In Vitro: Cytotoxicity, Apoptosis and Ameliorative Potential of Lawsonia inermis Extract in Human Lung, Colon and Liver Cancer Cell Line

References

• Nair L, Mahesh S, Smitha L, Sujathan K, Remani P. Expression of Canavalia gladiata lectin in leukemic cells. J Cancer Sci Ther. 2011;3:4.
   Google Scholar
• Bali A, Pal Singh M, Khorate M, Ahmed J. Malignant fibrous histiocytoma: an unusual transformation from benign to malignant. J Cancer Sci Ther. 2010;2(2):53–57. doi:10.4172/1948-5956.1000023.
   Google Scholar
• Ogale S, Yadav KS, Navale S. Screening of endophytic bacteria from the pharmacologically important medicinal plant Gloriosa superba for their multiple plant growth promoting properties. J Pharm Innov. 2018;7:208–214.
   Google Scholar
• Rosnah M, Asmah R, Maznah I, Asmah Y, Zanariah J, van Zurinah W. Effect of Lawsonia inermis (henna) on tumor marker enzyme activities during hepatocarcinogenesis in rats. J Biochem Mol Biol. 1998;3:25–29.
   Google Scholar
• Gupta S, Ali M, Alam MSJP. A naphthoquinone from Lawsonia inermis stem bark. Phytochemistry. 1993;33(3):723–724. doi:10.1016/0031-9422(93)85484-9.
   Web of Science ®Google Scholar
• Semwal RB, Semwal DK, Combrinck S, Cartwright-Jones C, Viljoen A. Lawsonia inermis L. (henna): ethnobotanical, phytochemical and pharmacological aspects. J Ethnopharmacol. 2014;155(1):80–103. doi:10.1016/j.jep.2014.05.042.
   PubMed Web of Science ®Google Scholar
• De Araújo MV, De Souza PS, De Queiroz AC, Da Matta CB, Leite AB, Da Silva AE, et al. Synthesis, leishmanicidal activity and theoretical evaluations of a series of substituted bis-2-hydroxy-1,4-naphthoquinones. Molecules. 2014;19(9):15180–15195. doi:10.3390/molecules190915180.
   PubMed Web of Science ®Google Scholar
• Pradhan R, Dandawate P, Vyas A, Padhye S, Biersack B, Schobert R, et al. From body art to anticancer activities: perspectives on medicinal properties of henna. Curr Drug Targets. 2012;13(14):1777–1798. doi:10.2174/138945012804545588.
   PubMed Web of Science ®Google Scholar
• Vargo-Gogola T, Rosen J. Modelling breast cancer: one size does not fit all. Nat Rev Cancer. 2007;7(9):659–672. doi:10.1038/nrc2193.
   PubMed Web of Science ®Google Scholar
• Ferreira D, Adega F, Chaves R. The importance of cancer cell lines as in vitro models in cancer methylome analysis and anticancer drugs testing. In: Oncogenomics and cancer proteomics: novel approaches in biomarkers discovery and therapeutic targets in cancer. London (UK): IntechOpen; 2013.
   Google Scholar
• Singh DK, Luqman S. Lawsonia inermis (L.): a perspective on anticancer potential of mehndi/henna. Biomed Res Ther. 2014;1(4):112–120. doi:10.7603/s40730-014-0018-1.
   Google Scholar
• Trigui M, Hsouna AB, Hammami I, Culioli G, Ksantini M, Tounsi S, et al. Efficacy of Lawsonia inermis leaves extract and its phenolic compounds against olive knot and crown gall diseases. Crop Prot. 2013;45:83–88. doi:10.1016/j.cropro.2012.11.014.
   Web of Science ®Google Scholar
• Rahmat A, Edrini S, Ismail P, Taufiq Y, Yun H, Abu Bakar M. Chemical constituents, antioxidant activity and cytotoxic effects of essential oil from Strobilanthes crispus and Lawsonia inermis. J Biol Sci. 2006;6(6):1005–1010. doi:10.3923/jbs.2006.1005.1010.
   Google Scholar
• Chirinos R, Rogez H, Campos D, Pedreschi R, Larondelle YJS, Technology P. Optimization of extraction conditions of antioxidant phenolic compounds from mashua (Tropaeolum tuberosum Ruíz & Pavón) tubers. Sep Purif Technol. 2007;55(2):217–225. doi:10.1016/j.seppur.2006.12.005.
   Web of Science ®Google Scholar
• Lafka T-I, Sinanoglou V, Lazos E. On the extraction and antioxidant activity of phenolic compounds from winery wastes. Food Chem. 2007;104(3):1206–1214. doi:10.1016/j.foodchem.2007.01.068.
   Web of Science ®Google Scholar
• Sadeghi-Aliabadi H, Ghasemi N, Kohi M. Cytotoxic effect of Convolvulus arvensis extracts on human cancerous cell line. Trop J Pharma Res. 2009;3(1):31–34.
   Google Scholar
• Oda Y, Nakashima S, Kondo E, Nakamura S, Yano M, Kubota C, et al. Comparison of lawsone contents among Lawsonia inermis plant parts and neurite outgrowth accelerators from branches. J Nat Med. 2018;72(4):890–896. doi:10.1007/s11418-018-1221-y.
