Research Article
BibTex RIS Cite

Phytochemical Screening, Antioxidant and Anticancer Activities of Euphorbia hyssopifolia L. against MDA-MB-231 Breast Cancer Cell Line

Year 2022, , 295 - 310, 28.02.2022
https://doi.org/10.18596/jotcsa.1021449

Abstract

Euphorbia hyssopifolia L. is an annual herb producing toxic latex. To our knowledge, this study is the first one that focuses on accurately identifying the bioactive compounds in E. hyssopifolia and evaluating its antioxidant and anti-breast cancer activities. Phytochemical qualitative screening tests were performed. Total phenolic contents (TPC) and total flavonoid contents (TFC) were determined by Folin Ciocalteu and Aluminum chloride methods, respectively. Bioactive compounds in E. hyssopifolia latex were identified by using GC-MS analysis. Antioxidant activity was evaluated using DPPH and ABTS assays, and anticancer activity of latex against MDA-MB-231 breast cancer cell line was studied using flow cytometry methods. Results revealed the presence of flavonoids, tannins, alkaloids, diterpenes, steroids, and cardiac glycosides in the plant, whereas saponins were absent. Latex outperformed methanolic 70% extract in terms of TPC and TFC (39.52 ± 0.36 mg GAE/g E and 28.66 ± 0.10 mg RE/g E, respectively). GC-MS analysis of E. hyssopifolia latex resulted in the identification of 26 compounds, of which triterpenoids constitute 67.0172%, followed by lupeol (23.7089%) and betulin (14.0098%). According to the reference studies, most of the compounds found in latex have many biological activities. Latex outperformed all extracts and ascorbic acid in terms of antioxidant activity (IC50= 0.029 mg/mL for DPPH, IC50= 0.001 mg/mL for ABTS). Flow cytometry methods revealed that E. hyssopifolia latex induced cell cycle arrest at G1 phase (61%) and apoptosis (21.93%) of MDA-MB-231 cells after treating with latex at 10 µg/mL for 24 hours. However, more studies should be performed to explore bioactive compounds in E. hyssopifolia and determine the underlying mechanism of its latex anti-breast cancer effects.

Supporting Institution

Atomic Energy Commission of Syria

Thanks

All the authors are thankful to Dr. Adnan Ikhtiar (main researcher in Biotechnology Department in Atomic Energy Commission of Syria) for his support and encouragement.

