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Investigation of the effect of rhamnetin on mice injected with solid and ehrlich ascites tumor

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Abstract

Rhamnetin is a flavonoid which contained in especially clove, such as apple, tea, and onion plant. Rhamnetin has been used in cancer research due to its antitumor and antioxidant properties. In this study, effects of rhamnetin administration at different doses on ascites and solid tumors were investigated in Balb/C mice bearing EAT model that originating from rat breast adenocarcinoma. Experimental procedure: Overall, 92 Balb-c mice were used in this study. EAT cells (1 × 106 cells) that harvested from stock animals were injected to all rats via intraperitoneal and subcutaneous route. Rhamnetin (100 µg/kg–200 µg/kg) were given intraperitoneally and subcutaneously during 10 and 15 days to the animals bearing ascites tumor and solid tumor, respectively. Throughout experiments, weight changes were recorded in all groups. The maximum weight increase was observed in the control group among all groups (ascites and solid tumor groups). In the treatment groups, the least weight increase were determined in 200-µg/kg rhamnetin applied. The lowest increase in tumor volume was observed in the group that received 200-µg/kg rhamnetin (2.84) when compared to tumor control group (3.67). Result and conclusion: We determined that the number of live and dead cells in the treatment groups administered with the mean rhamnetin dose (2.5 µg/ml) was found in the count made in the EAT cell line after the incubation periods. We observed that rhamnetin plays an important role against cancer formation. We have obtained important results in our study, but detailed studies on the relationship between rhamnetin and cancer are needed.

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Data sharing not applicable to this article as no datasets were generated or analysed during the current study.

Abbreviations

µg:

Microgram

µl:

Microliter

cm:

Centimeter

kg:

Kilogram

g:

Gram

mg:

Milligram

h:

Hour

DAB:

Diaminobenzidine

DAPI:

4,6-Diamidino-2-phenylindole

TdT:

Terminal deoxynucleotidyl transferase

dUTP:

Nonisotopic labeled nucleotides

TUNEL:

Terminal deoxynucleotidyl transferase-mediated dUTP Nick-end Labeling

EAT:

Ehrlich Ascites Tumor

PS:

Physiological saline

FITCH:

Fluorescein isothiocyanate

FVIII:

Factor VIII

ml:

Milliliter

mm3 :

Cubic millimeter

NSCLC:

Non-small cell lung cancer cells

PBS:

Phosphate buffer saline

DNA:

Deoxyribonucleic acid

W:

Watt

ip:

Intraperitoneal

sc:

Subcutaneous

References

  1. Imran M, Rauf A, Izneid TA, et al. Luteolin, a flavonoid, as an anticancer agent: A review. Biomed Pharmacother. 2019;112:108612. https://doi.org/10.1016/j.biopha.2019.108612.

    Article  CAS  PubMed  Google Scholar 

  2. Srivastava S, Somasagara RR, Hegde M, et al. Quercetin, a natural flavonoid interacts with DNA, arrests cell cycle and causes tumor regression by activating mitochondrial pathway of apoptosis. Sci Rep. 2016;6:24049.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. WHO Report On Cancer Settıng Priorities, Investiıng Wisely And Providing Care For All;2020. Chapter 01, The Growing Burden Of Cancer P.13

  4. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2020. Ca Cancer J Clin. 2020;70:7–30.

    Article  PubMed  Google Scholar 

  5. Raju A, Christina MJA, Murali A. Antitumor activity of ethanol and aqueous extracts of Drosera Burmannii Vahl. EAC bearing mice Spatula DD. 2012;2:83–8.

    Article  Google Scholar 

  6. Tavsan Z, Kayali HA. Flavonoids showed anticancer effects on the ovarian cancer cells: Involvement of reactive oxygen species, apoptosis, cell cycle and invasion. Biomed Pharmacother. 2019;116:109004.

    Article  CAS  PubMed  Google Scholar 

  7. Yılmaz S, Ülger H, Ertekin T, et al. Investigating the anti-tumoral effect of curcumin on the mice in which Ehrlich ascites and solid tumor is created. Iran J Basic Med Sci. 2019;22(4):418–25.

    PubMed  PubMed Central  Google Scholar 

  8. Youns M, Halim Hegazy WA. The Natural flavonoid fisetin inhibits cellular proliferation of hepatic, colorectal, and pancreatic cancer cells through modulation of multiple signaling pathways. PLoS ONE. 2017;12(1):e0169335.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Lee KP, Kim JE, Park WH. Cytoprotective effect of rhamnetin on miconazoleinduced H9c2 cell damage. Nutr Res Pract. 2015;9:586–91.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Babasaheb PB, Shrikant SG, Ragini GB, et al. Synthesis and biological evaluation of simple methoxylated chalcones as anticancer, anti-infl ammatory and antioxidant agents. Bioorg Med Chem. 2010;18:1364–70.

    Article  Google Scholar 

  11. Varmus H. The new era in cancer research. Science. 2006;26:1162–5.

    Article  Google Scholar 

  12. Tozkoparan B, Aytaç SP. As a therapeutic target in cancer chemotherapy, glutathione S-transferases. J Fac Pharm. 2007;27:139–64.

