Determination Of Inhibitory Effects of Newly Synthesized Potential HIF Inhibitors on Non-Small Cell Lung Cancer Under Hypoxic Conditions

D. Kahraman, Pınar Yumrutaş, Esra Bozgeyik, I. Bozgeyik, A. İyi̇doğan, E. E. Oruç-Emre, Serdar Öztuzcu, Ahmet Ferudun Işik
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Abstract

According to global estimates, there are 2.3 million new cases and 1.8 million fatalities due to lung cancer each year. Despite recent progress in diagnosis and treatment, persistent challenges highlight the urgent need for novel therapeutics and innovative approaches to combat lung cancer effectively. Accordingly, in the present study, we aimed to investigate the anticancer properties of potential inhibitors of HIF-1α, compound 7a and 7b. In the study, HTB-54 and BEAS-2B cell lines were used. MTT cell viability experiments were performed to determine the effect of newly synthesized HIF inhibitors 7a and 7b on cell viability under normoxic and hypoxic conditions. Quantitative expression levels of HIF1A were determined by real-time PCR approach. While the half maximum inhibitory concentration (IC50) of compound 7a in HTB-54 cells was 10.37 µM under normoxic conditions, it was found to be 10.63 µM under hypoxic conditions. The IC50 value of another HIF inhibitor 7b in HTB-54 cells was found to be 8.80 µM under normoxic conditions and 9.54 µM under hypoxic conditions. The expression level of HIF1A was found to be lower in cells exposed to compounds 7a and 7b under hypoxia compared to the control group. Conversely, in normoxia, HIF1A expression level in cells exposed to compound 7a increased 6.5-fold compared to the control group, while it was found to increase approximately 9-fold when exposed to 7b. Consequently, both compound 7a and 7b holds great promise for future therapeutic interventions to lung cancer.
确定新合成的潜在 HIF 抑制剂在缺氧条件下对非小细胞肺癌的抑制作用
据全球估计,每年有 230 万新发病例和 180 万人死于肺癌。尽管最近在诊断和治疗方面取得了进展,但持续存在的挑战凸显出迫切需要新型疗法和创新方法来有效防治肺癌。因此,在本研究中,我们旨在研究潜在的 HIF-1α 抑制剂--化合物 7a 和 7b 的抗癌特性。本研究使用了 HTB-54 和 BEAS-2B 细胞系。进行了 MTT 细胞活力实验,以确定新合成的 HIF 抑制剂 7a 和 7b 在常氧和缺氧条件下对细胞活力的影响。实时 PCR 方法测定了 HIF1A 的定量表达水平。在常氧条件下,化合物 7a 在 HTB-54 细胞中的半数最大抑制浓度(IC50)为 10.37 µM,而在缺氧条件下则为 10.63 µM。另一种 HIF 抑制剂 7b 在 HTB-54 细胞中的 IC50 值在正常缺氧条件下为 8.80 µM,在缺氧条件下为 9.54 µM。与对照组相比,在缺氧条件下暴露于化合物 7a 和 7b 的细胞中,HIF1A 的表达水平较低。相反,在常氧条件下,暴露于化合物 7a 的细胞的 HIF1A 表达水平比对照组增加了 6.5 倍,而暴露于化合物 7b 的细胞的 HIF1A 表达水平增加了约 9 倍。因此,化合物 7a 和 7b 在未来干预肺癌治疗方面都大有可为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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