DEAD-Box Helicase 27 Triggers Epithelial to Mesenchymal Transition by Regulating Alternative Splicing of Lipoma-Preferred Partner in Gastric Cancer Metastasis

• Published in: Frontiers in genetics Vol. 13; p. 836199
• Main Authors: Jin, Yirong, Yang, Suzhen, Gao, Xiaoliang, Chen, Di, Luo, Tingting, Su, Song, Shi, Yanting, Yang, Gang, Dong, Lei, Liang, Jie
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 04.05.2022
• Subjects: alternative splicing; DDX27; EMT; gastric cancer metastasis; Genetics; LPP; gastric cancer metastasis; DDX27; alternative splicing; EMT; LPP
• ISSN: 1664-8021; 1664-8021
• DOI: 10.3389/fgene.2022.836199

DEAD-box helicase 27 (DDX27) was previously identified as an important mediator during carcinogenesis, while its role in gastric cancer (GC) is not yet fully elucidated. Here, we aimed to investigate the mechanism and clinical significance of DDX27 in GC. Public datasets were analyzed to determine DDX27 expression profiling. The qRT-PCR, Western blot, and immunohistochemistry analyses were employed to investigate the DDX27 expression in GC cell lines and clinical samples. The role of DDX27 in GC metastasis was explored and . Mass spectrometry, RNA-seq, and alternative splicing analysis were conducted to demonstrate the DDX27-mediated molecular mechanisms in GC. We discovered that DDX27 was highly expressed in GCs, and a high level of DDX27 indicated poor prognosis. An increased DDX27 expression could promote GC metastasis, while DDX27 knockdown impaired GC aggressiveness. Mechanically, the LLP expression was significantly altered after DDX27 downregulation, and further results indicated that LPP may be regulated by DDX27 alternative splicing. In summary, our study indicated that DDX27 contributed to GC malignant progression a prometastatic DDX27/LPP/EMT regulatory axis.