Department of Thoracic Cardiovascular Surgery, The Eighth Affiliated Hospital of Sun Yat‑sen University, Shenzhen, Guangdong 518000, P.R. China.
Community Health Center, The Eighth Affiliated Hospital of Sun Yat‑sen University, Shenzhen, Guangdong 518000, P.R. China.
Oncol Rep. 2022 Dec;48(6). doi: 10.3892/or.2022.8434. Epub 2022 Oct 25.
Current investigations suggest that pigment epithelial‑derived factor (PEDF) can mediate the progression of non‑small cell lung cancer (NSCLC) by regulating autophagy. However, the underlying mechanisms associated with autophagy remain poorly elucidated. The aim of the present study was to investigate the association between the PEDF/adenosine 5'‑monophosphate‑activated protein kinase (AMPK)/Unc‑51 like autophagy‑activated kinase 1 (ULK1) pathway and autophagy in NSCLC. Intracellular autophagy was evaluated using indicators such as the expression and activation of microtubule‑associated protein light chain 3‑I (LC3‑I), LC3‑II and p62, as well as the distribution and number of autophagosomes observed by confocal microscopy. In addition, the activity and proliferative capacity of NSCLC cells under PEDF overexpression was also examined using Cell Counting Kit‑8 and lactate dehydrogenase (LDH) assays, and western blotting (WB) of related proteins. The results revealed that PEDF significantly inhibited NSCLC cell proliferation and viability, and increased LDH release and intercellular adhesion. Furthermore, PEDF suppressed the expression and activation of LC‑3 and reduced the number and distribution of autophagosomes. The PEDF‑induced inhibition of autophagy exhibited a direct association with the suppressed proliferation capacity and cell viability of NSCLC cells. The results of WB showed that NSCLC cells regulated autophagy through the AMPK/ULK1 signaling pathway. PEDF downregulated the AMPK/ULK1 signaling pathway, and AMPK or ULK1 overexpression markedly reduced the inhibitory effect of PEDF on autophagy. In conclusion, PEDF overexpression significantly inhibited the proliferative capacity and cell viability of NSCLC cells, as PEDF exerted an inhibitory function by regulating autophagy in NSCLC cells. Finally, it was demonstrated that autophagy may be suppressed by inhibiting the AMPK/ULK1 signaling pathway, thereby revealing a mechanism of lung cancer progression.
目前的研究表明,色素上皮衍生因子(PEDF)可通过调节自噬来介导非小细胞肺癌(NSCLC)的进展。然而,与自噬相关的潜在机制仍未得到充分阐明。本研究旨在探讨 PEDF/腺苷 5'-单磷酸激活蛋白激酶(AMPK)/UNC-51 样自噬激活激酶 1(ULK1)通路与 NSCLC 中自噬之间的关联。通过微管相关蛋白轻链 3-I(LC3-I)、LC3-II 和 p62 的表达和激活,以及通过共聚焦显微镜观察自噬体的分布和数量等指标来评估细胞内自噬。此外,还通过细胞计数试剂盒-8 和乳酸脱氢酶(LDH)测定以及相关蛋白的 Western blot(WB)检测 PEDF 过表达对 NSCLC 细胞活性和增殖能力的影响。结果显示,PEDF 可显著抑制 NSCLC 细胞增殖和活力,并增加 LDH 释放和细胞间黏附。此外,PEDF 抑制 LC-3 的表达和激活,并减少自噬体的数量和分布。PEDF 诱导的自噬抑制与 NSCLC 细胞增殖能力和细胞活力的抑制直接相关。WB 结果表明,NSCLC 细胞通过 AMPK/ULK1 信号通路调节自噬。PEDF 下调 AMPK/ULK1 信号通路,并且 AMPK 或 ULK1 的过表达显著降低了 PEDF 对自噬的抑制作用。综上所述,PEDF 过表达可显著抑制 NSCLC 细胞的增殖能力和细胞活力,因为 PEDF 通过调节 NSCLC 细胞中的自噬发挥抑制作用。最后,研究表明通过抑制 AMPK/ULK1 信号通路可抑制自噬,从而揭示了肺癌进展的一种机制。