Araştırma Makalesi

Investigation of The Effect of Compound B-47/2 Containing Azomethine Group On Angiogenesis

Cilt: 44 Sayı: 4 31 Aralık 2022
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Investigation of The Effect of Compound B-47/2 Containing Azomethine Group On Angiogenesis

Abstract

Objective: Lung cancer is one of the most common cancers in the world. It is known that angiogenesis plays a role in the development and metastasis of lung cancer. Azomethine derivatives known as Schiff bases have many biological activities. In this study, we aimed to determine the anticancer activity of the newly synthesized azomethine derivative compound B-47/2 on lung cancer and to determine the effect of this component on vascular endothelial growth factor B (VEGFB) gene expression. Material and Method: Compound B-47/2 was synthesized for the first time. B-47/2 compound was applied to lung cancer cell line (A549) at varying concentrations (1-100 µg/mL) and its anticancer activity was found after 24, 48 and 72 hours incubations using the 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) method. The half maximal inhibitory concentration (IC50) dose of B-47/2 was applied to the cells and ribonucleic acid (RNA) isolation followed by complementary deoxyribonucleic acid (cDNA) synthesis was performed. Then, reverse transcription-polymerase chain reaction (RT-PCR) method was used to determine the expression level of VEGFB gene. Results: As a result, it was determined that the B-47/2 compound applied to the A-549 cell line showed the highest cytotoxic activity after 72 hours of incubation. In addition, it was determined that the B-47/2 compound decreased the expression of the VEGFB gene. Discussion: There are studies in which the anticancer activity of azomethine derivatives has been observed. The topic of synthesizing new drugs to prevent cancer is popular. We suggested that the newly synthesized component may have anticancer activity and may be effective on angiogenesis.

Keywords

Kaynakça

  1. 1. Teleanu, R.I., et al., Tumor angiogenesis and anti-angiogenic strategies for cancer treatment. 2019. 9(1): p. 84.
  2. 2. Folkman, J.J.N.e.j.o.m., Tumor angiogenesis: therapeutic implications. 1971. 285(21): p. 1182-1186.
  3. 3. Ayoub, N.M., et al., Targeting Angiogenesis in Breast Cancer: Current Evidence and Future Perspectives of Novel Anti-Angiogenic Approaches. 2022. 13.
  4. 4. Lugano, R., et al., Tumor angiogenesis: causes, consequences, challenges and opportunities. 2020. 77(9): p. 1745-1770.
  5. 5. Liu, G., et al., Vascular endothelial growth factor B coordinates metastasis of non-small cell lung cancer. 2015. 36(3): p. 2185-2191.
  6. 6. Zhao, Y. and A.A.J.T.o. Adjei, Targeting angiogenesis in cancer therapy: moving beyond vascular endothelial growth factor. 2015. 20(6): p. 660-673.
  7. 7. Hu, H., et al., The research progress of antiangiogenic therapy, immune therapy and tumor microenvironment. 2022. 13: p. 802846.
  8. 8. Das, M. and H.J.E.o.o.t.t. Wakelee, Targeting VEGF in lung cancer. 2012. 16(4): p. 395-406.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Sağlık Kurumları Yönetimi

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

31 Aralık 2022

Gönderilme Tarihi

15 Ekim 2022

Kabul Tarihi

19 Aralık 2022

Yayımlandığı Sayı

Yıl 2022 Cilt: 44 Sayı: 4

Kaynak Göster

AMA
1.Bucak ET, Tunçbilek Z, Huseynzada A, vd. Investigation of The Effect of Compound B-47/2 Containing Azomethine Group On Angiogenesis. CMJ. 2022;44(4):343-347. doi:10.7197/cmj.1189799