MiR-223-3p promotes cell proliferation and metastasis by downregulating SLC4A4 in clear cell renal cell carcinoma

被引:71
|
作者
Xiao, Wen [1 ,2 ,3 ]
Wang, Xuegang [1 ,2 ,3 ]
Wang, Tao [1 ,2 ,3 ]
Xing, Jinchun [1 ,2 ,3 ]
机构
[1] Xiamen Univ, Dept Urol, Affiliated Hosp 1, Xiamen, Fujian, Peoples R China
[2] Xiamen Univ, Ctr Diag & Treatment Urinary Syst Dis, Affiliated Hosp 1, Xiamen, Fujian, Peoples R China
[3] Xiamen Univ, Key Lab Urinary Tract Tumors & Calculi Xiamen Cit, Affiliated Hosp 1, Xiamen, Fujian, Peoples R China
来源
AGING-US | 2019年 / 11卷 / 02期
关键词
miR-223-3p; ccRCC; oncomiRNA; SLC4A4; metastasis; CANCER; INVASION; EXPRESSION; CONTRIBUTES; BIOGENESIS; MANAGEMENT; MICRORNAS; MIGRATION; GENOMICS;
D O I
10.18632/aging.101763
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MicroRNAs (miRNAs) are known to affect the occurrence and progression of cancer. We therefore evaluated the involvement of miR-223-3p in renal cell cancer. MiR-223-3p was highly expressed in clear cell renal cell cancer tissues. Clear cell renal cell cancer patients with higher miR-223-3p expression had higher tumor stages and grades and poorer prognoses. In renal cancer cells, overexpression of miR-223-3p enhanced cell proliferation and metastasis, while inhibition of miR-223-3p reduced the malignant capacity of the cells. MiR-223-3p was found to bind directly to solute carrier family 4, member 4 (SLC4A4) mRNA, thereby reducing SLC4A4 mRNA and protein expression. SLC4A4 overexpression restrained cell proliferation and metastasis by suppressing Kirsten rat sarcoma viral oncogene (KRAS) expression in renal cancer cells. SLC4A4 expression correlated negatively with miR-223-3p expression in patient samples. Given that miR-223-3p suppressed the SLC4A4/KRAS axis, miR-223-3p gene therapy could be an effective treatment for renal cancer.
引用
收藏
页码:615 / 633
页数:19
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