Journals / Gülhane Tıp Dergisi / 2015 / Cilt: 57 - Sayı: 3

Anti-angiogenic role of Ankaferd on chick chorioallontoic membrane model

Pages
274–279
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

Due to gene expression analyses resuts in our study, Ankaferd affects the angiogenesis in anti-angiogenic procedure on VEGF and HIF genes

📌 3 Key Takeaways

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Objective & Hypothesis:Angiogenesis is needed for tumor growth and metastasis.
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Key Findings & Data:Ankaferd was applied at 1, 5, 20, 50% concentrations to the fertilized eggs on the 6th day.
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Conclusion & Impact:Due to gene expression analyses resuts in our study, Ankaferd affects the angiogenesis in anti-angiogenic procedure on VEGF and HIF genes
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Angiogenesis is needed for tumor growth and metastasis. For this reason, it represents an exciting target for cancer treatment. Some anti-angiogenic drugs may be useful to prevent angiogenesis during cancer treatment. The aim of this study is to investigate if Ankaferd (standardized herbal extract obtained from five different plants namely Thymus vulgaris, Glycyrrhiza glabra, Vitis vinifera, Alpina officinarum, and Urtica dioica) have an effect on angiogenesis in chick embryo chorioallontoic membrane. Ankaferd was applied at 1, 5, 20, 50% concentrations to the fertilized eggs on the 6th day. On the 7th and 8th days, all the fertilized eggs were opened and vessels were examined. No significant changes were observed in 1% Ankaferd group and control group. Significant inhibition in angiogenesis was observed in 5, 20, 50% Ankaferd groups. In chick embryo chorioallontoic membrane assay, the anti-angiogenic effect of Ankaferd was shown experimentally for the first time in the literature. The antiangiogenic affect of Ancafert was analyzed on vascular endothelial growth factors (VEGF-A,VEGF-C), and hypoxia-inducible factors (HIF1-A and HIF3-A) genes which have possible roles in angiogenesis on human mesenchimal stem cells and human umbilical vein endothelial cells. Ankaferd treatment increased VEGF-A gene expression levels in HUVECs. VEGF-A gene expression levels remained unchanced in hMSCs with %5 Ankaferd treatment. HIF1-A gene expression levels decreased in HUVECs, whereas increased in hMSCs with 5% Ankaferd treatment. The gene expression levels of HIF3-A increased both in HUVECs and hMSCs. In chick embryo chorioallontoic membrane assay, the anti-angiogenic effect of Ankaferd was shown experimentally for the first time in the literature. These findings may represents the potential uses of Ankaferd in cancer treatment as an anti-angiogenic agent. Due to gene expression analyses resuts in our study, Ankaferd affects the angiogenesis in anti-angiogenic procedure on VEGF and HIF genes

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Cite This Article

GÜLŞEN, M. R., UZUNAY, N. S., FERMANLI, O., ÇOBAN, Z. D., ÖZTÜRK, D., HAMİDİ, M., AVCU, F., GÜRAN, Ş. (2015). Anti-angiogenic role of Ankaferd on chick chorioallontoic membrane model. Gülhane Tıp Dergisi, Cilt: 57 - Sayı: 3, 274–279. https://ajindex.com/articles/200415

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References (9)

  1. Z. Risau W. Mechanisms of angiogenesis. Nature 1997; 386:671-674. Shojaei F. Anti-angiogenesis therapy in cancer: Current challenges and future perspectives. Cancer Lett.2012; 320:130-137.
  2. Carmeliet P, Jain RK. Molecular mechanisms and clinical applications of angiogenesis. Nature.2011; 473:298-307.
  3. Said SS, Pickering JG, Mequanint K. Advances in growth factor delivery for therapeutic angiogenesis. J Vasc Res. 2013;50(1):35-51.
  4. Ataergin, A. S, Özet, A. Arpacı, F. Kanser Tedavisinde Anjiyogenez İnhibitörlerinin Yeri. Turkiye Klinikleri J Med Sci 1999;19(2):100-5.
  5. Beyazıt Y, Kurt M, Kekilli M, et al: Evaluation of hemosta- tic effects of Ankaferd as an alternative medicine. Altern Med Rev. 2010 Dec;15(4):329-36.
  6. Knighton D, Ausprunk D, Tapper D, et al: Avascular and vascular phases of tumour growth in the chick embryo. Br J Cancer 1977;35(3);347-356.
  7. Kurzen H, Schmitt S, Näher H, Möhler T. Inhibition of an- giogenesis by non-toxic doses of temozolomide. Antican- cer Drugs. 2003 Aug;14(7):515-22. Woltering EA. Development of targeted somatostatin-ba- sed antiangiogenic therapy: a review and future perspec- tives. Cancer Biother Radiopharm. 2003 Aug;18(4):601- 9. Cook D, Genever P. Regulation of mesenchymal stem cell differentiation. Adv Exp Med Biol. 2013;786:213-29. doi: 10.1007/978-94-007-6621-1_12. Wislet-Gendebien S, Wautier F, Leprince P, Rogister B.Astrocytic and neuronal fate of mesenchymal stem cells expressing nestin. Brain Res Bull. 2005 Dec 15;68(1-2):95-102.
  8. Katsuda T, Kosaka N, Takeshita F, Ochiya T. The thera- peutic potential of mesenchymal stem cell-derived extra- cellular vesicles. Proteomics. 2013 May;13(10-11):1637- 53. Karabıyık A, Yılmaz E, Güleç Ş, Haznedaroğlu İ, Akar N. Dual Diverse Dynamic Reversible Actions of Ankaferd on EPCR and PAI-1 Inside Vascular Endothelial Cells With and Without LPS. Turk J Hematol. Year: 2012 Volume: 29 Issue: 4 361-366 Özgürtaş T: Anjiyojenezde bir in-vivo model: civciv kori- yoallantoik membran. Gülhane Tıp Dergisi 2009; 51: 67- 69. Ramakrishnan A, Torok-Storb B, Pillai MM. Primary mar- row-derived stromal cells: isolation and manipulation. Methods Mol Biol. 2013;1035:75-101.
  9. Koyama H, Ikeda S, Sugimoto M, Kume S. Effects of Fo- lic Acid on the Development and Oxidative Stress of Mo- use Embryos Exposed to Heat Stress. Reprod Domest Anim. 2012 Feb 7. Kilicoglu B, Kismet K, Koru O, Tanyuksel M, Oruc MT, Sorkun K, Akkus MA. The scolicidal effects of honey. Adv Ther. 2006 Nov-Dec;23(6):1077-83. Claesson-Welsh