CircABCA13 acts as a miR‐4429 sponge to facilitate esophageal squamous cell carcinoma development by stabilizing SRXN1

Author:

Luo Junwen1,Tian Zhongxian12,Zhou Yongjia1,Xiao Zhaohua1,Park Sun Young3,Sun Hong3,Zhuang Ting4ORCID,Wang Yongjie5ORCID,Li Peiwei6,Zhao Xiaogang12ORCID

Affiliation:

1. Department of Thoracic Surgery The Second Hospital of Shandong University Jinan China

2. Key Laboratory of Chest Cancer Shandong University, The Second Hospital of Shandong University Jinan China

3. Department of Environmental Medicine New York University Grossman School of Medicine New York USA

4. Xinxiang Key Laboratory of Tumor Migration and Invasion Precision Medicine, School of Laboratory Medicine Xinxiang Medical University Xinxiang China

5. Department of Thoracic Surgery The Affiliated Hospital of Qingdao University Qingdao China

6. Institute of Medical Sciences The Second Hospital of Shandong University Jinan China

Abstract

AbstractCircular RNAs (circRNAs) play a pivotal role in the tumorigenesis and progression of various cancers. However, the role and mechanisms of circABCA13 in esophageal squamous cell carcinoma (ESCC) are largely unknown. Here, we reported that circABCA13, a novel circular RNA generated by back‐splicing of the intron of the ABCA13 gene, is highly expressed in ESCC tumor tissues and cell lines. Upregulation of circABCA13 correlated with TNM stage and a poor prognosis in ESCC patients. While knockdown of circABCA13 in ESCC cells significantly reduced cell proliferation, migration, invasion, and anchorage‐independent growth, overexpression of circABCA13 facilitated tumor growth both in vitro and in vivo. In addition, circABCA13 directly binds to miR‐4429 and sequesters miR‐4429 from its endogenous target, SRXN1 mRNA, which subsequently upregulates SRXN1 and promotes ESCC progression. Consistently, overexpression of miR‐4429 or knockdown of SRXN1 abolished malignant behavior promotion of ESCC results from circABCA13 overexpression in vitro and in vivo. Collectively, our study uncovered the oncogenic role of circABCA13 and its mechanism in ESCC, suggesting that circABCA13 could be a potential therapeutic target and a predictive biomarker for ESCC patients.

Publisher

Wiley

Subject

Cancer Research,Oncology,General Medicine

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