Dual Role of YY1 in HPV Life Cycle and Cervical Cancer Development

Int J Mol Sci. 2022 Mar 22;23(7):3453. doi: 10.3390/ijms23073453.

Abstract

Human papillomaviruses (HPVs) are considered to be key etiological agents responsible for the induction and development of cervical cancer. However, it has been suggested that HPV infection alone may not be sufficient to promote cervical carcinogenesis, and other unknown factors might be required to establish the disease. One of the suggested proteins whose deregulation has been linked with oncogenesis is transcription factor Yin Yang 1 (YY1). YY1 is a multifunctional protein that is involved not only in the regulation of gene transcription and protein modification, but can also control important cell signaling pathways, such as cell growth, development, differentiation, and apoptosis. Vital functions of YY1 also indicate that the protein could be involved in tumorigenesis. The overexpression of this protein has been observed in different tumors, and its level has been correlated with poor prognoses of many types of cancers. YY1 can also regulate the transcription of viral genes. It has been documented that YY1 can bind to the HPV long control region and regulate the expression of viral oncogenes E6 and E7; however, its role in the HPV life cycle and cervical cancer development is different. In this review, we explore the role of YY1 in regulating the expression of cellular and viral genes and subsequently investigate how these changes inadvertently contribute toward the development of cervical malignancy.

Keywords: HPV; YY1; cell signaling; cervical cancer; gene expression; oncogenes; transcription factors; tumor suppressors.

Publication types

  • Review

MeSH terms

  • Carcinogenesis / genetics
  • Carcinogenesis / metabolism
  • Cell Transformation, Neoplastic
  • Female
  • Humans
  • Oncogene Proteins, Viral / genetics
  • Papillomaviridae / genetics
  • Papillomavirus E7 Proteins / genetics
  • Papillomavirus Infections* / genetics
  • Uterine Cervical Neoplasms* / genetics
  • Uterine Cervical Neoplasms* / pathology
  • YY1 Transcription Factor* / genetics
  • YY1 Transcription Factor* / metabolism

Substances

  • Oncogene Proteins, Viral
  • Papillomavirus E7 Proteins
  • YY1 Transcription Factor
  • YY1 protein, human