References

  • 1. Mabberley DJ. The plant book. Cambridge: Cambridge University Press; 1997.
  • 2. Prenner G, Rudall PJ. Comparative ontogeny of the cyathium in Euphorbia (Euphorbiaceae) and its allies: exploring the organ flower inflorescence boundary. American Journal of Botany. 2007;94(10):1612–29.
  • 3. Muthu C, Ayyanar M, Raja N, Ignacimuthu S. Medicinal plants used by traditional healers in Kancheepuram District of Tamil Nadu, India. Journal of Ethnobiology and Ethnomedicine. 2006;2(1):43.
  • 4. Kitajima S, Kamei K, Taketani S, Yamaguchi M, Kawai F, Komatsu A, et al. Two chitinase-like proteins abundantly accumulated in latex of mulberry show insecticidal activity. BMC Biochemistry. 2010;11(1):6.
  • 5. Mouterde P. Tome II. In: Nouvelle flore du Liban et de la Syrie. Beyrouth: Éd. de l’Impr. Catholique; 1966. p. 475–98.
  • 6. Bolaji AO, Olojede CB, Famurewa AA, Faluyi JO. Morphological and cytological studies of Euphorbia hyssopifolia L. and Euphorbia heterophylla L. from Ile-Ife, Nigeria. Nigerian Journal of Genetics. 2014;28(2):15–8.
  • 7. Ma J-S, Gilbert M. 4. Euphorbia hyssopifolia Linnaeus, Syst. Nat., ed. 10. 2: 1048. 1759. Flora of China; FOC. 2016;11:289–93.
  • 8. Babojian G. Recordation of Euphorbia hyssopifolia L. (Euphorbiaceae) a new alien Species for Flora of Syria. Damascus University Journal for Basic Sciences. 2018;34(1):121–47.
  • 9. Abo KA. Characterisation of ingenol: an inflammatory diterpene from some Nigerian Euphorbia and Elaeophorbia species. African Journal of Medicine and Medical Sciences. 1994;23(2):161–3.
  • 10. Adedapo AA, Abatan MO, i Olorunsogo OO. Toxic effects of some plants in the genus Euphorbia on haematological and biochemical parameters of rats. Veterinarski Arhiv. 2004;74(1):53–62.
  • 11. Igwenyi IO, Agwor AS, Nwigboji IU, Agbafor KN, Offor CE. Proximate Analysis, Mineral and Phytochemical Composition of Euphorbia Hyssopifolia. IOSR Journal of Dental and Medical Sciences. 2014;13(6):41–3.
  • 12. Araújo S de S, Fernandes TCC, Cardona YT, Almeida PM de, Marin-Morales MA, dos Santos AV, et al. Cytotoxic and genotoxic effects of ethanolic extract of Euphorbia hyssopifolia L. on HepG2 cells. Journal of Ethnopharmacology. 2015;170:16–9.
  • 13. Igwenyi I, Nwachukwu N, Mba O, Offor CE, Aja P, Ugwu O. Hepatoxicity effects of aqueous extract of Euphorbia hyssopifolia on selected tissues of albino rats. Fermentation Technology and Bioengineering. 2011;2:7–10.
  • 14. McGuire A, Brown J, Malone C, McLaughlin R, Kerin M. Effects of Age on the Detection and Management of Breast Cancer. Cancers. 2015;7(2):908–29.
  • 15. Bigoniya P, Shukla A, Singh CS. Dermal irritation and sensitization study of Euphorbia neriifolia latex and its anti-inflammatory efficacy. International Journal of Phytomedicine. 2010;2:3.
  • 16. Yener İ, Ertaş A, Yilmaz MA, Tokul Ölmez Ö, Köseoğlu Yılmaz P, Yeşil Y, et al. Characterization of the Chemical Profile of Euphorbia Species from Turkey by Gas Chromatography–Mass Spectrometry (GC-MS), Liquid Chromatography–Tandem Mass Spectrometry (LC-MS/MS), and Liquid Chromatography–Ion Trap–Time-of-Flight–Mass Spectrometry (LC-IT-TOF-MS) and Chemometric Analysis. Analytical Letters. 2019;52(7):1031–49.
  • 17. Shashikala M, Shah M, Pande M. Determination of Total Phenols and Flavonoid Content of Bryonia laciniosa by Spectrophotometric Method. Journal of Chemical and Pharmaceutical Research. 2018;10(12):30–4.
  • 18. Borah R, Biswas SP. Tulsi (Ocimum sanctum), excellent source of phytochemicals. International Journal of Environment, Agriculture and Biotechnology. 2018;3(5):1732–8.
  • 19. Gonfa T, Teketle S, Kiros T. Effect of extraction solvent on qualitative and quantitative analysis of major phyto-constituents and in-vitro antioxidant activity evaluation of Cadaba rotundifolia Forssk leaf extracts. Yildiz F, editor. Cogent Food & Agriculture. 2020;6(1):1853867.
