Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou, China.
Life Science and Engineering College of Northwest Minzu University, Lanzhou, China.
Cell Biochem Funct. 2023 Dec;41(8):1395-1402. doi: 10.1002/cbf.3873. Epub 2023 Oct 16.
Cervical cancer is one of the foremost common cancers in women. Lactoferrin (LF) has many biological functions, such as antitumor. This study aimed to explore the regulatory effect of bovine lactoferrin (bLF) on the proliferation and apoptosis of cervical cancer HeLa cells and to clarify the potential mechanism of action of bLF against HeLa cells. This study used CCK-8, Trypan blue staining, and colony formation assays to verify the effect of bLF on HeLa cell proliferation. Hoechst 33258 fluorescence staining, AO/EB staining, and western blotting were used to determine the effects of bLF on apoptosis and autophagy in HeLa cells. We discovered that bLF significantly reduced the proliferation of HeLa cells in a dose- and time-dependent manner compared to the control group. Furthermore, bLF primarily induced apoptosis in HeLa cells by increasing the expression of the proapoptotic proteins p53, Bax, and Cleaved-caspase-3 and downregulating the expression of the antiapoptotic protein Bcl-2. In addition, the present study also showed that bLF treatment significantly activated autophagy-related proteins LC3B-II and Beclin I and down regulated the autophagosome transporter protein p62, indicating that bLF treatment can induce autophagy in HeLa cells. After pretreatment with the autophagy inhibitor, 3-MA, which markedly found that autophagy inhibition by 3-MA reversed bLF-induced apoptosis, indicating that bLF can induce apoptosis by activating intracellular autophagy in HeLa cells. In the present study, our results support the theory of bLF significantly inhibited the proliferation of Hela cells by promoting apoptosis and reinforcing autophagy. The study will play an important role in therapying cervical cancer.
宫颈癌是女性中最常见的癌症之一。乳铁蛋白 (LF) 具有多种生物学功能,如抗肿瘤。本研究旨在探讨牛乳铁蛋白 (bLF) 对宫颈癌 HeLa 细胞增殖和凋亡的调节作用,并阐明 bLF 对 HeLa 细胞作用的潜在机制。本研究采用 CCK-8、台盼蓝染色和集落形成实验验证 bLF 对 HeLa 细胞增殖的影响。采用 Hoechst 33258 荧光染色、AO/EB 染色和 Western blot 检测 bLF 对 HeLa 细胞凋亡和自噬的影响。结果发现,bLF 显著降低 HeLa 细胞的增殖,呈剂量和时间依赖性。此外,bLF 主要通过增加促凋亡蛋白 p53、Bax 和 Cleaved-caspase-3 的表达,下调抗凋亡蛋白 Bcl-2 的表达,诱导 HeLa 细胞凋亡。此外,本研究还表明,bLF 处理可显著激活自噬相关蛋白 LC3B-II 和 Beclin I,并下调自噬体转运蛋白 p62,表明 bLF 处理可诱导 HeLa 细胞发生自噬。用自噬抑制剂 3-MA 预处理后,发现自噬抑制剂 3-MA 明显逆转了 bLF 诱导的凋亡,表明 bLF 可通过激活 HeLa 细胞内的自噬来诱导凋亡。本研究结果支持 bLF 通过促进凋亡和增强自噬显著抑制 Hela 细胞增殖的理论。该研究将在宫颈癌治疗中发挥重要作用。