Department of Gynecology, Jinan Maternity and Child Care Hospital Affiliated to Shandong First Medical University, Jinan Maternity and Child Care Hospital, Jinan, China.
Eur Rev Med Pharmacol Sci. 2021 Sep;25(18):5610-5618. doi: 10.26355/eurrev_202109_26780.
This study aims to explore the biological roles of long non-coding RNA (lncRNA) ZNF281 and KLF15 in regulating cervical carcinoma progression.
Differential expressions of ZNF281 in 58 collected cervical carcinoma and normal tissues were detected by quantitative real-time polymerase chain reaction (qRT-PCR). The relationship between ZNF281 and clinicopathologic characteristics in cervical carcinoma patients was analyzed. By generating ZNF281 knockdown model in HeLa and SiHa cells through the transfection of shZNF281, migratory ability changes were examined via transwell and wound healing assay. The role of ZNF281 in in vivo tumorgenicity of cervical carcinoma was examined by implanting xenografted cancers in nude mice. The downstream target of ZNF281 and their interaction were assessed by bioinformatics tool and Dual-Luciferase reporter assay, respectively. Finally, co-regulations of ZNF281 and KLF15 on cervical carcinoma progression were elucidated.
ZNF281 was upregulated in cervical carcinoma tissues and cell lines. It was correlated to TNM staging, and incidences of lymphatic metastasis and distant metastasis in cervical carcinoma patients, while it was unrelated to age and tumor size. The knockdown of ZNF281 effectively attenuated migratory ability in HeLa and SiHa cells. Besides, knockdown of ZNF281 also reduced tumorigenicity of cervical carcinoma in nude mice. KLF15 was the downstream gene binding ZNF281, and they were negatively correlated to each other in cervical carcinoma tissues. Notably, KLF15 was responsible for ZNF281-induced regulation on cervical carcinoma migration.
LncRNA ZNF281 is upregulated in cervical carcinoma samples, and it is correlated to lymphatic metastasis, distant metastasis, and poor prognosis in cervical carcinoma patients. By targeting KLF15, ZNF281 triggers migratory potential in cervical carcinoma. We believed that ZNF281 is a promising biomarker for cervical carcinoma.
本研究旨在探讨长链非编码 RNA(lncRNA)ZNF281 和 KLF15 在调控宫颈癌进展中的生物学作用。
通过实时定量聚合酶链反应(qRT-PCR)检测 58 例收集的宫颈癌和正常组织中 ZNF281 的差异表达。分析 ZNF281 在宫颈癌患者临床病理特征中的相关性。通过转染 shZNF281 构建 ZNF281 敲低模型,在 HeLa 和 SiHa 细胞中进行转染,通过 Transwell 和划痕愈合实验检测迁移能力的变化。通过将异种移植的癌症植入裸鼠来检测 ZNF281 在体内宫颈癌致瘤性中的作用。通过生物信息学工具评估 ZNF281 的下游靶标及其相互作用,并分别通过双荧光素酶报告基因检测进行验证。最后,阐明 ZNF281 和 KLF15 对宫颈癌进展的共同调控作用。
ZNF281 在宫颈癌组织和细胞系中上调。它与宫颈癌患者的 TNM 分期、淋巴结转移和远处转移发生率相关,而与年龄和肿瘤大小无关。ZNF281 的敲低有效地减弱了 HeLa 和 SiHa 细胞的迁移能力。此外,ZNF281 的敲低还降低了裸鼠宫颈癌的致瘤性。KLF15 是与 ZNF281 结合的下游基因,它们在宫颈癌组织中呈负相关。值得注意的是,KLF15 负责 ZNF281 诱导的宫颈癌迁移调节。
lncRNA ZNF281 在宫颈癌样本中上调,与宫颈癌患者的淋巴结转移、远处转移和不良预后相关。通过靶向 KLF15,ZNF281 触发宫颈癌的迁移潜能。我们认为 ZNF281 是宫颈癌有前途的生物标志物。