  • 20. Archana P, Samatha T, Mahitha B, Chamundeswari NR. Preliminary phytochemical screening from leaf and seed extracts of Senna alata L. Roxb-an ethno medicinal plant. Int J Pharm Biol Res. 2012;3(3):82–9.
  • 21. Tadesse G, Reneela P, Dekebo A. Isolation and characterization of natural products from Helinus mystachnus (Rhamnaceae). J Chem Pharm Res. 2012;4(3):1756–62.
  • 22. Das SS. Studies on Qualitative Determination of Phytochemical Constituents and Antimicrobial Activities of Five Mangrove Plants. In: Mangroves of Indian Sundarban: Ecological, Biochemical and Molecular Aspects. Lulu Publication; 2021. p. 31. 23. Kumar Bargah R. Preliminary test of phytochemical screening of crude ethanolic and aqueous extract of Moringa pterygosperma Gaertn. Journal of Pharmacognosy and Phytochemistry. 2015;4(1):07–9.
  • 24. Sawant RS, Godghate AG. Qualitative phytochemical screening of rhizomes of Curcuma longa Linn. International Journal of Science, Environment and Technology. 2013;2(4):634–41.
  • 25. AlHafez M, Kheder F, AlJoubbeh M. Polyphenols, flavonoids and (-)-epigallocatechin gallate in tea leaves and in their infusions under various conditions. Nutrition & Food Science. 2014;44(5):455–63.
  • 26. Karimi A, Mohammadi-Kamalabadi M, Rafieian-Kopaei M, Amjad L, Salimzadeh L. Determination of antioxidant activity, phenolic contents and antiviral potential of methanol extract of Euphorbia spinidens Bornm (Euphorbiaceae). Tropical Journal of Pharmaceutical Research. 2016;15(4):759.
  • 27. Saka F Al, Karabet F, Daghestani M, Soukkarieh C. Composition, in vitro antioxidant and antileishmanial activities of Vitex agnus-castus L. and Thymus syriacus boiss. Essential Oils. International Journal of ChemTech Research. 2015;8(8):53–60.
  • 28. Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C. Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radical Biology and Medicine. 1999;26(9–10):1231–7.
  • 29. Evans FJ, Taylor SE. Pro-Inflammatory, Tumour-Promoting and Anti-Tumour Diterpenes of the Plant Families Euphorbiaceae and Thymelaeaceae. In: Fortschritte der Chemie organischer Naturstoffe/Progress in the Chemistry of Organic Natural Products. 1983. p. 1–99.
  • 30. Mahomoodally MF, Dall’Acqua S, Sinan KI, Sut S, Ferrarese I, Etienne OK, et al. Phenolic compounds analysis of three Euphorbia species by LC-DAD-MSn and their biological properties. Journal of Pharmaceutical and Biomedical Analysis. 2020;189:113477.
  • 31. Majid M, Khan MR, Shah NA, Haq IU, Farooq MA, Ullah S, et al. Studies on phytochemical, antioxidant, anti-inflammatory and analgesic activities of Euphorbia dracunculoides. BMC Complementary and Alternative Medicine. 2015;15(1):349.
  • 32. Dai J, Mumper RJ. Plant Phenolics: Extraction, Analysis and Their Antioxidant and Anticancer Properties. Molecules. 2010;15(10):7313–52.
  • 33. Galanakis CM, Goulas V, Tsakona S, Manganaris GA, Gekas V. A Knowledge Base for The Recovery of Natural Phenols with Different Solvents. International Journal of Food Properties. 2013;16(2):382–96.
  • 34. Abdel-Aty AM, Hamed MB, Salama WH, Ali MM, Fahmy AS, Mohamed SA. Ficus carica, Ficus sycomorus and Euphorbia tirucalli latex extracts: Phytochemical screening, antioxidant and cytotoxic properties. Biocatalysis and Agricultural Biotechnology. 2019;20:101199.
  • 35. Guo M-B, Wang D-C, Liu H-F, Chen L-W, Wei J-W, Lin Y, et al. Lupeol against high-glucose-induced apoptosis via enhancing the anti-oxidative stress in rabbit nucleus pulposus cells. European Spine Journal. 2018;27(10):2609–20.
  • 36. Gallo MBC, Sarachine MJ. Biological activities of lupeol. Int J Biomed Pharm Sci. 2009;3(1):46–66.
  • 37. Zhao J, Li R, Pawlak A, Henklewska M, Sysak A, Wen L, et al. Antitumor Activity of Betulinic Acid and Betulin in Canine Cancer Cell Lines. In Vivo. 2018;32(5):1081–8.
