4.7 Review

The Dysregulation of MicroRNAs in the Development of Cervical Pre-Cancer-An Update

Journal

Publisher

MDPI
DOI: 10.3390/ijms23137126

Keywords

cervical pre-cancer; microRNA; cervical cancer; biomarkers; CIN; SIL; HPV; DNA damage response; DDR; miR

Funding

  1. Research Talent Hub [IsP/004/22, PsH 104/21]
  2. Innovation and Technology Fund
  3. ITC STEM Internship Scheme
  4. Incu-Bio Program, Hong Kong Science and Technology Parks
  5. City University of Hong Kong, New Research Initiatives/Infrastructure Support from Central (APRC) [9610589]
  6. City University of Hong Kong New Research Initiatives/Infrastructure Support from Central (APRC) [9610589]

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This review focuses on the dysregulation of miRNAs in the pre-stage of cervical cancer. Several dysregulated miRNAs have been identified and found to be associated with the DNA damage response and cell growth response induced by human papillomavirus (HPV) infection. However, discrepancies in sample types, HPV status, expression measurement, and analysis methods have led to non-aligned results across studies. This review provides insight into identifying miRNAs involved in early pathogenic processes and highlights their potential as biomarkers for cervical pre-cancer.
Globally in 2020, an estimated -600,000 women were diagnosed with and 340,000 women died from cervical cancer. Compared to 2012, the number of cases increased by 7.5% and the number of deaths increased by 17%. MiRNAs are involved in multiple processes in the pathogenesis of cervical cancer. Dysregulation of miRNAs in the pre-stage of cervical cancer is the focus of this review. Here we summarize the dysregulated miRNAs in clinical samples from cervical pre-cancer patients and relate them to the early transformation process owing to human papillomavirus (HPV) infection in the cervical cells. When HPV infects the normal cervical cells, the DNA damage response is initiated with the involvement of HPV's El and E2 proteins. Later, cell proliferation and cell death are affected by the E6 and E7 proteins. We find that the expressions of miRNAs in cervical pre-cancerous tissue revealed by different studies seldom agreed with each other. The discrepancy in sample types, samples' HPV status, expression measurement, and methods for analysis contributed to the non-aligned results across studies. However, several miRNAs (miR-34a, miR-9, miR-21, miR-145, and miR-375) were found to be dysregulated across multiple studies. In addition, there are hints that the DNA damage response and cell growth response induced by HPV during the early transformation of the cervical cells are related to these miRNAs. Currently, no review articles analyse the relationship between the dysregulated miRNAs in cervical pre-cancerous tissue and their possible roles in the early processes involving HPV's protein encoded by the early genes and DNA damage response during normal cell transformation. Our review provides insight on spotting miRNAs involved in the early pathogenic processes and pointing out their potential as biomarker targets of cervical pre-cancer.

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