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image of Cytotoxic Effects of Dysphania ambrosioides Extracts on Oral Squamous Cell Carcinoma

Abstract

Introduction

, commonly known as “mastruz,” is a medicinal plant traditionally used for its therapeutic properties, including antimicrobial and anti-inflammatory effects. Previous studies have also suggested its antitumor potential. However, its role in oral squamous cell carcinoma (OSCC) remains unexplored. This study aimed to evaluate the cytotoxic effects of extracts on SCC4 (OSCC) and HaCaT (human keratinocyte) cell lines.

Methods

Crude extracts were obtained using different methods, including hexanic, ethanolic, hydroethanolic (7:3), and aqueous extractions, all performed ultrasonic-assisted extraction. The extracts were tested at concentrations ranging from 7.81 µg/mL to 1000 µg/mL using 2-fold serial dilutions. Cell viability was assessed after 48 hours of treatment using the MTT assay, with DMSO as the control.

Results

The extracts exhibited concentration-dependent cytotoxic effects on both cell lines, with HaCaT cells showing greater sensitivity. However, the lack of selectivity toward tumor cells over normal cells suggests a broad-spectrum cytotoxic activity without tumor-specific therapeutic targeting.

Conclusion

These findings highlight the need for further fractionation of the extracts and identification of the bioactive compounds responsible for the observed effects. Although the extracts demonstrated significant cytotoxic activity, their therapeutic potential should not be limited to cytotoxicity alone. Future studies should explore additional biological activities, such as anti-inflammatory or immunomodulatory properties, to fully understand the therapeutic applications of .

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2025-05-02
2025-11-05
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References

