Transcription factor KLF4 regulates microRNA-544 that targets YWHAZ in cervical cancer
Langyong Mao1, Yan Zhang2, Xiaolong Deng1
1State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University Shanghai, China.
Abstract:
The deregulation of microRNAs has been demonstrated in various tumor processes. Here, we report that microRNA-544 (miR-544) is decreased in cervical cancer tissues compared with normal cervical tissues. To identify the mechanisms involved in miR-544 deregulation, we studied the regulation of miR-544 expression at the transcriptional level. We first identified the transcriptional start site of miR-544 by 5' rapid amplification of cDNA ends and subsequently determined the miR-544 promoter. We discovered that the transcription factor Krueppel-like factor 4 (KLF4) is involved in the transcriptional regulation of miR-544 through interaction with the miR-544 promoter. In addition, we found that miR-544 directly targets the YWHAZ oncogene and functions as a tumor suppressor in cervical cancer cells. miR-544 is involved in cell cycle regulation and suppresses cervical cancer cell proliferation, colony formation, migration and invasion in a manner associated with YWHAZ downregulation. In summary, our findings demonstrate that KLF4 upregulates miR-544 transcription by activating the miR-544 promoter and that miR-544 functions as a tumor suppressor by targeting YWHAZ. Therefore, miR-544 may be a potential novel therapeutic target and prognostic marker for cervical cancer.
Insights
MicroRNA-544 (miR-544) is downregulated in cervical cancer. Krueppel-like factor 4 (KLF4) activates miR-544 transcription, which suppresses tumor growth by targeting the YWHAZ oncogene.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA deregulation is implicated in various cancers.
- MicroRNA-544 (miR-544) shows decreased expression in cervical cancer tissues.
Purpose of the Study:
- To investigate the mechanisms behind miR-544 deregulation in cervical cancer.
- To identify the role of miR-544 as a tumor suppressor in cervical cancer.
Main Methods:
- 5' rapid amplification of cDNA ends (5' RACE) to identify the transcriptional start site.
- Promoter analysis to determine regulatory elements.
- Target gene identification and functional assays.
Main Results:
- KLF4 directly binds to the miR-544 promoter, upregulating its transcription.
- miR-544 directly targets and downregulates the YWHAZ oncogene.
- miR-544 inhibits cervical cancer cell proliferation, migration, and invasion.
Conclusions:
- KLF4-mediated upregulation of miR-544 acts as a tumor suppressor in cervical cancer.
- miR-544 targets YWHAZ, impacting cell cycle regulation.
- miR-544 presents potential as a therapeutic target and prognostic marker for cervical cancer.
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