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A DLEU2/E2F1 regulatory axis promotes migration and invasion phenotypes in cervical squamous cell carcinoma
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  • Published: 06 May 2026

A DLEU2/E2F1 regulatory axis promotes migration and invasion phenotypes in cervical squamous cell carcinoma

  • Min He1,
  • Shiyi Huang3,
  • Mingjiang Wang3,
  • Tangrui Zhu4,
  • Jinhua Ding1,
  • Yitao Wang3,
  • Mingbo Liu5,6 &
  • …
  • Hanlu Wen2 

Scientific Reports , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Cancer
  • Cell biology
  • Molecular biology
  • Oncology

Abstract

Cervical squamous cell carcinoma (CSCC), the most prevalent form of cervical cancer, is often diagnosed at advanced stages with limited treatment efficacy. Cell migration and invasion are critical steps, yet its molecular mechanisms remain poorly understood. This study investigates the role of the long non‑coding RNA DLEU2 in CSCC migration and invasion. RNA sequencing of 7 invasive CSCC and 7 normal cervical tissues revealed significant upregulation of DLEU2 in tumors, which correlated with poor prognosis in advanced‑stage patients. Functionally, DLEU2 knockdown suppressed, while its overexpression promoted, cancer cell migration and invasion in vitro. Mechanistically, we identified a DLEU2/E2F1 regulatory axis: E2F1 transcriptionally activates DLEU2, and DLEU2 in turn interacts with and may regulate E2F1 at transcription and post‑transcriptional level. Ectopic overexpression of E2F1 rescued the migratory and invasive impairments induced by DLEU2 silencing. Furthermore, DLEU2 regulated key migration and invasion‑related genes, including SNAI2 and MMP9. Together, our findings suggest an association between DLEU2 and E2F1 that may contribute to pro-migratory and pro-invasive phenotypes in CSCC, potentially offering this axis as a candidate therapeutic target.

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Funding

This study was sponsored by Natural Science Foundation of Chongqing, China (Grant number: CSTB2022NSCQ-MSX0062 and CSTB2022NSCQ-MSX0264) and Chongqing Jiulongpo District Science and Technology Plan Project (Science and Health Joint) (2024-04-030-Y).

Author information

Authors and Affiliations

  1. Department of Obstetrics and Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China

    Min He & Jinhua Ding

  2. Jiulongpo District Center for Disease Control and Prevention, Chongqing, China

    Hanlu Wen

  3. Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, China

    Shiyi Huang, Mingjiang Wang & Yitao Wang

  4. West China School of Pharmacy, Sichuan University, Chengdu, 610041, China

    Tangrui Zhu

  5. Department of Obstetrics and Gynecology, Women and Children’s Hospital of Chongqing Medical University, Chongqing, China

    Mingbo Liu

  6. Department of Obstetrics and Gynecology, Chongqing Health Center for Women and Children, Chongqing, China

    Mingbo Liu

Authors
  1. Min He
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  2. Shiyi Huang
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  3. Mingjiang Wang
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  4. Tangrui Zhu
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  5. Jinhua Ding
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  6. Yitao Wang
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  7. Mingbo Liu
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  8. Hanlu Wen
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Corresponding authors

Correspondence to Mingbo Liu or Hanlu Wen.

Ethics declarations

Ethics statement

This study was approved by the Ethics Committee of the First Affiliated Hospital of Chongqing Medical University (Approval No. 2023-78) and conducted in accordance with the Declaration of Helsinki (1964) and its later amendments, as well as relevant institutional and international ethical guidelines. No animal experiments were performed. Written informed consent was obtained from all participants or their legal guardians prior to inclusion in the study, including for the use of human tissue samples.

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The authors declare no competing interests.

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Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

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Cite this article

He, M., Huang, S., Wang, M. et al. A DLEU2/E2F1 regulatory axis promotes migration and invasion phenotypes in cervical squamous cell carcinoma. Sci Rep (2026). https://doi.org/10.1038/s41598-026-51939-4

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  • Received: 04 February 2026

  • Accepted: 30 April 2026

  • Published: 06 May 2026

  • DOI: https://doi.org/10.1038/s41598-026-51939-4

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Keywords

  • lncRNA DLEU2
  • Cervical cancer
  • Migration
  • Invasion
  • E2F1
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