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Phytochemicals of Chrysophthalmum montanum (DC.) Boiss. Roots and Their Antiproliferative Activities Against HeLa and C6 Cell Lines

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Proceedings of the National Academy of Sciences, India Section B: Biological Sciences Aims and scope Submit manuscript

Abstract

Pre-fractionation and contemporary spectroscopic analysis provides important clues with regard to synergistic and antagonistic effects as well as biological activities in complex multi-mixtures, especially natural products. Phytochemical contents of the Chrysophthalmum montanum root extracts were analyzed by gas chromatography–mass spectrometry and high performance liquid chromatography–time of flight/mass spectrometry. Furthermore, biological activity of root extract was investigated by antiproliferative efficiencies against human uterus carcinoma and rat brain tumor cells in vitro. The biological activity tests were carried out as dose-dependent assay using a multiwell spectrophotometer. 5-Fluorouracil was used as standard anticancer drug. Total 61 lipophilic components were identified quantitatively from the sub-fraction of n-hexane in which saturated fatty acids (33.06%), unsaturated fatty acids (21.03%) and other organic components (43.35%). Twenty three hydrophilic components, 16 phenolic and 7 flavonoid compounds, were quantified in the hydrophilic sub-fractions obtained from the C. montanum roots. Among the hydrophilic components, the vanillic acid was analyzed as 46.463 ± 0.167 mg compound/g dry extract in the sub-fraction dichloromethane. The linoleic acid was analyzed as a substantial component (8.13%) in the sub-fraction n-hexane. The highest antiproliferative activities were obtained from the sub-fraction dichloromethane against HeLa cells (IC50 = 36.53 μg/mL) and the sub-fraction n-hexane against C6 cells (IC50 = 11.98 μg/mL). No cytotoxic effect was observed from these sub-fractions.

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References

  1. Selvi S, Paksoy MY, Polat R, Cakilcioglu U (2014) Micromorphological and anatomical characteristics of the Genus Chrysophthalmum Schultz Bip. (Asteraceae) growing in Turkey. Proc Natl Acad Sci India B 84:431–438

    Google Scholar 

  2. Kirbag S, Zengin F, Kursat M (2009) Antimicrobial activities of extracts of some plants. Pak J Bot 41:2067–2070

    Google Scholar 

  3. Arasan S, Kaya I (2015) Some important plants belonging to asteraceae family used in folkloric medicine in Savur (Mardin/Turkey) area and their application areas. J Food Nutr Res 3:337–340

    Google Scholar 

  4. Siriwardhana N, Kalupahana NS, Moustaid-Moussa N (2012) Health benefits of n-3 polyunsaturated fatty acids: eicosapentaenoic acid and docosahexaenoic acid. Adv Food Nutr Res 65:211–222

    Article  PubMed  Google Scholar 

  5. Bazinet RP, Laye S (2014) Polyunsaturated fatty acids and their metabolites in brain function and disease. Nat Rev Neurosci 15:771–785

    Article  CAS  PubMed  Google Scholar 

  6. Demirtas I, Gecibesler IH, Yaglioglu AS (2013) Antiproliferative activities of isolated flavone glycosides and fatty acids from Stachys byzantina. Phytochem Lett 6:209–214

    Article  CAS  Google Scholar 

  7. Yaglioglu AS, Demirtas I, Goren N (2014) Bioactivity-guided isolation of antiproliferative compounds from Centaurea carduiformis. Phytochem Lett 6:209–214

    Google Scholar 

  8. Adedapo AA, Adeoye BO, Sofidiya MO, Oyagbemi AA (2015) Antioxidant, antinociceptive and anti-inflammatory properties of the aqueous and ethanolic leaf extracts of Andrographis paniculata in some laboratory animals. J Basic Clin Physiol Pharmcol 26:327–334

    CAS  Google Scholar 

  9. Gupta R, Goyal R, Bhattacharya S, Dhar KL (2015) Antioxidative in vitro and antiosteoporotic activities of Prinsepia utilis Royle in female rats. Eur J Integr Med 7:157–163

    Article  Google Scholar 

  10. Öksüz S, Topcu G, Krawiec M, Watson WH (1997) Eudesmanolides and other constituents of Inula thapsoides. Phytochemistry 46:1131–1134

    Article  Google Scholar 

  11. Huo Y, Shi H, Wang M, Li X (2008) Complete assignments of 1H and 13C NMR spectral data for three sesquiterpenoids from Inula helenium. Magn Reson Chem 46:1208–1211

    Article  CAS  PubMed  Google Scholar 

  12. Cheng XR, Zhang SD, Wang CH, Ren J, Qin JJ, Tang X, Zhang WD (2013) Bioactive eudesmane and germacrane derivatives from Inula wissmanniana Hand.-Mazz. Phytochemistry 96:214–222

    Article  CAS  PubMed  Google Scholar 

  13. Topcu G, Öksüz S, Herz W, Diaz JG (1995) Structurally related guaianolides from Inula thapsoides. Phytochemistry 40:1717–1722

    Article  CAS  Google Scholar 

  14. Konishi T, Shimada Y, Nagao T, Okabe H, Konoshima T (2002) Antiproliferative sesquiterpene lactones from the roots of Inula helenium. Biol Pharm Bull 25:1370–1372