  1. Barros L. Pereira E. Calhelha R.C. Dueñas M. Carvalho A.M. Santos-Buelga C. Ferreira I.C.F.R. Bioactivity and chemical characterization in hydrophilic and lipophilic compounds of Chenopodium ambrosioides L. J. Funct. Foods 2013 5 4 1732 1740 10.1016/j.jff.2013.07.019
    [Google Scholar]
  2. Rios CEP Abreu A.G. Filho JAFB Nascimento J.R. Guerra RNM Amaral FMM Maciel MCG Nascimento F.R.F. Improves phagocytic activity and decreases bacterial growth and the systemic inflammatory response in sepsis induced by cecal ligation and puncture Chenopodium ambrosioides L. Front. Microbiol. 2017 8 148 10.3389/fmicb.2017.00148 28203235
    [Google Scholar]
  3. Kasali F.M. Tusiimire J. Kadima J.N. Agaba A.G. Ethnomedical uses, chemical constituents, and evidence-based pharmacological properties of Chenopodium ambrosioides L.: Extensive overview. Fut. J. Pharmaceut. Sci. 2021 7 1 153 10.1186/s43094‑021‑00306‑3
    [Google Scholar]
  4. Huang J. Hao J. Nie J. Qian R. Li H. Zhao J. Wang Y. Possible mechanism of Dysphania ambrosioides (L.) Mosyakin & Clemants seed extract suppresses the migration and invasion of human hepatocellular carcinoma cells SMMC-7721. Chem. Biodivers. 2023 20 3 e202200768 10.1002/cbdv.202200768 36694378
    [Google Scholar]
  5. Zohra T. Ovais M. Khalil A.T. Qasim M. Ayaz M. Shinwari Z.K. Extraction optimization, total phenolic, flavonoid contents, HPLC-DAD analysis and diverse pharmacological evaluations of Dysphania ambrosioides (L.) Mosyakin & Clemants. Nat. Prod. Res. 2019 33 1 136 142 10.1080/14786419.2018.1437428 29430965
    [Google Scholar]
  6. Rui-Hua Q. Xiao-Huan Z. Jun-Mei H. Jun-Mei H. Hai-Ying L. Bo-Han S. Qiu-Rong R. Zhao-Bin C. Zhao-Bin C. Dan-Wei M. Ya-Nan W. Essential oil from Chenopodium ambrosioides L. induces mitochondrial-mediated pathway and endoplasmic reticulum stress-related apoptosis in human liver cancer SMMC-7721 cells. Trop. J. Pharm. Res. 2020 19 4 837 843 10.4314/tjpr.v19i4.23
    [Google Scholar]
  7. Li J. Si C. Hong W. Xia C. Yang Y. He Y. Su M. Long X. Zhang H. Identification of the chemical components of ethanol extract of Chenopodium ambrosioides and evaluation of their in vitro antioxidant and anti tumor activities. Trop. J. Pharm. Res. 2022 21 8 1689 1697 10.4314/tjpr.v21i8.16
    [Google Scholar]
  8. Degenhardt R.T. Farias I.V. Grassi L.T. Franchi G.C. Nowill A.E. Da S. Bittencourt C.M. Wagner T.M. De Souza M.M. Cruz A.B. Malheiros A. Characterization and evaluation of the cytotoxic potential of the essential oil of Chenopodium ambrosioides. Rev. Bras. Farmacogn. 2016 26 1 56 61 10.1016/j.bjp.2015.08.012
    [Google Scholar]
  9. Pandiangan D. Lamlean P.Y. Maningkas P.F. Nainggolan N. Unitly A.J.A. Antioxidant and anticancer activity tests of “pasote” leaf water extracts (Dysphania ambrosioides L.) by in vitro method in leukemia cancer cells. J. Phys. Conf. Ser. 2020 1463 1 012020 10.1088/1742‑6596/1463/1/012020
    [Google Scholar]
  10. Jia-liang W. Dan-wei M. Ya-nan W. Hong Z. Bing H. Qun L. Zhi-yan Z. Jing F. Cytotoxicity of essential oil of Chenopodium ambrosioides L against human breast cancer MCF-7 cells. Trop. J. Pharm. Res. 2014 12 6 929 10.4314/tjpr.v12i6.10
    [Google Scholar]
  11. Ya-Nan W. Jia-Liang W. Dan-Wei M. Jiao L. Du-Yu Z. Anticancer effects of Chenopodium ambrosiodes L. essential oil on human breast cancer mcf-7 cells in vitro. Trop. J. Pharm. Res. 2015 14 10 1813 10.4314/tjpr.v14i10.11
    [Google Scholar]
  12. Tauchen J. Huml L. Bortl L. Doskocil I. Jarosova V. Marsik P. Frankova A. Clavo Peralta Z.M. Chuspe Zans M.E. Havlik J. Lapcik O. Kokoska L. Screening of medicinal plants traditionally used in Peruvian Amazon for in vitro antioxidant and anticancer potential. Nat. Prod. Res. 2019 33 18 2718 2721 10.1080/14786419.2018.1462180 29658320
    [Google Scholar]
  13. Silva I.A. Mendes D.P.D.C. Abreu C.R.C. Therapeutic and pharmacological aspects in the use of Chenopodium ambrosioides L. JRG J. Acad. Stud. 2020 3 7 4271881 10.5281/ZENODO.4271881
    [Google Scholar]
  14. Cruz GVB Pereira PVS Patrício FJ Costa G.C. Sousa SM Frazão J.B. Aragão-Filho W.C. Maciel M.C.G. Silva L.A. Amaral F.M.M. Barroqueiro E.S.B. Guerra R.N.M. Nascimento F.R.F. Increase of cellular recruitment, phagocytosis ability and nitric oxide production induced by hydroalcoholic extract from Chenopodium ambrosioides leaves. J. Ethnopharmacol. 2007 111 1 148 154 10.1016/j.jep.2006.11.006 17156956
    [Google Scholar]