  • 38. Shamsabadipour S, Ghanadian M, Saeedi H, Rahimnejad MR, Mohammadi-Kamalabadi M, Ayatollahi SM, et al. Triterpenes and Steroids from Euphorbia denticulata Lam. With Anti-Herpes Symplex Virus Activity. Iranian Journal of Pharmaceutical Research : IJPR. 2013;12(4):759–67.
  • 39. Delinassios G. UVA-induced oxidative stress and DNA damage in human skin cells and photoprotection by antioxidant compounds. King’s College London (University of London); 2012.
  • 40. Kosobutskii VS. Pyrocatechol and its derivatives as antioxidants and prooxidants. Russian Journal of General Chemistry. 2014;84(5):839–42.
  • 41. Vazhappilly CG, Hodeify R, Siddiqui SS, Laham AJ, Menon V, El‐Awady R, et al. Natural compound catechol induces DNA damage, apoptosis, and G1 cell cycle arrest in breast cancer cells. Phytotherapy Research. 2021;35(4):2185–99.
  • 42. Velika B, Kron I. Antioxidant properties of benzoic acid derivatives against Superoxide radical. Free Radicals and Antioxidants. 2012;2(4):62–7.
  • 43. Sawale JA, Patel JR, Kori ML. Antioxidant Properties of Cycloartenol Isolated from Euphorbia neriifolia Leaves. Indian Journal of Natural Products. 2019;33(1):60–4.
  • 44. Zhang Z-L, Luo Z-L, Shi H-W, Zhang L-X, Ma X-J. Research advance of functional plant pharmaceutical cycloartenol about pharmacological and physiological activity. Zhongguo Zhong Yao Za Zhi= Zhongguo Zhongyao Zazhi= China Journal of Chinese Materia Medica. 2017;42(3):433–7.
  • 45. Hong G-L, Liu J-M, Zhao G-J, Wang L, Liang G, Wu B, et al. The reversal of paraquat-induced mitochondria-mediated apoptosis by cycloartenyl ferulate, the important role of Nrf2 pathway. Experimental Cell Research. 2013;319(18):2845–55.
  • 46. Romero-Estrada A, Maldonado-Magaña A, González-Christen J, Bahena SM, Garduño-Ramírez ML, Rodríguez-López V, et al. Anti-inflammatory and antioxidative effects of six pentacyclic triterpenes isolated from the Mexican copal resin of Bursera copallifera. BMC Complementary and Alternative Medicine. 2016;16(1):422.
  • 47. Simão da Silva KAB, Paszcuk AF, Passos GF, Silva ES, Bento AF, Meotti FC, et al. Activation of cannabinoid receptors by the pentacyclic triterpene α,β-amyrin inhibits inflammatory and neuropathic persistent pain in mice. Pain. 2011;152(8):1872–87.
  • 48. Duke JA. Dr. Duke’s Phytochemical and Ethnobotanical Databases. 1992.
  • 49. Júnior JSC, Ferraz ABF, Feitosa CM, Cito A, Freitas RM, Saffi J. Evaluation of antioxidant effects in vitro of garcinielliptone FC (GFC) isolated from Platonia insignis Mart. Journal of Medicinal Plants Research. 2011;5(2):293–9.
  • 50. Costa Júnior JS, de Almeida AAC, Ferraz A de BF, Rossatto RR, Silva TG, Silva PBN, et al. Cytotoxic and leishmanicidal properties of garcinielliptone FC, a prenylated benzophenone from Platonia insignis. Natural Product Research. 2013;27(4–5):470–4.
  • 51. Won S-J, Lin T-Y, Yen C-H, Tzeng Y-H, Liu H-S, Lin C-N, et al. A novel natural tautomeric pair of garcinielliptone FC suppressed nuclear factor κB and induced apoptosis in human colorectal cancer cells. Journal of Functional Foods. 2016;24:568–78.
  • 52. Huerth KA, Hawkes JE, Meyer LJ, Powell DL. The Scourge of the Spurge Family—An Imitator of Rhus Dermatitis. Dermatitis. 2016;27(6):372–81.
  • 53. Pitchai D, Roy A, Ignatius C. In vitro evaluation of anticancer potentials of lupeol isolated from Elephantopus scaber L. on MCF-7 cell line. Journal of Advanced Pharmaceutical Technology & Research. 2014;5(4):179.
  • 54. Asadi-Samani M, Rafieian-Kopaei M, Lorigooini Z, Shirzad H. The effect of Euphorbia szovitsii Fisch. & C.A.Mey extract on the viability and the proliferation of MDA-MB-231 cell line. Bioscience Reports. 2019;39(1):1–8.
Year 2022, , 295 - 310, 28.02.2022
https://doi.org/10.18596/jotcsa.1021449

