frontiers in Pharmacology, 8, 12.
- Tang, F., et al., 2017. Fetal bovine serum influences the stability and bioactivity of resveratrol analogues: a polyphenol-protein interaction approach. Food Chemistry, 219, 321–328.
- Tice, R.R., et al., 2000. Single cell gel/comet assay: guidelines for in vitro and in vivo genetic toxicology testing. Environmental and Molecular Mutagenesis, 35 (3), 206–221.
- Tsuchiya, H., 2010. Structure-dependent membrane interaction of flavonoids associated with their bioactivity. Food Chemistry, 120 (4), 1089–1096.
- Tsuchiya, H., 2015. Membrane interactions of phytochemicals as their molecular mechanism applicable to the discovery of drug leads from plants. Molecules (Basel, Switzerland), 20 (10), 18923–18966.
- Vichai, V., and Kirtikara, K., 2006. Sulforhodamine B colorimetric assay for cytotoxicity screening. Nature Protocols, 1 (3), 1112–1116.
- Wang, J., et al., 2009. Atomic force microscope study of tumor cell membranes following treatment with anti-cancer drugs. Biosensors & Bioelectronics, 25 (4), 721–727.
- Wang, J., et al., 2020. Graphene oxide inhibits cell migration and invasion by destroying actin cytoskeleton in cervical cancer cells. Aging, 12 (17), 17625–17633.
- Wang, X., Zhang, H., and Chen, X., 2019. Drug resistance and combating drug resistance in cancer. Cancer Drug Resistance, 2 (2), 141–160.
- Wang, Y., et al., 2016. Quantitative analysis of the cell-surface roughness and viscoelasticity for breast cancer cells discrimination using atomic force microscopy. Scanning, 38 (6), 558–563.
- Wu, J., et al., 2021. Plasticity of cancer cell invasion: patterns and mechanisms. Translational Oncology, 14 (1), 100899.
- Yang, F., et al., 2013. Anti-tumor activity evaluation of novel chrysin-organogermanium (IV) complex in MCF-7 cells. Bioorganic & Medicinal Chemistry Letters, 23 (20), 5544–5551.
- Yeow, N., Tabor, R.F., and Garnier, G., 2017. Atomic force microscopy: from red blood cells to immunohaematology. Advances in Colloid and Interface Science, 249, 149–162.
- Yue, P.Y.K., et al., 2010. A simplified method for quantifying cell migration/wound healing in 96-well plates. Journal of Biomolecular Screening, 15 (4), 427–433.