Department of Internal Medicine, Taian Dongping County People's Hospital, Taian, China.
Eur Rev Med Pharmacol Sci. 2020 Jun;24(12):6818-6824. doi: 10.26355/eurrev_202006_21671.
To explore the expression of linc00324 in papillary thyroid cancer (PTC) and its effect on the biological function of PTC cells.
A total of 60 pairs of PTC and para-carcinoma normal tissues surgically excised were collected. The expression of linc00324 in PTC tissues and cells was detected via quantitative Reverse Transcription-Polymerase Chain Reaction (qRT-PCR), and the expression of linc00324 in PTC cells was silenced using the small-interfering RNA (siRNA). Then, the effects of linc00324 on the PTC cell proliferation, apoptosis, and cycle and the downstream Notch signaling pathway were determined via methyl thiazolyl tetrazolium (MTT) assay, colony formation assay, flow cytometry, and Western blotting, respectively.
The expression of linc00324 was upregulated in 48 out of 60 cases of PTC tissues, and it was increased in PTC cells compared with that in human thyroid follicular epithelial cells Nthy-ori 3-1. The results of MTT assay and colony formation assay showed that the proliferation of PTC cells declined after interference in linc00324 expression. The findings of flow cytometry revealed that the cell cycle was arrested in G1/G0 phase with a higher apoptosis rate in si-linc00324 group compared with that in the si-NC group. According to the data of Western blotting, the molecular markers for the downstream Notch signaling pathway were altered after interference in linc00324 expression.
The expression of linc00324 is significantly increased in PTC tissues and cells. Silencing linc00324 may inhibit the proliferation of PTC cells, arrest the cell cycle in G1/G0 phase, and promote the apoptosis by inhibiting the Notch signaling pathway.
探讨 linc00324 在甲状腺乳头状癌(PTC)中的表达及其对 PTC 细胞生物学功能的影响。
收集 60 对手术切除的 PTC 及癌旁正常组织,采用实时定量逆转录聚合酶链反应(qRT-PCR)检测 linc00324 在 PTC 组织和细胞中的表达,采用小干扰 RNA(siRNA)沉默 PTC 细胞中的 linc00324 表达。然后,通过噻唑蓝(MTT)比色法、集落形成实验、流式细胞术和 Western blot 分别检测 linc00324 对 PTC 细胞增殖、凋亡、细胞周期及下游 Notch 信号通路的影响。
60 例 PTC 组织中,有 48 例 linc00324 表达上调,PTC 细胞中 linc00324 的表达高于人甲状腺滤泡上皮细胞 Nthy-ori 3-1。MTT 比色法和集落形成实验结果表明,干扰 linc00324 表达后 PTC 细胞增殖能力下降。流式细胞术结果显示,si-linc00324 组细胞周期阻滞于 G1/G0 期,凋亡率高于 si-NC 组。Western blot 结果显示,干扰 linc00324 表达后,下游 Notch 信号通路的分子标志物发生改变。
linc00324 在 PTC 组织和细胞中表达显著上调。沉默 linc00324 可能通过抑制 Notch 信号通路抑制 PTC 细胞增殖,阻滞细胞周期于 G1/G0 期,促进细胞凋亡。