DNA methyltransferase 1/miR-342-3p/Forkhead box M1 signaling axis promotes self-renewal in cervical cancer stem-like cells <i>in vitro</i> and nude mice models

Our findings suggested that a novel DNMT1/miR-342-3p/FoxM1 signal axis promotes CCSLC self-renewal and presented a potential target for the treatment of CC through suppression of CCSLC self-renewal. However, this pathway has been previously implicated in CC, as evidenced by prior studies showing miR-342-3p-mediated downregulation of FoxM1 in cervical cancer cells. Additionally, research on liver cancer further supports the involvement of miR-342-3p in suppressing FoxM1 expression. While our study contributed to this body of knowledge, we did not present a completely novel axis but reinforced the therapeutic potential of targeting the DNMT1/miR-342-3p/FoxM1 axis to suppress CCSLC self-renewal in CC treatment.

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Publication Details

Journal
World Journal of Stem Cells
Published
2025-03-19
DOI
https://doi.org/10.4252/wjsc.v17.i3.99472
Citations
1
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.81
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article

DNA methyltransferase 1/miR-342-3p/Forkhead box M1 signaling axis promotes self-renewal in cervical cancer stem-like cells in vitro and nude mice models

Shaoqiang Lin, Yingxia Ning, Yebei Qiu, Xiaozheng Cao et al.
1 citations
World Journal of Stem Cells
Epigenetics and DNA Methylation
0.81
article

DNA methyltransferase 1/miR-342-3p/Forkhead box M1 signaling axis promotes self-renewal in cervical cancer stem-like cells in vitro and nude mice models

Shaoqiang Lin, Yingxia Ning, Yebei Qiu, Xiaozheng Cao, J X Lin, Huili Tang, Yuwei Song, Xiaoyu Wang, Lei Yuan, Jingyuan Li, Yaofeng Zhang, Yong Xu
article en
1 citations

Abstract

Our findings suggested that a novel DNMT1/miR-342-3p/FoxM1 signal axis promotes CCSLC self-renewal and presented a potential target for the treatment of CC through suppression of CCSLC self-renewal. However, this pathway has been previously implicated in CC, as evidenced by prior studies showing miR-342-3p-mediated downregulation of FoxM1 in cervical cancer cells. Additionally, research on liver cancer further supports the involvement of miR-342-3p in suppressing FoxM1 expression. While our study contributed to this body of knowledge, we did not present a completely novel axis but reinforced the therapeutic potential of targeting the DNMT1/miR-342-3p/FoxM1 axis to suppress CCSLC self-renewal in CC treatment.

World Journal of Stem CellsVol. 17(3)
First Affiliated Hospital of Jinan University (CN)
Good health and well-being
Openalex Percentile: Top 30%
Epigenetics and DNA Methylation
0.81
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