   PubMed Web of Science ®Google Scholar
• Gundala SR, Yang C, Mukkavilli R, Paranjpe R, Brahmbhatt M, Pannu V, et al. Hydroxychavicol, a betel leaf component, inhibits prostate cancer through ROS-driven DNA damage and apoptosis. Toxicol Appl Pharmacol. 2014;280(1):86–96. doi:10.1016/j.taap.2014.07.012.
   PubMed Web of Science ®Google Scholar
• Schumacker P. Reactive oxygen species in cancer cells: live by the sword, die by the sword. Cancer Cell. 2006;10(3):175–176. doi:10.1016/j.ccr.2006.08.015.
   PubMed Web of Science ®Google Scholar
• Szatrowski TP, Nathan C. Production of large amounts of hydrogen peroxide by human tumor cells. Cancer Res. 1991;51(3):794–798.
   PubMed Web of Science ®Google Scholar
• Trachootham D, Alexandre J, Huang P. Targeting cancer cells by ROS-mediated mechanisms: a radical therapeutic approach? Nat Rev Drug Discov. 2009;8(7):579–591. doi:10.1038/nrd2803.
   PubMed Web of Science ®Google Scholar
• Spitz DR, Azzam EI, Li JJ, Gius DJC, Reviews M. Metabolic oxidation/reduction reactions and cellular responses to ionizing radiation: a unifying concept in stress response biology. Cancer Metastasis Rev. 2004;23(3–4):311–322. doi:10.1023/B:CANC.0000031769.14728.bc.
   PubMed Web of Science ®Google Scholar
• Conklin K. Cancer chemotherapy and antioxidants. J Nutr. 2004;134(11):3201S–3204S. doi:10.1093/jn/134.11.3201S.
   PubMed Web of Science ®Google Scholar
• Circu ML, Aw TY. Reactive oxygen species, cellular redox systems, and apoptosis. Free Radic Biol Med. 2010;48(6):749–762. doi:10.1016/j.freeradbiomed.2009.12.022.
   PubMed Web of Science ®Google Scholar
• Simon H-U, Haj-Yehia A, Levi-Schaffer FJA. Role of reactive oxygen species (ROS) in apoptosis induction. Apoptosis. 2000;5(5):415–418. doi:10.1023/A:1009616228304.
   PubMed Web of Science ®Google Scholar
• Thayyullathil F, Chathoth S, Hago A, Patel M, Galadari S. Rapid reactive oxygen species (ROS) generation induced by curcumin leads to caspase-dependent and -independent apoptosis in L929 cells. Free Radic Biol Med. 2008;45(10):1403–1412. doi:10.1016/j.freeradbiomed.2008.08.014.
   PubMed Web of Science ®Google Scholar
• Sharma V, Joseph C, Ghosh S, Agarwal A, Mishra MK, Sen E. Kaempferol induces apoptosis in glioblastoma cells through oxidative stress. Mol Cancer Ther. 2007;6(9):2544–2553. doi:10.1158/1535-7163.MCT-06-0788.
   PubMed Web of Science ®Google Scholar
• Métivier D, Dallaporta B, Zamzami N, Larochette N, Susin SA, Marzo I, et al. Cytofluorometric detection of mitochondrial alterations in early CD95/Fas/APO-1-triggered apoptosis of Jurkat T lymphoma cells. Comparison of seven mitochondrion-specific fluorochromes. Immunol Lett. 1998;61(2–3):157–163. doi:10.1016/S0165-2478(98)00013-3.
   PubMed Web of Science ®Google Scholar
• Zuliani T, Duval R, Jayat C, Schnébert S, André P, Dumas M, et al. Sensitive and reliable JC-1 and TOTO-3 double staining to assess mitochondrial transmembrane potential and plasma membrane integrity: interest for cell death investigations. Cytometry A. 2003;54(2):100–108. doi:10.1002/cyto.a.10059.
   PubMedGoogle Scholar
• Kamei H, Koide T, Kojima T, Hashimoto Y, Hasegawa M. Inhibition of cell growth in culture by quinones. Cancer Biother Radiopharm. 1998;13(3):185–188. doi:10.1089/cbr.1998.13.185.
   PubMed Web of Science ®Google Scholar
• Chien C-M, Lin K-L, Su J-C, Chuang P-W, Tseng C-H, Chen Y-L, et al. Naphtho[1,2-b]furan-4,5-dione induces apoptosis of oral squamous cell carcinoma: involvement of EGF receptor/PI3K/Akt signaling pathway. Eur J Pharmacol. 2010;636(1–3):52–58. doi:10.1016/j.ejphar.2010.03.030.
   PubMed Web of Science ®Google Scholar
• Xavier MR, Santos MMS, Queiroz MG, de Lima Silva MS, Goes AJS, De Morais Jr MA. Lawsone, a 2-hydroxy-1,4-naphthoquinone from Lawsonia inermis (henna), produces mitochondrial dysfunctions and triggers mitophagy in Saccharomyces cerevisiae. Mol Biol Rep. 2020;47(2):1173–1185. doi:10.1007/s11033-019-05218-3.
   PubMed Web of Science ®Google Scholar