Abstract

References

  • 1. Mabberley DJ. The plant book. Cambridge: Cambridge University Press; 1997.
  • 2. Prenner G, Rudall PJ. Comparative ontogeny of the cyathium in Euphorbia (Euphorbiaceae) and its allies: exploring the organ flower inflorescence boundary. American Journal of Botany. 2007;94(10):1612–29.
  • 3. Muthu C, Ayyanar M, Raja N, Ignacimuthu S. Medicinal plants used by traditional healers in Kancheepuram District of Tamil Nadu, India. Journal of Ethnobiology and Ethnomedicine. 2006;2(1):43.
  • 4. Kitajima S, Kamei K, Taketani S, Yamaguchi M, Kawai F, Komatsu A, et al. Two chitinase-like proteins abundantly accumulated in latex of mulberry show insecticidal activity. BMC Biochemistry. 2010;11(1):6.
  • 5. Mouterde P. Tome II. In: Nouvelle flore du Liban et de la Syrie. Beyrouth: Éd. de l’Impr. Catholique; 1966. p. 475–98.
  • 6. Bolaji AO, Olojede CB, Famurewa AA, Faluyi JO. Morphological and cytological studies of Euphorbia hyssopifolia L. and Euphorbia heterophylla L. from Ile-Ife, Nigeria. Nigerian Journal of Genetics. 2014;28(2):15–8.
  • 7. Ma J-S, Gilbert M. 4. Euphorbia hyssopifolia Linnaeus, Syst. Nat., ed. 10. 2: 1048. 1759. Flora of China; FOC. 2016;11:289–93.
  • 8. Babojian G. Recordation of Euphorbia hyssopifolia L. (Euphorbiaceae) a new alien Species for Flora of Syria. Damascus University Journal for Basic Sciences. 2018;34(1):121–47.
  • 9. Abo KA. Characterisation of ingenol: an inflammatory diterpene from some Nigerian Euphorbia and Elaeophorbia species. African Journal of Medicine and Medical Sciences. 1994;23(2):161–3.
  • 10. Adedapo AA, Abatan MO, i Olorunsogo OO. Toxic effects of some plants in the genus Euphorbia on haematological and biochemical parameters of rats. Veterinarski Arhiv. 2004;74(1):53–62.
  • 11. Igwenyi IO, Agwor AS, Nwigboji IU, Agbafor KN, Offor CE. Proximate Analysis, Mineral and Phytochemical Composition of Euphorbia Hyssopifolia. IOSR Journal of Dental and Medical Sciences. 2014;13(6):41–3.
  • 12. Araújo S de S, Fernandes TCC, Cardona YT, Almeida PM de, Marin-Morales MA, dos Santos AV, et al. Cytotoxic and genotoxic effects of ethanolic extract of Euphorbia hyssopifolia L. on HepG2 cells. Journal of Ethnopharmacology. 2015;170:16–9.
  • 13. Igwenyi I, Nwachukwu N, Mba O, Offor CE, Aja P, Ugwu O. Hepatoxicity effects of aqueous extract of Euphorbia hyssopifolia on selected tissues of albino rats. Fermentation Technology and Bioengineering. 2011;2:7–10.
  • 14. McGuire A, Brown J, Malone C, McLaughlin R, Kerin M. Effects of Age on the Detection and Management of Breast Cancer. Cancers. 2015;7(2):908–29.
  • 15. Bigoniya P, Shukla A, Singh CS. Dermal irritation and sensitization study of Euphorbia neriifolia latex and its anti-inflammatory efficacy. International Journal of Phytomedicine. 2010;2:3.
