Department of Oncology, The First People's Hospital of Qujing/The Qujing Affiliated Hospital of Kunming Medical University, Qujing, China.
Department of Pulmonary, The First People's Hospital of Qujing/The Qujing Affiliated Hospital of Kunming Medical University, Qujing, China.
J Cancer Res Ther. 2024 Aug 1;20(4):1284-1292. doi: 10.4103/jcrt.jcrt_1941_23. Epub 2024 Aug 29.
Radiation therapy is a crucial treatment for nonsmall cell lung cancer (NSCLC), but its effectiveness is limited by the resistance of tumor cells to radiation. This study aimed to evaluate the effect of epicatechin (EC) on radiosensitivity in NSCLC and to determine its relationships with matrix metalloproteinase (MMP)-9.
MMP-9 expression was detected by Western blotting, and the expression of the DNA damage marker protein was detected by immunofluorescence. Cell viability was assessed using the CCK-8 assay, and cell proliferation was evaluated using the clonogenesis assay. Flow cytometry was used to determine the cell apoptosis, whereas cell migration and invasion were detected using the transwell assays. The cells were treated with ionizing radiation (IR) and EC to verify the sensitizing effect of EC on radiation therapy.
MMP-9 expression was elevated in the NSCLC cells and tissues. DNA damage and cell apoptosis were increased, whereas cell vigor, proliferation, migration, and invasion were significantly decreased after IR. MMP-9 knockdown strengthened the impact of IR on the biological behaviors of the cells. EC + IR had the best effect on promoting DNA damage and the biological behaviors of the NSCLC cells; alternatively, the overexpression of MMP-9 weakened the role of EC.
This study shows that EC can downregulate MMP-9 expression, promote DNA damage, reduce cell viability, proliferation, migration, and invasion, and facilitate cell apoptosis, thus, showing potential as a radiosensitizer for NSCLC.
放射治疗是治疗非小细胞肺癌(NSCLC)的重要手段,但肿瘤细胞对放射治疗的抵抗限制了其疗效。本研究旨在评估表儿茶素(EC)对 NSCLC 放射敏感性的影响,并确定其与基质金属蛋白酶(MMP)-9 的关系。
采用 Western blot 检测 MMP-9 表达,免疫荧光检测 DNA 损伤标志物蛋白表达。采用 CCK-8 法评估细胞活力,克隆形成实验评估细胞增殖。采用流式细胞术检测细胞凋亡,Transwell 实验检测细胞迁移和侵袭。用电离辐射(IR)和 EC 处理细胞,验证 EC 对放射治疗的增敏作用。
MMP-9 在 NSCLC 细胞和组织中表达上调。IR 后 DNA 损伤和细胞凋亡增加,而细胞活力、增殖、迁移和侵袭显著降低。MMP-9 敲低增强了 IR 对细胞生物学行为的影响。EC+IR 对促进 NSCLC 细胞的 DNA 损伤和生物学行为效果最佳;相反,MMP-9 的过表达削弱了 EC 的作用。
本研究表明,EC 可下调 MMP-9 表达,促进 DNA 损伤,降低细胞活力、增殖、迁移和侵袭,促进细胞凋亡,因此具有作为 NSCLC 放射增敏剂的潜力。