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Upregulated circular RNA circ_0007534 indicates an unfavorable prognosis in pancreatic ductal adenocarcinoma and regulates cell proliferation, apoptosis, and invasion by sponging miR‐625 and miR‐892b
Author(s) -
Hao Liguo,
Rong Wei,
Bai Lianjie,
Cui Hongsheng,
Zhang Shuli,
Li Yuanchun,
Chen Datong,
Meng Xin
Publication year - 2019
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.27658
Subject(s) - cancer research , apoptosis , cell growth , microrna , downregulation and upregulation , biology , cell , chemistry , gene , biochemistry , genetics
Abstract Circular RNAs (circRNAs) have been regarded as critical regulators of human diseases and biological markers in some types of malignancies, including pancreatic ductal adenocarcinoma (PDAC). Recently, circ_0007534 has been identified as a novel cancer‐related circRNA. Nevertheless, its clinical relevance, functional roles, and mechanism have not been studied in PDAC. In the current study, real‐time quantitative polymerase chain reaction (RT‐qPCR) was used to detect the expression of circ_0007534 in 60‐paired PDAC tissue samples and different cell lines. Loss‐of‐function and gain‐of‐function assays were performed to detect cell proliferation, apoptosis, and metastatic properties affected by circ_0007534. An animal study was also carried out. The luciferase reporter assay was performed to uncover the underlying mechanism of circ_0007534. As a result, circ_0007534 was overexpressed not only in PDAC tissues but also in a panel of PDAC cell lines, and this overexpression is closely associated with advanced tumor stage and positive lymph node invasion. In addition, circ_0007534 may be regarded as an independent prognostic factor for patients with PDAC. For the part of functional assays, circ_0007534 significantly increased cell proliferation, migratory, and invasive potential of PDAC cells. Circ_0007534 could inhibit cell apoptosis partly via a Bcl‐2/caspase‐3 pathway. The xenograft study further confirmed the cell growth promoting the role of circ_0007534. Mechanistically, miR‐625 and miR‐892b were sponged by circ_0007534. The oncogenic functions of circ_0007534 is partly dependent on its regulation of miR‐625 and miR‐892b. In conclusion, our study illuminates a novel circRNA that confers an oncogenic function in PDAC.