LncRNA SNHG17 Contributes to the Progression of Cervical Cancer by Targeting microRNA-375-3p

被引:17
作者
Cao, Shuping [1 ]
Li, Hongxia [2 ]
Li, Lei [3 ]
机构
[1] Dongying Dist Peoples Hosp, Dept Gynecol, Dongying, Shandong, Peoples R China
[2] Dongying Dist Peoples Hosp, Dept Obstet, Dongying, Shandong, Peoples R China
[3] Dongying Dist Peoples Hosp, Dept Pathol, 333 Jinan Rd, Dongying 257000, Shandong, Peoples R China
关键词
lncRNA SNHG17; miR-375-3p; clinical significance; biological function; cervical cancer; ADENOCARCINOMA PROGRESSION; OVARIAN-CANCER; BREAST-CANCER; PROLIFERATION; PROMOTES; DIAGNOSIS; CELLS; MIRNA; EXPRESSION; INVASION;
D O I
10.2147/CMAR.S312469
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Cervical cancer is a great threat to women's health all over the world. Non-coding RNAs performed a wide range of functions. This study aimed to clarify the clinical significance and biological function of lncRNA SNHG17 and miRNA-375-3p (miR-375-3p) in cervical cancer (CC). Patients and Methods: Blood samples from 124 CC patients and 119 healthy volunteers were collected. The relative expression of SNHG17 and miR-375-3p in CC patient serums and cells was evaluated by quantitative real-time polymerase chain reaction (qRT-PCR). The receiver operating curve (ROC) was plotted for diagnostic value estimation. The CCK-8 and transwell assay were conducted to explore the function of SNHG17 on CC cells. A luciferase reporter assay was carried out to confirm the interaction of SNHG17 and miR-375-3p. Rescue experiments were performed to verify the interaction. Results: SNHG17 showed an ascending expression while miR-375-3p descended in the serum of CC patients. For SNHG17 and miR-375-3p, respectively, the AUC was 0.863 and 0.869, the sensitivity was 84.7% and 75.8%, and the specificity was 78.2% and 86.6%. Knockdown of SNHG17 inhibited proliferation, migration, and invasion of CC cells. Serum SNHG17 expression was negatively correlated with miR-375-3p expression, and miR-375-3p was the target miRNA of SNHG17. Rescue experiments verified the knockdown of SNHG17 inhibited cell growth through repressing miR-375-3p expression. Conclusion: SNHG17 and miR-375-3p have the potential to be diagnostic markers for CC. Overexpression of SNHG17 in CC promoted the progression of CC partly via targeting miR-375-3p, implying a novel therapeutic target for CC emerging.
引用
收藏
页码:4969 / 4978
页数:10
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