  • 16. Yener İ, Ertaş A, Yilmaz MA, Tokul Ölmez Ö, Köseoğlu Yılmaz P, Yeşil Y, et al. Characterization of the Chemical Profile of Euphorbia Species from Turkey by Gas Chromatography–Mass Spectrometry (GC-MS), Liquid Chromatography–Tandem Mass Spectrometry (LC-MS/MS), and Liquid Chromatography–Ion Trap–Time-of-Flight–Mass Spectrometry (LC-IT-TOF-MS) and Chemometric Analysis. Analytical Letters. 2019;52(7):1031–49.
  • 17. Shashikala M, Shah M, Pande M. Determination of Total Phenols and Flavonoid Content of Bryonia laciniosa by Spectrophotometric Method. Journal of Chemical and Pharmaceutical Research. 2018;10(12):30–4.
  • 18. Borah R, Biswas SP. Tulsi (Ocimum sanctum), excellent source of phytochemicals. International Journal of Environment, Agriculture and Biotechnology. 2018;3(5):1732–8.
  • 19. Gonfa T, Teketle S, Kiros T. Effect of extraction solvent on qualitative and quantitative analysis of major phyto-constituents and in-vitro antioxidant activity evaluation of Cadaba rotundifolia Forssk leaf extracts. Yildiz F, editor. Cogent Food & Agriculture. 2020;6(1):1853867.
  • 20. Archana P, Samatha T, Mahitha B, Chamundeswari NR. Preliminary phytochemical screening from leaf and seed extracts of Senna alata L. Roxb-an ethno medicinal plant. Int J Pharm Biol Res. 2012;3(3):82–9.
  • 21. Tadesse G, Reneela P, Dekebo A. Isolation and characterization of natural products from Helinus mystachnus (Rhamnaceae). J Chem Pharm Res. 2012;4(3):1756–62.
  • 22. Das SS. Studies on Qualitative Determination of Phytochemical Constituents and Antimicrobial Activities of Five Mangrove Plants. In: Mangroves of Indian Sundarban: Ecological, Biochemical and Molecular Aspects. Lulu Publication; 2021. p. 31. 23. Kumar Bargah R. Preliminary test of phytochemical screening of crude ethanolic and aqueous extract of Moringa pterygosperma Gaertn. Journal of Pharmacognosy and Phytochemistry. 2015;4(1):07–9.
  • 24. Sawant RS, Godghate AG. Qualitative phytochemical screening of rhizomes of Curcuma longa Linn. International Journal of Science, Environment and Technology. 2013;2(4):634–41.
  • 25. AlHafez M, Kheder F, AlJoubbeh M. Polyphenols, flavonoids and (-)-epigallocatechin gallate in tea leaves and in their infusions under various conditions. Nutrition & Food Science. 2014;44(5):455–63.
  • 26. Karimi A, Mohammadi-Kamalabadi M, Rafieian-Kopaei M, Amjad L, Salimzadeh L. Determination of antioxidant activity, phenolic contents and antiviral potential of methanol extract of Euphorbia spinidens Bornm (Euphorbiaceae). Tropical Journal of Pharmaceutical Research. 2016;15(4):759.
  • 27. Saka F Al, Karabet F, Daghestani M, Soukkarieh C. Composition, in vitro antioxidant and antileishmanial activities of Vitex agnus-castus L. and Thymus syriacus boiss. Essential Oils. International Journal of ChemTech Research. 2015;8(8):53–60.
  • 28. Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C. Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radical Biology and Medicine. 1999;26(9–10):1231–7.
  • 29. Evans FJ, Taylor SE. Pro-Inflammatory, Tumour-Promoting and Anti-Tumour Diterpenes of the Plant Families Euphorbiaceae and Thymelaeaceae. In: Fortschritte der Chemie organischer Naturstoffe/Progress in the Chemistry of Organic Natural Products. 1983. p. 1–99.
