| RRC ID |
70029
|
| 著者 |
Chen X, Wang Z, Zhao X, Zhang L, Zhou L, Li X, Ge C, Zhao F, Chen T, Xie H, Cui Y, Tian H, Li H, Yao M, Li J.
|
| タイトル |
STAT5A modulates CDYL2/SLC7A6 pathway to inhibit the proliferation and invasion of hepatocellular carcinoma by targeting to mTORC1.
|
| ジャーナル |
Oncogene
|
| Abstract |
Chromodomain Y-like 2 (CDYL2), as a member of CDY family known to be involved in spermatogenesis, has been reported to participate in breast cancer development recently, but its exact biological role in hepatocellular carcinoma (HCC) remains unclear. Here, we observed that CDYL2 was down-regulated in human primary HCC tissues and the low levels of CDYL2 expression were correlated with poor survival. Gain- and loss-of-function experiments showed that CDYL2 inhibited the proliferation and metastasis of HCC cells in vitro and in vivo. Mechanistically, CDYL2 down-regulates solute carrier family 7 member 6 (SLC7A6) by decreasing the enrichment of H3K4me3 on the promoter region of SLC7A6. Additionally, we also found that signal transducer and activator of transcription 5A (STAT5A) could directly and positively regulate the expression of CDYL2. Thus, CDYL2 was regulated by STAT5A, and suppressed the amino acid transportation through down-regulation of SLC7A6, and then inhibits the mTORC1/S6K pathway, a master regulator of cell growth. Consistently, CDYL2 expression correlated significantly with STAT5A and SLC7A6 expression in HCC. Collectively, we propose a model for a STAT5A/CDYL2/SLC7A6 axis that provides novel insight into CDYL2, which may serve as a potential factor for predicting prognosis and a therapeutic target for HCC patients.
|
| 巻・号 |
41(17)
|
| ページ |
2492-2504
|
| 公開日 |
2022-4-1
|
| DOI |
10.1038/s41388-022-02273-2
|
| PII |
10.1038/s41388-022-02273-2
|
| PMID |
35314791
|
| MeSH |
Amino Acid Transport Systems, Basic* / genetics
Carcinoma, Hepatocellular* / pathology
Cell Line, Tumor
Cell Movement
Cell Proliferation / genetics
Gene Expression Regulation, Neoplastic
Humans
Liver Neoplasms* / pathology
Mechanistic Target of Rapamycin Complex 1 / genetics
Mechanistic Target of Rapamycin Complex 1 / metabolism
STAT5 Transcription Factor* / genetics
STAT5 Transcription Factor* / metabolism
Tumor Suppressor Proteins / metabolism
|
| IF |
7.971
|
| リソース情報 |
| ヒト・動物細胞 |
HuH-7(RCB1366) |