  15. da Silva M.G.C. Amorim R.N.L. Câmara C.C. Fontenele Neto J.D. Soto-Blanco B. Acute and sub-chronic toxicity of aqueous extracts of Chenopodium ambrosioides leaves in rats. J. Med. Food 2014 17 9 979 984 10.1089/jmf.2013.0134 24892475
    [Google Scholar]
  16. Mosmann T. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J. Immunol. Meth. 1983 64 1-2 55 63 10.1016/0022‑1759(83)90303‑4
    [Google Scholar]
  17. Gaobotse G. Venkataraman S. Brown P.D. The use of African medicinal plants in cancer management. Front. Pharmacol. 2023 14 1122388 10.3389/fphar.2023.1122388
    [Google Scholar]
  18. Njoya EM Eloff J.N. McGaw L.J. Croton gratissimus leaf extracts inhibit cancer cell growth by inducing caspase 3/7 activation with additional anti-inflammatory and antioxidant activities. BMC Complement. Altern. Med. 2018 18 1 305 10.1186/s12906‑018‑2372‑9 30428879
    [Google Scholar]
  19. Suffness M, Pezzuto JM. Assays related to cancer drug discovery. In: Methods in plant biochemistry: assays for bioactivity. Hostettmann K, Ed. London: Academic Press 1990; pp. 71-133
  20. Lee H.M. Patel V. Shyur L.F. Lee W.L. Copper supplementation amplifies the anti-tumor effect of curcumin in oral cancer cells. Phytomedicine 2016 23 12 1535 1544 10.1016/j.phymed.2016.09.005 27765374
    [Google Scholar]
  21. Nascimento F.R.F. Cruz G.V.B. Pereira P.V.S. Maciel M.C.G. Silva L.A. Azevedo A.P.S. Barroqueiro E.S.B. Guerra R.N.M. Ascitic and solid Ehrlich tumor inhibition by Chenopodium ambrosioides L. treatment. Life Sci. 2006 78 22 2650 2653 10.1016/j.lfs.2005.10.006 16307762
    [Google Scholar]
  22. Jesus R.S. Piana M. Freitas R.B. Brum T.F. Alves C.F.S. Belke B.V. Mossmann N.J. Cruz R.C. Santos R.C.V. Dalmolin T.V. Bianchini B.V. Campos M.M.A. Bauermann L.F. In vivo antimicrobial and antimycobacterial activity and HPLC–DAD screening of phenolics from Chenopodium ambrosioides L. Braz. J. Microbiol. 2018 49 2 296 302 10.1016/j.bjm.2017.02.012 29037505
    [Google Scholar]
  23. Carneiro D.T.O. da Silva M.D. Vasconcelos K.V.P. Dias R. Costa V. Vasconcelos R.F. Carneiro B. Barreto G. Marques M. Vasconcelos H.C. Ribeiro Júnior H.L. Gusmão J.N.F.M. da Silveira H. Leitão R. Brito G.A. Pereira K.M.A. Gondim D.V. Goes P. Chenopodium ambrosioides Linn mitigates bone loss in rats with periodontitis. J. Dent. (Shiraz) 2024 25 1 59 67 38544779
    [Google Scholar]
  24. Drioua S. Ameggouz M. Assouguem A. Kara M. Ullah R. Bari A. Lahlali R. Fidan H. El-Guourrami O. Benkhouili F.Z. Maamar Y. Benzeid H. Doukkali A. Comprehensive phytochemical and toxicological analysis of Chenopodium ambrosioides (L.) fractions. Open Life Sci. 2024 19 1 20220895 10.1515/biol‑2022‑0895 38947765
    [Google Scholar]
  25. Soares M.H. Dias H.J. Vieira T.M. de Souza M.G.M. Cruz A.F.F. Badoco F.R. Nicolella H.D. Cunha W.R. Groppo M. Martins C.H.G. Tavares D.C. Magalhães L.G. Crotti A.E.M. Chemical composition, antibacterial, schistosomicidal, and cytotoxic activities of the essential oil of Dysphania ambrosioides (L.) mosyakin & clemants (chenopodiaceae). Chem. Biodivers. 2017 14 8 e1700149 10.1002/cbdv.201700149 28504841
    [Google Scholar]
  26. Reyes-Becerril M Angulo C Sanchez V. Vázquez-Martínez J. López M.G. Antioxidant, intestinal immune status, and anti-inflammatory potential of Chenopodium ambrosioides L. in fish: In vitro and in vivo studies. Fish Shellfish Immunol. 2019 86 420 428 10.1016/j.fsi.2018.11.059 30502468
    [Google Scholar]
  27. Boniface P. Kamto E. Paumo HK Katata-SeruL. Pegnyemb DE Ferreira E. Chemical constituents, ethnomedicinal uses, pharmacology, and toxicity of Dysphania ambrosioides (L.) Mosyakin & Clemants, formerly Chenopodium ambrosioides L. Nat. Prod. J. 2021 11 3 10.2174/2210315511666210920144526
    [Google Scholar]
  28. Calado G.P. Lopes A.J.O. Costa Junior L.M. Lima F.C.A. Silva L.A. Pereira W.S. Amaral F.M.M. Garcia J.B.S. Cartágenes M.S.S. Nascimento F.R.F. Chenopodium ambrosioides L. reduces synovial inflammation and pain in experimental osteoarthritis. PLoS One 2015 10 11 e0141886 10.1371/journal.pone.0141886 26524084
    [Google Scholar]
  29. Ribeiro R.M. De Brito Junior E.R. De Carvalho M.B.B. De Lima B.S.F. Andrade L.P. E Souza G.A.B.C. Moura J.C. Penha E.C.S. Dysphania ambrosioides: Phytochemical composition and pharmacological potential of the leaves. Brazilian J. Heal. Rev. 2023 6 4 18067 18084 10.34119/bjhrv6n4‑315
    [Google Scholar]
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