  • 30. Mahomoodally MF, Dall’Acqua S, Sinan KI, Sut S, Ferrarese I, Etienne OK, et al. Phenolic compounds analysis of three Euphorbia species by LC-DAD-MSn and their biological properties. Journal of Pharmaceutical and Biomedical Analysis. 2020;189:113477.
  • 31. Majid M, Khan MR, Shah NA, Haq IU, Farooq MA, Ullah S, et al. Studies on phytochemical, antioxidant, anti-inflammatory and analgesic activities of Euphorbia dracunculoides. BMC Complementary and Alternative Medicine. 2015;15(1):349.
  • 32. Dai J, Mumper RJ. Plant Phenolics: Extraction, Analysis and Their Antioxidant and Anticancer Properties. Molecules. 2010;15(10):7313–52.
  • 33. Galanakis CM, Goulas V, Tsakona S, Manganaris GA, Gekas V. A Knowledge Base for The Recovery of Natural Phenols with Different Solvents. International Journal of Food Properties. 2013;16(2):382–96.
  • 34. Abdel-Aty AM, Hamed MB, Salama WH, Ali MM, Fahmy AS, Mohamed SA. Ficus carica, Ficus sycomorus and Euphorbia tirucalli latex extracts: Phytochemical screening, antioxidant and cytotoxic properties. Biocatalysis and Agricultural Biotechnology. 2019;20:101199.
  • 35. Guo M-B, Wang D-C, Liu H-F, Chen L-W, Wei J-W, Lin Y, et al. Lupeol against high-glucose-induced apoptosis via enhancing the anti-oxidative stress in rabbit nucleus pulposus cells. European Spine Journal. 2018;27(10):2609–20.
  • 36. Gallo MBC, Sarachine MJ. Biological activities of lupeol. Int J Biomed Pharm Sci. 2009;3(1):46–66.
  • 37. Zhao J, Li R, Pawlak A, Henklewska M, Sysak A, Wen L, et al. Antitumor Activity of Betulinic Acid and Betulin in Canine Cancer Cell Lines. In Vivo. 2018;32(5):1081–8.
  • 38. Shamsabadipour S, Ghanadian M, Saeedi H, Rahimnejad MR, Mohammadi-Kamalabadi M, Ayatollahi SM, et al. Triterpenes and Steroids from Euphorbia denticulata Lam. With Anti-Herpes Symplex Virus Activity. Iranian Journal of Pharmaceutical Research : IJPR. 2013;12(4):759–67.
  • 39. Delinassios G. UVA-induced oxidative stress and DNA damage in human skin cells and photoprotection by antioxidant compounds. King’s College London (University of London); 2012.
  • 40. Kosobutskii VS. Pyrocatechol and its derivatives as antioxidants and prooxidants. Russian Journal of General Chemistry. 2014;84(5):839–42.
  • 41. Vazhappilly CG, Hodeify R, Siddiqui SS, Laham AJ, Menon V, El‐Awady R, et al. Natural compound catechol induces DNA damage, apoptosis, and G1 cell cycle arrest in breast cancer cells. Phytotherapy Research. 2021;35(4):2185–99.
  • 42. Velika B, Kron I. Antioxidant properties of benzoic acid derivatives against Superoxide radical. Free Radicals and Antioxidants. 2012;2(4):62–7.
  • 43. Sawale JA, Patel JR, Kori ML. Antioxidant Properties of Cycloartenol Isolated from Euphorbia neriifolia Leaves. Indian Journal of Natural Products. 2019;33(1):60–4.