    Article  CAS  PubMed  Google Scholar 

  15. Lokhande PD, Gawaı KR, Kodam KM, Kuchekar BS, Chabukswar AR, Jagdale SC (2007) Antibacterial activity of isolated constituents and extract of roots of Inula racemosa. Res J Med Plant 1:7–12

    Article  CAS  Google Scholar 

  16. Gürbüz P, Dogan SD, Pasayeva L, Paksoy MY (2016) Guaiane-type sesquiterpene lactones from Chrysophthalmum montanum. Rec Natl Prod 10:714–720

    Google Scholar 

  17. Aytac Z, Anderberg AA (2001) A new species of Chrysophthalmum Schultz Bip. (Asteraceae-Inuleae) from Turkey. Bot J Linn Soc 137:211–214

    Article  Google Scholar 

  18. Tanriover N, Ulu MO, Sanus GZ, Bilir A, Canbeyli R, Oz B, Akar Z, Kuday C (2008) The effects of systemic and intratumoral interleukin-12 treatment in C6 rat glioma model. Neurol Res 30:511–517

    Article  CAS  PubMed  Google Scholar 

  19. Ozcan G, Ozsoylemez OD, Akman G, Khalilia W, Yetiz BT, Karagoz A, Melikoglu G, Anil S, Kultur S, Sutlupinar N (2016) Screening for antitumor activity of various plant extracts on HeLa and C 4-I cell lines. JBUON 21:1552

    PubMed  Google Scholar 

  20. Morales P, Maieves HA, Dias MI, Calhella RC, Sanchez-Mata MC, Santos-Buelga C, Ferreira IC (2017) Hovenia dulcis Thunb. pseudofruits as functional foods: phytochemicals and bioactive properties in different maturity stages. J Funct Food 29:37–45

    Article  CAS  Google Scholar 

  21. Ali BH, Blunden G (2003) Pharmacological and toxicological properties of Nigella sativa. Phytother Res 17:299–305

    Article  CAS  PubMed  Google Scholar 

  22. Ju J, Picinich SC, Yang Z, Zhao Y, Suh N, Kong AN, Yang CS (2009) Cancer preventive activities of tocopherols and tocotrienols. Carcinogenesis 205:1–62

    Google Scholar 

  23. Moreno MM, Olalla HM, Gimenez MR, Navarro AM, Rufian HJA (2015) Phenolic compounds and antioxidant activity of Spanish commercial grape juices. J Food Compos Anal 38:19–26

    Article  CAS  Google Scholar 

  24. Roleira FM, Tavares SEJ, Varela CL, Costa SC, Silva T, Garrido J, Borges F (2015) Plant derived and dietary phenolic antioxidants: anticancer properties. Food Chem 183:235–258

    Article  CAS  PubMed  Google Scholar 

  25. Erenler R, Sen O, Aksit H, Demirtas I, Yaglioglu AS, Elmastas M, Telci I (2016) Isolation and identification of chemical constituents from Origanum majorana and investigation of antiproliferative and antioxidant activities. J Sci Food Agric 96:822–836

    Article  CAS  PubMed  Google Scholar 

  26. Gomes CA, Girao CT, Andrade JL, Milhazes N, Borges F, Marques MPM (2003) Anticancer activity of phenolic acids of natural or synthetic origin: a structure-activity study. J Med Chem 46:5395–5401

    Article  CAS  PubMed  Google Scholar 

  27. Chahar MK, Sharma N, Dobhal MP, Joshi YC (2011) Flavonoids: a versatile source of anticancer drugs. Pharmacogn Rev 5:1–12

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Chan JSL, Asatiani MD, Sharvit LE, Trabelcy B, Barseghyan GS, Wasser SP (2015) Chemical composition and medicinal value of the new Ganoderma tsugae var. jannieae CBS-120304 medicinal higher basidiomycete mushroom. Int J Med Mushrooms 17:735–747

    Article  PubMed  Google Scholar 

  29. Kang HG, Jeong SH, Cho JH (2010) Antimutagenic and anticarcinogenic effect of methanol extracts of sweetpotato (Ipomea batata) leaves. Toxicol Res 26:29–35

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

The authors acknowledge the financial support of the Scientific Research Project, Department of Bingol University (Projects: BAP-21-217-2014 and BAP-21-322-2015). They also thank Dr. Alpaslan Kocak for the identification of plant material and Prof. Dr. Nazlı Arda and Associate Prof. Ali Karagöz for providing C6 and HeLa cell lines. They also thank Mr. Serkan Koldas for grammatical revision.

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Correspondence to I. H. Gecibesler.

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Significance statementChrysophthalmum montanum is used in the treatment of colds and sinuses. The apolar fractions rich in lipophilic components of C. montanum showed significant antiproliferative activities against HeLa and C6 cells as compared to 5-fluorouracil.

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Gecibesler, I.H., Yaglıoglu, A.S., Gul, F. et al. Phytochemicals of Chrysophthalmum montanum (DC.) Boiss. Roots and Their Antiproliferative Activities Against HeLa and C6 Cell Lines. Proc. Natl. Acad. Sci., India, Sect. B Biol. Sci. 89, 145–154 (2019). https://doi.org/10.1007/s40011-017-0925-1

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