Nuclear-localized CTEN is a novel transcriptional regulator and promotes cancer cell migration through its downstream target CDC27

• Published in: Journal of physiology and biochemistry Vol. 79; no. 1; pp. 163 - 174
• Main Authors: Wang, Yi-Xuan, Huang, Chun-Yang, Chiu, Hsiao-Ju, Huang, Po-Han, Chien, Hung-Ting, Jwo, Si-Han, Liao, Yi-Chun
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.02.2023; Springer; Springer Nature B.V
• Subjects: Accumulation; Animal Physiology; Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome; Biomedical and Life Sciences; Biomedicine; Cancer; Cell adhesion; Cell adhesion & migration; Cell Adhesion - physiology; Cell division; Cell migration; Cell Movement; Chromatin; Colorectal cancer; Colorectal carcinoma; Cycle protein; Deoxyribonucleic acid; DNA; Ethylenediaminetetraacetic acid; Gene expression; Genes; Genetic aspects; Genetic transcription; Human Physiology; Humans; Localization; Metastasis; Microfilament Proteins - genetics; Neoplasms; Original Article; Proteins; RNA; RNA, Messenger - genetics; Tensin; Tensins - genetics; Tensins - metabolism; Transcription; Transcription initiation; Nuclear-localized; Transcriptional regulator; CTEN; Cell migration; CDC27
• ISSN: 1138-7548; 1877-8755
• DOI: 10.1007/s13105-022-00932-2

C-terminal tensin-like (CTEN) is a tensin family protein typically localized to the cytoplasmic side of focal adhesions, and primarily contributes to cell adhesion and migration. Elevated expression and nuclear accumulation of CTEN have been reported in several types of cancers and found to be associated with malignant behaviors. However, the function of nuclear CTEN remains elusive. In this study, we report for the first time that nuclear CTEN associates with chromatin DNA and occupies the region proximal to the transcription start site in several genes. The mRNA expression level of CTEN positively correlates with that of one of its putative target genes, cell division cycle protein 27 (CDC27), in a clinical colorectal cancer dataset, suggesting that CTEN may play a role in the regulation of CDC27 gene expression. Furthermore, we demonstrated that CTEN is recruited to the promoter region of the CDC27 gene and that the mRNA expression and promoter activity of CDC27 are both reduced when CTEN is downregulated. In addition, we found that enhanced nuclear accumulation of CTEN in HCT116 cells by overexpression of CTEN fused with nuclear localization signals increases CDC27 transcript levels and promoter activity. The increased nuclear-localized CTEN also significantly promotes cell migration, and the migratory ability is suppressed when CDC27 is knocked down. These results demonstrate that nuclear CTEN regulates CDC27 expression transcriptionally and promotes cell migration through CDC27. Our findings provide new insights into CTEN moonlighting in the nucleus as a DNA-associated protein and transcriptional regulator involved in modulating cancer cell migration.