首页|lncRNA SNHG6调控miR-1297表达对宫颈癌细胞生物学行为的影响

lncRNA SNHG6调控miR-1297表达对宫颈癌细胞生物学行为的影响

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目的 分析宫颈癌组织及细胞系中lncRNA SNHG6、miR-1297表达水平,探讨其与患者临床病理特征、宫颈癌细胞生物学行为的关系.方法 qRT-PCR检测90例宫颈癌组织、癌旁组织和人永生化宫颈上皮细胞(H8细胞)及宫颈癌细胞株中lncRNA SNHG6、miR-1297表达,分析宫颈癌组织中lncRNA SNHG6、miR-1297表达与临床病理指标的关系;将 HCC-94 细胞分为:control 组、si-NC 组、si-SNHG6 组、si-SNHG6+anti-miR-NC 组、si-SNHG6+anti-miR-1297组,qRT-PCR检测细胞中lncRNA SNHG6、miR-1297的表达;检测细胞增殖、迁移、侵袭和凋亡;Western blot方法检测增殖细胞核抗原(PCNA)、基质金属蛋白酶-2(MMP-2)、Bcl-2相关X蛋白(Bax)、细胞抗凋亡因子B淋巴细胞瘤-2(Bcl-2)蛋白的表达;双萤光素酶报告基因实验验证lncRNA SNHG6与miR-1297靶向调控关系.结果 在宫颈癌组织和细胞中,lncRNA SNHG6表达水平升高,miR-1297表达水平降低(P<0.05);临床分期≥Ⅲ期、低分化、有淋巴结转移的宫颈癌患者组织中lncRNA SNHG6表达水平升高、miR-1297表达水平降低(P<0.05);敲低lncRNA SNHG6表达可显著抑制HCC-94细胞增殖、迁移与侵袭,促进细胞凋亡(P<0.05);抑制miR-1297表达可逆转敲低lncRNA SNHG6表达对HCC-94细胞增殖、迁移、侵袭的抑制作用及对细胞凋亡的促进作用(P<0.05);双萤光素酶报告基因实验证实lncRNA SNHG6与miR-1297存在靶向调控关系.结论 在宫颈癌组织和细胞中lncRNA SNHG6上调表达,miR-1297下调表达,两者与肿瘤分期、组织分化程度和淋巴结转移密切相关,敲低lncRNA SNHG6可能通过上调miR-1297,抑制宫颈癌细胞增殖、迁移与侵袭,促进其凋亡.
The effect of lncRNA SNHG6 regulating miR-1297 expression on the biological behavior of cervical cancer cells
Objective To analyze the expression levels of lncRNA SNHG6 and miR-1297 in cervical cancer tissues and cell lines,and to explore their relationship with clinical pathological characteristics of patients and the biological behavior of cervical cancer cells.Methods qRT-PCR was used to detect the expression of lncRNA SNHG6 and miR-1297 in 90 cases of cervical cancer tissues,paracancerous tissues,human biological immortality cervical epithelial cells(H8 cells)and cervical cancer cell lines,the relationship between the expression of lncRNA SNHG6 and miR-1297 in cervical cancer tissue and clinical pathological indicators was analyzed.HCC-94 cells were divided into control group,si-NC group,si-SNHG6 group,si-SNHG6+anti-miR-NC group,and si-SNHG6+anti-miR-1297 group,qRT-PCR was applied to detect the expression of lncRNA SNHG6 and miR-1297 in cells.Cell proliferation,migration,invasion and apoptosis were detected.Western blot was applied to detect the expression of proliferating cell nuclear antigen(PCNA),matrix metalloproteinase-2(MMP-2),Bcl-2 associated X protein(Bax),and anti apoptosis factor B cell lymphoblastoma 2(Bcl-2)protein,and double luciferase reporter gene experiment was applied to verify the targeted regulation relationship between lncRNA SNHG6 and miR-1297.Results In cervical cancer tissues and cells,the expression level of lncRNA SNHG6 increased,while the expression level of miR-1297 decreased(P<0.05).The expression level of lncRNA SNHG6 increased and the expression level of miR-1297 decreased in tissues of cervical cancer patients with clinical stage ≥ Ⅲ,low differentiation,and lymph node metastasis(P<0.05).Knock-ing-down the expression of lncRNA SNHG6 was able to obviously inhibit the proliferation,migration,and invasion of HCC-94 cells,and promote cell apoptosis(P<0.05).Inhibiting the expression of miR-1297 was able to reverse the inhibitory effect of knocking down lncRNA SNHG6 expression on the proliferation,migration,and invasion of HCC-94 cells,and the promoting effect on cell apoptosis(P<0.05).The double luciferase reporter gene experiment confirmed that there was a tar-geted regulatory relationship between lncRNA SNHG6 and miR-1297.Conclusion lncRNA SNHG6 is up-regulated and miR-1297 is down-regulated in cervical cancer tissues and cells,they are closely related to tumor staging,tissue differentiation,and lymph node metastasis.Knocking-down lncRNA SNHG6 may up-regulate miR-1297 to inhibit the proliferation,migration,and invasion of cervical cancer cells,and promote their apoptosis.

cervical cancerlncRNA SNHG6/miR-1297proliferationmigration and invasionapoptosis

陈倩、伊碧霞、邵婷

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金华市人民医院妇产科,浙江金华 321000

宫颈癌 lncRNA SNHG6/miR-1297 增殖 迁移与侵袭 凋亡

2024

中国优生与遗传杂志
中国优生科学协会

中国优生与遗传杂志

CSTPCD
影响因子:0.527
ISSN:1006-9534
年,卷(期):2024.32(2)
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