Oncotarget

Research Papers:

miR-455-5p promotes cell growth and invasion by targeting SOCO3 in non-small cell lung cancer

Junfeng Wang, Yanbo Wang, Dawei Sun, Jianlong Bu, Fenghai Ren, Benkun Liu, Shibo Zhang, Zigeng Xu, Sainan Pang and Shidong Xu _

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Oncotarget. 2017; 8:114956-114965. https://doi.org/10.18632/oncotarget.22565

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Abstract

Junfeng Wang1, Yanbo Wang1, Dawei Sun1, Jianlong Bu1, Fenghai Ren1, Benkun Liu1, Shibo Zhang1, Zigeng Xu1, Sainan Pang1 and Shidong Xu1

1The Department of Thoracic Surgery, Harbin Medical University Cancer Hospital, Harbin 150081, China

Correspondence to:

Shidong Xu, email: xusd163@163.com

Keywords: miR-455-5p; SOCO3; invasion; non-small cell lung cancers

Received: January 23, 2017    Accepted: August 29, 2017    Published: November 20, 2017

ABSTRACT

Non-small cell lung cancer (NSCLC) is the most common type of lung cancer. miR-455-5p has increased expression and the ability to promote tumorigenesis in certain cancers. However, the role of miR-455-5p in NSCLC has not been sufficiently investigated. SOCS3 (suppressor of cytokine signaling 3), an important tumor suppressor, is often aberrantly inactivated in various tumors, but it is currently unclear whether SOCO3 is a target of miR-455-5p. In the present study, we investigated the role of miR-455-5p in NSCLC. We found that the expression of miR-455-5p was up-regulated in NSCLC tumor tissues compared to corresponding noncancerous tissues, and its expression was correlated with metastasis and tumor node metastasis in NSCLC tissue. We then showed that miR-455-5p promoted migration, invasion and proliferation in NSCLC cell lines. Additionally, we also found that SOCS3 was the direct target gene of miR-455-5p. Consistently, the expression of SOCS3 was negatively correlated with the expression of miR-455-5p in NSCLC tissues. We further show that aberrant miR-455-5p expression is partially controlled by activated ERK signaling in NSCLC. Therefore, miR-455-5p could enhance the growth and metastasis of NSCLC by inhibiting SOCS3, thus providing a potential molecular therapeutic target for the treatment of NSCLC patients.


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