  • 44. Zhang Z-L, Luo Z-L, Shi H-W, Zhang L-X, Ma X-J. Research advance of functional plant pharmaceutical cycloartenol about pharmacological and physiological activity. Zhongguo Zhong Yao Za Zhi= Zhongguo Zhongyao Zazhi= China Journal of Chinese Materia Medica. 2017;42(3):433–7.
  • 45. Hong G-L, Liu J-M, Zhao G-J, Wang L, Liang G, Wu B, et al. The reversal of paraquat-induced mitochondria-mediated apoptosis by cycloartenyl ferulate, the important role of Nrf2 pathway. Experimental Cell Research. 2013;319(18):2845–55.
  • 46. Romero-Estrada A, Maldonado-Magaña A, González-Christen J, Bahena SM, Garduño-Ramírez ML, Rodríguez-López V, et al. Anti-inflammatory and antioxidative effects of six pentacyclic triterpenes isolated from the Mexican copal resin of Bursera copallifera. BMC Complementary and Alternative Medicine. 2016;16(1):422.
  • 47. Simão da Silva KAB, Paszcuk AF, Passos GF, Silva ES, Bento AF, Meotti FC, et al. Activation of cannabinoid receptors by the pentacyclic triterpene α,β-amyrin inhibits inflammatory and neuropathic persistent pain in mice. Pain. 2011;152(8):1872–87.
  • 48. Duke JA. Dr. Duke’s Phytochemical and Ethnobotanical Databases. 1992.
  • 49. Júnior JSC, Ferraz ABF, Feitosa CM, Cito A, Freitas RM, Saffi J. Evaluation of antioxidant effects in vitro of garcinielliptone FC (GFC) isolated from Platonia insignis Mart. Journal of Medicinal Plants Research. 2011;5(2):293–9.
  • 50. Costa Júnior JS, de Almeida AAC, Ferraz A de BF, Rossatto RR, Silva TG, Silva PBN, et al. Cytotoxic and leishmanicidal properties of garcinielliptone FC, a prenylated benzophenone from Platonia insignis. Natural Product Research. 2013;27(4–5):470–4.
  • 51. Won S-J, Lin T-Y, Yen C-H, Tzeng Y-H, Liu H-S, Lin C-N, et al. A novel natural tautomeric pair of garcinielliptone FC suppressed nuclear factor κB and induced apoptosis in human colorectal cancer cells. Journal of Functional Foods. 2016;24:568–78.
  • 52. Huerth KA, Hawkes JE, Meyer LJ, Powell DL. The Scourge of the Spurge Family—An Imitator of Rhus Dermatitis. Dermatitis. 2016;27(6):372–81.
  • 53. Pitchai D, Roy A, Ignatius C. In vitro evaluation of anticancer potentials of lupeol isolated from Elephantopus scaber L. on MCF-7 cell line. Journal of Advanced Pharmaceutical Technology & Research. 2014;5(4):179.
  • 54. Asadi-Samani M, Rafieian-Kopaei M, Lorigooini Z, Shirzad H. The effect of Euphorbia szovitsii Fisch. & C.A.Mey extract on the viability and the proliferation of MDA-MB-231 cell line. Bioscience Reports. 2019;39(1):1–8.
There are 53 citations in total.

Details

Primary Language English
Subjects Chemical Engineering
Journal Section Articles
Authors

Asseel Azaat 0000-0001-7922-6106

Georget Babojian This is me 0000-0002-5744-9170

Nizar Issa This is me 0000-0003-0598-7513

Publication Date February 28, 2022
Submission Date November 10, 2021
Acceptance Date February 3, 2022
Published in Issue Year 2022

Cite

Vancouver Azaat A, Babojian G, Issa N. Phytochemical Screening, Antioxidant and Anticancer Activities of Euphorbia hyssopifolia L. against MDA-MB-231 Breast Cancer Cell Line. JOTCSA. 2022;9(1):295-310.