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微小RNA-338-3p在肾细胞癌中的肿瘤抑制作用。

The tumor suppressor role of microRNA-338-3p in renal cell carcinoma.

作者信息

Huang Yidong, Wu Yang, Zeng Li, Shan Wei, Huang Lugang

机构信息

Department of Pediatric Surgery, West China Hospital of Sichuan University, Chengdu, Sichuan 610041, P.R. China.

出版信息

Oncol Lett. 2018 Aug;16(2):2195-2200. doi: 10.3892/ol.2018.8914. Epub 2018 Jun 6.

DOI:10.3892/ol.2018.8914
PMID:30008918
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6036501/
Abstract

Human renal cell carcinoma (RCC) is the most common type of kidney malignancy in adults accounting for 2-3% of all adult malignancies. In China, RCC accounts for ~0.5% of all cancer-associated mortalities, ranking 16th among all cancer types. For early-stage RCC, surgery is the recommended treatment. Molecularly targeted therapy is the preferred first-line treatment for clear-cell RCC. However, more potential targets are required. MicroRNA-338-3p (miR-338-3p) functions as a tumor suppressor in various cancers, but has not been studied in RCC. Accordingly, the present study investigated the role of miR-338-3p of RCC. It was demonstrated that miR-338-3p was present at low levels in RCC tissues. Also, overexpression of miR-338-3p inhibited cell proliferation and promoted cell apoptosis, and downregulation of miR-338-3p promoted cell proliferation. The 3' untranslated region of AKT serine/threonine kinase 3 was targeted by miR-338-3p. In conclusion, the data of the present study revealed the inhibitory function of miR-338-3p in RCC and suggested that miR-338-3p is novel therapeutic target for RCC, but further investigation is needed.

摘要

人类肾细胞癌(RCC)是成人中最常见的肾脏恶性肿瘤类型,占所有成人恶性肿瘤的2%-3%。在中国,RCC占所有癌症相关死亡人数的约0.5%,在所有癌症类型中排名第16位。对于早期RCC,推荐的治疗方法是手术。分子靶向治疗是透明细胞RCC的首选一线治疗方法。然而,还需要更多潜在的靶点。微小RNA-338-3p(miR-338-3p)在多种癌症中发挥肿瘤抑制作用,但尚未在RCC中进行研究。因此,本研究调查了miR-338-3p在RCC中的作用。结果表明,miR-338-3p在RCC组织中的表达水平较低。此外,miR-338-3p的过表达抑制细胞增殖并促进细胞凋亡,而miR-338-3p的下调则促进细胞增殖。miR-338-3p靶向AKT丝氨酸/苏氨酸激酶3的3'非翻译区。总之,本研究的数据揭示了miR-338-3p在RCC中的抑制作用,并表明miR-338-3p是RCC的新型治疗靶点,但还需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/6036501/8b8cd6a4968b/ol-16-02-2195-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/6036501/9652761f9ec2/ol-16-02-2195-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/6036501/3a6bf1d2035e/ol-16-02-2195-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/6036501/006ea00d80fe/ol-16-02-2195-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/6036501/8b8cd6a4968b/ol-16-02-2195-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/6036501/9652761f9ec2/ol-16-02-2195-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/6036501/3a6bf1d2035e/ol-16-02-2195-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/6036501/006ea00d80fe/ol-16-02-2195-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd0/6036501/8b8cd6a4968b/ol-16-02-2195-g04.jpg

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MicroRNA-338-3p suppresses cell proliferation and induces apoptosis of non-small-cell lung cancer by targeting sphingosine kinase 2.微小RNA-338-3p通过靶向鞘氨醇激酶2抑制非小细胞肺癌细胞增殖并诱导其凋亡。
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