LncRNA HOTAIR promotes the migration and invasion of cervical cancer through DNMT3B/LATS1/ YAP1 pS127 axis

• DOI: 10.1016/j.repbio.2024.100893
• Publication Date: 2024-05-15T21:18:39Z
• Authors: Zhihao Zhang; Xianyi Zhou; Jiulin Li; Qinghui Meng; Peng Zheng
• Keywords: DNA Methyltransferase 3B; Mice, Inbred BALB C; Uterine Cervical Neoplasms; Mice, Nude; YAP-Signaling Proteins; Protein Serine-Threonine Kinases; DNA Methylation; Gene Expression Regulation, Neoplastic; Mice; Cell Movement; Cell Line, Tumor; Humans; Animals; RNA, Long Noncoding; Female; Neoplasm Invasiveness; DNA (Cytosine-5-)-Methyltransferases; Phosphorylation; Transcription Factors; Adaptor Proteins, Signal Transducing

Metastasis is the hallmark of cancer that is responsible for the greatest number of cancer-related deaths. As a critical regulator of the Hippo pathway, the phosphorylation status of Yes-associated protein 1 (YAP1), mainly at S127, is critical for its oncogenic function. Herein, we aim to investigate the precise molecular mechanism between long noncoding RNA HOX transcript antisense RNA (HOTAIR) and YAP1 phosphorylation in regulating tumor migration and invasion. In this study, we showed that inhibition of HOTAIR significantly decreased the migration and invasion of cancer cells both in vitro and in vivo through elevating the phosphorylation level of YAP1 on serine 127, demonstrating a tumor suppressive role of YAP1 S127 phosphorylation. Through bisulfite sequencing PCR (BSP), we found that inhibition of HOTAIR dramatically increased Large Tumor Suppressor Kinase 1 (LATS1) expression by regulating LATS1 methylation via DNA methyltransferase 3β (DNMT3B). In accordance with this observation, DNMT3B just only altered the distribution of YAP1 in the cytoplasm and the nucleus by inhibiting its phosphorylation, but did not change its total expression. Mechanistically, we discovered that HOTAIR suppressed YAP1 S127 phosphorylation by regulating the methylation of LATS1 via DNMT3B, the consequence of which is the translocation of YAP1 into the nucleus, reinforcing its coactivating transcriptional function, which in turn promotes the migration and invasion of cancer cells. Collectively, our data reveal that the phosphorylation of YAP1 S127 plays a vital role in the function of HOTAIR in tumorigenicity, and should be taken into consideration in future therapeutic strategies for cervical cancer.