HL-7 肽在诱导 HeLa 癌细胞凋亡的内在信号途径中的作用

Zahra Setayesh-Mehr, Mohammad Hajitabar, Asghar Parsaei
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引用次数: 0

摘要

摘要-- 抗癌肽是治疗癌症的重要药物。目前,细胞凋亡过程被认为是癌症治疗的分子靶点。本研究采用 MTT 法研究了 HL-7 肽对宫颈癌细胞 HeLa 的毒性作用。此外,还通过实时 PCR 评估了经 HL-7 处理的 HeLa 细胞中 Bax、Bcl-2、p53、caspase-3、PTEN 和 Akt 基因的表达水平。此外,还使用流式细胞术测定了处于凋亡早期和晚期的细胞百分比。结果表明,多肽 HL-7 能抑制 HeLa 细胞的生长,IC50 为 31 μM。与未处理的 HeLa 细胞相比,经 HL-7 肽处理的 HeLa 细胞中 Bax、p53、caspase-3 和 PTEN 基因的表达水平升高,而 Bcl-2 和 Akt 基因的表达水平降低(p < 0.05)。流式细胞术分析结果表明,处于凋亡晚期的细胞比例较高(p <0.05)。我们的研究结果表明,肽 HL-7 可参与诱导线粒体依赖性细胞凋亡途径。然而,要阐明该肽对 HeLa 癌细胞的确切作用机制及其在临床上的治疗应用前景,还需要进行更多的研究。
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The Role of the HL-7 Peptide in the Induction of the Intrinsic Signalling Pathway of Apoptosis in HeLa Cancer Cells

Anticancer peptides are of interest for cancer treatment. Nowadays, the process of apoptosis is considered a molecular target for cancer therapy. In the present study, the toxic effect of the HL-7 peptide on cervical cancer cells HeLa was investigated using the MTT assay. Also, the expression levels of Bax, Bcl-2, p53, caspase-3, PTEN, and Akt genes in HeLa cells treated with HL-7 were assessed by real-time PCR. Besides, the percentage of cells in early and late stages of apoptosis was determined using flow cytometry. The obtained results indicated that the peptide HL-7 inhibited growth of HeLa cells with IC50 of 31 μM. The expression levels of Bax, p53, caspase-3, and PTEN genes were increased in HeLa cells treated with the HL-7 peptide as compared to untreated HeLa cells, while the expression levels of Bcl-2 and Akt genes was decreased (p < 0.05). The results of flow cytometry analysis indicated a high percentage of cells in the late apoptosis stage (p < 0.05). Our findings suggest that peptide HL-7 can be involved in inducing the mitochondria-dependent apoptosis pathway. However, additional studies are needed to elucidate the exact mechanism of action of the peptide on HeLa cancer cells and the prospects for its therapeutic use in the clinic.

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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
28
期刊介绍: Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology   is an international peer reviewed journal that publishes original articles on physical, chemical, and molecular mechanisms that underlie basic properties of biological membranes and mediate membrane-related cellular functions. The primary topics of the journal are membrane structure, mechanisms of membrane transport, bioenergetics and photobiology, intracellular signaling as well as membrane aspects of cell biology, immunology, and medicine. The journal is multidisciplinary and gives preference to those articles that employ a variety of experimental approaches, basically in biophysics but also in biochemistry, cytology, and molecular biology. The journal publishes articles that strive for unveiling membrane and cellular functions through innovative theoretical models and computer simulations.
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