Chen Qiuqiu, Pan Min, Lu Yusong, Wei Feifei, Chen Chunqiao, Huang Hui
Guilin People's Hospital, Guilin 541002, China.
J Oncol. 2022 Aug 11;2022:6925772. doi: 10.1155/2022/6925772. eCollection 2022.
Radix Actinidiae extract (RAE) has been shown to inhibit cancer in many studies, but its potential mechanism in nasopharyngeal cancer (NPC) progression remains unclear.
NPC cells (SUNE1) were treated with different doses of RAE. For transfection, SUNE1 cells were transfected with the microRNA (miR)-205-5p inhibitor (anti-miR-205-5p) or mimic followed by treatment with 200 g/mL RAE for 24 h. The MTT assay and colony formation assay were used to detect cell proliferation and radiosensitivity. The transwell assay was used to detect cell migration and invasion. The expression of miR-205-5p was detected by quantitative real-time PCR. The protein expression levels of matrix metalloproteinase-2 (MMP2) and matrix metalloproteinase-9 (MMP9) were detected by western blot analysis.
RAE inhibited NPC cell proliferation, migration, and invasion, while it enhanced radiosensitivity ( < 0.05). Also, RAE treatment decreased miR-205-5p expression, as well as MMP2 and MMP9 protein levels ( < 0.05). Anti-miR-205-5p transfection enhanced the effects of RAE on NPC cell proliferation, migration, invasion, and radiosensitivity ( < 0.05), while miR-205-5p mimic transfection had an opposite effect ( < 0.05).
RAE might decrease miR-205-5p, thereby it inhibited NPC cell proliferation and metastasis and enhanced radiosensitivity.
在许多研究中已表明猕猴桃根提取物(RAE)具有抗癌作用,但其在鼻咽癌(NPC)进展中的潜在机制仍不清楚。
用不同剂量的RAE处理NPC细胞(SUNE1)。对于转染,将SUNE1细胞用微小RNA(miR)-205-5p抑制剂(抗miR-205-5p)或模拟物转染,随后用200μg/mL RAE处理24小时。采用MTT法和集落形成试验检测细胞增殖和放射敏感性。采用Transwell试验检测细胞迁移和侵袭。通过定量实时PCR检测miR-205-5p的表达。通过蛋白质印迹分析检测基质金属蛋白酶-2(MMP2)和基质金属蛋白酶-9(MMP9)的蛋白表达水平。
RAE抑制NPC细胞增殖、迁移和侵袭,同时增强放射敏感性(P<0.05)。此外,RAE处理降低了miR-205-5p的表达以及MMP2和MMP9的蛋白水平(P<0.05)。抗miR-205-5p转染增强了RAE对NPC细胞增殖、迁移、侵袭和放射敏感性的影响(P<0.05),而miR-205-5p模拟物转染则产生相反的效果(P<0.05)。
RAE可能降低miR-205-5p,从而抑制NPC细胞增殖和转移并增强放射敏感性。