A novel intronic circular RNA, circGNG7, inhibits head and neck squamous cell carcinoma progression by blocking the phosphorylation of heat shock protein 27 at Ser78 and Ser82. Issue 11 (9th September 2021)

• Record Type: Journal Article
• Authors: Ju, Houyu; Hu, Zhenrong; Wei, Dongliang; Huang, Jinyun; Zhang, Xinyi; Rui, Mengyu; Li, Zhi; Zhang, Xiaomeng; Hu, Jingzhou; Guo, Wei; Ren, Guoxin
• Is Part Of: Cancer communications. Volume 41:Issue 11(2021)
• Page Start: 1152
• Page End: 1172
• Publication Date: 2021-09-09
• Subjects: circGNG7 -- head and neck squamous cell carcinoma -- heat shock protein 27 (HSP27) -- intronic circular RNAs -- mitogen‐activated protein kinase (MAPK) signaling -- phosphorylation -- tumor suppressor; Cancer -- Periodicals; Neoplasms; Electronic journals; Periodical; Fulltext; Internet Resources; Periodicals; Periodicals; 616.994005
• DOI: 10.1002/cac2.12213
• Languages: English
• ISSNs: 2523-3548

Abstract

Abstract: Background: There is increasing evidence that circular RNAs (circRNAs) play a significant role in pathological processes including tumorigenesis. In contrast to exonic circRNAs, which are the most frequently reported circRNAs in cancer so far, the studies of intronic circRNAs have been greatly lagged behind. Here, we aimed to investigate the regulatory role of intronic circRNAs in head and neck squamous cell carcinoma (HNSCC). Methods: We conducted whole‐transcriptome sequencing with four pairs of primary tumor tissues and adjacent normal tissues from HNSCC patients. Then, we characterized circGNG7 expression in HNSCC tissues and cell lines and explored its association with the prognosis of HNSCC patients. We also identified interactions between circGNG7 and functional proteins, which alter downstream signaling that regulate HNSCC progression. Results: In this study, we identified a new intronic circRNA, circGNG7, and validated its functional roles in HNSCC progression. CircGNG7 was predominately localized to the cytoplasm, and its expression was downregulated in both HNSCC tissues andCAL27, CAL33, SCC4, SCC9, HN6, and HN30 cells. Low expression of circGNG7 was significantly correlated with poor prognosis in HNSCC patients. Consistent with this finding, overexpression of circGNG7 strongly inhibited tumor cell proliferation, colony formation, in vitro migration, and in vivo tumor growth. Mechanistically, the expression of circGNG7 in HNSCC cells was regulated by the transcription factor SMAD family member 4 (SMAD4). Importantly, we discovered that circGNG7 could bind to serine residues 78 and 82 of the functional heat shock protein 27 (HSP27), occupying its phosphorylation sites and hindering its phosphorylation, which reduced HSP27‐JNK/P38 mitogen‐activated protein kinase (MAPK) oncogenic signaling. Downregulation of circGNG7 expression in HNSCC increased HSP27‐JNK/P38 MAPK signaling and promoted tumor progression. Conclusions: Our results revealed that a new intronic circRNA, circGNG7, functions as a strong tumor suppressor and that circGNG7/HSP27‐JNK/P38 MAPK signaling is a novel mechanism by which HNSCC progression can be controlled. Abstract : That circGNG7, regulated by SMAD4, could bind with serine residues 78, and 82, occupy the phosphorylation site of functional protein HSP27, thus hinder the phosphorylation of HSP27, which reduces the HSP27‐JNK/P38 MAPK oncogenic signaling and inhibits HNSCC progression.