Li Lili, Fan Jiangtao, Li Dahai, Liu Yan, Shrestha Poonam, Zhong Chunyan, Xia Xiuhong, Huang Xiaobing
Department of Gynecology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, P.R. China.
Oncol Lett. 2018 Aug;16(2):1777-1784. doi: 10.3892/ol.2018.8814. Epub 2018 May 25.
The present study aimed to investigate the effects of chitinase-3-like protein 1 (YKL-40) gene RNA interference on the biological behaviors and enhanced chemosensitivity of endometrial cancer (EC) HEC-1A cells. YKL-40 small interfering (si)RNA was transduced into EC HEC-1A cells using a lentivirus. The experiment was divided into three groups: The experimental group was transfected with YKL-40 siRNA (si-YKL-40); the mock-treatment group was transfected with transfection reagent only; and the blank control group was left untreated. A reverse transcription-quantitative polymerase chain reaction was performed to investigate the mRNA expression levels of YKL-40. The biological behaviors, including cell proliferation, migration, invasion and apoptosis, were detected by MTT and Transwell assays, and flow cytometry (FCM) analysis, respectively. The results of the present study demonstrated that the mRNA expression levels of YKL-40 were downregulated within HEC-1A cells upon transfection with si-YKL-40 (P<0.05). The proliferative, migratory and invasive abilities of HEC-1A cells were inhibited by si-YKL-40 (P<0.05). The mRNA expression levels of YKL-40 were upregulated within HEC-1A cells following treatment with cisplatin (P<0.05). FCM analysis revealed that the average cellular apoptosis rate increased following the inhibition of YKL-40 gene expression via siRNA (P<0.05). Therefore, the YKL-40 gene may be associated with the proliferative, migratory, invasive and anti-apoptotic ability of HEC-1A cells. YKL-40 downregulation may enhance the sensitivity of human EC HEC-1A cells to chemotherapy.
本研究旨在探讨几丁质酶-3样蛋白1(YKL-40)基因RNA干扰对子宫内膜癌(EC)HEC-1A细胞生物学行为及化疗敏感性增强的影响。使用慢病毒将YKL-40小干扰(si)RNA转导至EC HEC-1A细胞中。实验分为三组:实验组转染YKL-40 siRNA(si-YKL-40);模拟治疗组仅转染转染试剂;空白对照组不做处理。采用逆转录定量聚合酶链反应检测YKL-40的mRNA表达水平。分别通过MTT法、Transwell实验和流式细胞术(FCM)分析检测细胞增殖、迁移、侵袭和凋亡等生物学行为。本研究结果表明,转染si-YKL-40后,HEC-1A细胞内YKL-40的mRNA表达水平下调(P<0.05)。si-YKL-40抑制了HEC-1A细胞的增殖、迁移和侵袭能力(P<0.05)。顺铂处理后,HEC-1A细胞内YKL-40的mRNA表达水平上调(P<0.05)。FCM分析显示,通过siRNA抑制YKL-40基因表达后,细胞平均凋亡率增加(P<0.05)。因此,YKL-40基因可能与HEC-1A细胞的增殖、迁移、侵袭及抗凋亡能力有关。下调YKL-40可能增强人EC HEC-1A细胞对化疗的敏感性。