    CAS  Google Scholar 

  13. Kızılcı S. Factors affecting the quality of life of cancer patients and their relatives receiving chemotherapy. J Nurs. 1999;3:18–26.

    Google Scholar 

  14. Videira M, Reis RL, Brito MA. Deconstructing breast cancer cell biology and the mechanisms of multidrug resistance. Biochim Biophys Acta. 2014;1846:312–25.

    CAS  PubMed  Google Scholar 

  15. Zeybek Ü. Cancer research and experimental models. J Exp Med Res Ins. 2013;3:187–98.

    Google Scholar 

  16. Tsaı PH, Cheng CH, Lın CY, et al. Dietary flavonoids luteolin and quercetin suppressed cancer stem cell properties and metastatic potential of isolated prostate cancer cells. Anticancer Res. 2016;36(12):6367–80.

    Article  PubMed  Google Scholar 

  17. Kim YJ. Rhamnetin attenuates melanogenesis by suppressing oxidative stress and pro-inflammatory mediators. Biol Pharm Bull. 2013;36(8):1341–7.

    Article  CAS  PubMed  Google Scholar 

  18. Kang JH, Kim EG, Kim W, et al. Rhamnetin and cirsiliol induce radiosensitization and inhibition of epithelial-mesenchymal transition (EMT) by miR-34a-mediated suppression of notch-1 expression in non-small cell lung cancer cell lines. J Biol Chem. 2013;288(38):27343–57.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Lan L, Wang Y, Pan Z, et al. Rhamnetin induces apoptosis in human breast cancer cells via the miR-34a/Notch-1 signaling pathway. Oncol Lett. 2019;17(1):676–82.

    CAS  PubMed  Google Scholar 

  20. Hlatky L, Hahnfeldt P, Folkman J. Clinical application of antiangiogenic therapy: microvessel density, what it does and doesn’t tell us. J Natl Cancer Inst. 2002;94:883–93.

    Article  PubMed  Google Scholar 

  21. Yılmaz H, Ertekin T, Atay E, et al. Antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development. Iran J Basic Med Sci. 2018;21:787–93.

    PubMed  PubMed Central  Google Scholar 

  22. Delisser HM. Involvement of endothelial PECAM-1/CD31 in angiogenesis. Am J Pathol. 1997;151:671–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  23. Yokozawa T, Kim YJ. Piceatannol inhibits melanogenesis by its antioxidative actions. Biol Pharm Bull. 2007;30(11):2007–11. https://doi.org/10.1248/bpb.30.2007.

    Article  CAS  PubMed  Google Scholar 

  24. Kim YJ, Kang KS, Yokozawa T. The anti-melanogenic effect of pycnogenol by its anti-oxidative actions. Food Chem Toxicol. 2008;46(7):2466–71. https://doi.org/10.1016/j.fct.2008.04.002.

    Article  CAS  PubMed  Google Scholar 

  25. Kim YJ. Antimelanogenic and antioxidant properties of gallic acid. Biol Pharm Bull. 2007;30(6):1052–5. https://doi.org/10.1248/bpb.30.1052.

    Article  CAS  PubMed  Google Scholar 

  26. Chung SW, Ha YM, Kim YJ, et al. Inhibitory effects of 6-(3-hydroxyphenyl)-2-naphthol on tyrosinase activity and melanin synthesis. Arch Pharm Res. 2009;32(2):289–94. https://doi.org/10.1007/s12272-009-1235-9.

    Article  CAS  PubMed  Google Scholar 

  27. Panich U, Onkoksoong T, Limsaengurai S, et al. UVA-induced melanogenesis and modulation of glutathione redox system in different melanoma cell lines: the protective effect of gallic acid. J Photochem Photobiol B. 2012;1(108):16–22. https://doi.org/10.1016/j.jphotobiol.2011.12.004.

    Article  CAS  Google Scholar 

  28. Bağcı Uzun G, Nisari M, Hanım Yay A, et al. Investigating the anti-tumoral effect of yarrow (Achillea milllefolium) on the mice in which ehrlich solid tumor is created. Med Oncol. 2023;40:42. https://doi.org/10.1007/s12032-022-01917-3.

    Article  CAS  Google Scholar 

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Acknowledgements

This research was produced from Özlem Bozkurt’s PhD thesis named “The investigating the antitumoral effect of rhamnetin on the mice,” in which Ehrlich ascites and solid tumor is created. Financial source of this research was funded by Erciyes University Scientific Research Projects Coordination Unit.

Funding

Bilimsel Araştırma Projeleri, Erciyes Üniversitesi, TDK-2014-5247, Erdoğan Unur

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Bozkurt, Ö., Yılmaz, S., Alpa, Ş. et al. Investigation of the effect of rhamnetin on mice injected with solid and ehrlich ascites tumor. Med Oncol 40, 124 (2023). https://doi.org/10.1007/s12032-023-01981-3

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