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Long non‐coding RNA H19 suppresses retinoblastoma progression via counteracting miR‐17‐92 cluster
Author(s) -
Zhang Aihui,
Shang Weiwei,
Nie Qiaoli,
Li Ting,
Li Suhui
Publication year - 2018
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.26521
Subject(s) - retinoblastoma , retinoblastoma protein , cancer research , cell cycle , cell growth , cell cycle checkpoint , long non coding rna , biology , apoptosis , suppressor , chemistry , microbiology and biotechnology , rna , gene , genetics
Long non‐coding RNAs (lncRNAs) are frequently dysregulated and play important roles in many cancers. lncRNA H19 is one of the earliest discovered lncRNAs which has diverse roles in different cancers. However, the expression, roles, and action mechanisms of H19 in retinoblastoma are still largely unknown. In this study, we found that H19 is downregulated in retinoblastoma tissues and cell lines. Gain‐of‐function and loss‐of‐function assays showed that H19 inhibits retinoblastoma cell proliferation, induces retinoblastoma cell cycle arrest and cell apoptosis. Mechanistically, we identified seven miR‐17‐92 cluster binding sites on H19, and found that H19 directly bound to miR‐17‐92 cluster via these seven binding sites. Through binding to miR‐17‐92 cluster, H19 relieves the suppressing roles of miR‐17‐92 cluster on p21. Furthermore, H19 represses STAT3 activation induced by miR‐17‐92 cluster. Hence, our results revealed that H19 upregulates p21 expression, inhibits STAT3 phosphorylation, and downregulates the expression of STAT3 target genes BCL2, BCL2L1, and BIRC5. In addition, functional assays demonstrated that the mutation of miR‐17‐92 cluster binding sites on H19 abolished the proliferation inhibiting, cell cycle arrest and cell apoptosis inducing roles of H19 in retinoblastoma. In conclusion, our data suggested that H19 inhibits retinoblastoma progression via counteracting the roles of miR‐17‐92 cluster, and implied that enhancing the action of H19 may be a promising therapeutic strategy for retinoblastoma.