Roles of microRNAs and Long Non-Coding RNAs Encoded by Parasitic Helminths in Human Carcinogenesis

Int J Mol Sci. 2022 Jul 25;23(15):8173. doi: 10.3390/ijms23158173.

Abstract

Infectious agents such as viruses, bacteria, and parasites can lead to cancer development. Infection with the helminthic parasite Schistosoma haematobium can cause cancer of the urinary bladder in humans, and infection with the parasites Clonorchis sinensis and Opisthorchis viverrini can promote cholangiocarcinoma. These three pathogens have been categorized as "group 1: carcinogenic to humans" by the International Agency for Research on Cancer (IARC). Additionally, the parasite Schistosoma japonicum has been associated with liver and colorectal cancer and classified as "group 2B: possibly carcinogenic to humans". These parasites express regulatory non-coding RNAs as microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), which modulate genic expression in different biological processes. In this review, we discuss the potential roles of miRNAS and lncRNAs encoded by helminthic parasites that are classified by the IARC as carcinogenic and possibly carcinogenic to humans. The miRNAs of these parasites may be involved in carcinogenesis by modulating the biological functions of the pathogen and the host and by altering microenvironments prone to tumor growth. miRNAs were identified in different host fluids. Additionally, some miRNAs showed direct antitumoral effects. Together, these miRNAs show potential for use in future therapeutic and diagnostic applications. LncRNAs have been less studied in these parasites, and their biological effects in the parasite-host interaction are largely unknown.

Keywords: cancer; carcinogenic parasite; fibrosis; helminths; infections; inflammation; long non-coding RNA; microRNA; polarization of immune cells.

Publication types

  • Review

MeSH terms

  • Animals
  • Bile Duct Neoplasms*
  • Bile Ducts, Intrahepatic
  • Carcinogenesis / genetics
  • Cholangiocarcinoma*
  • Helminths* / genetics
  • Humans
  • MicroRNAs* / genetics
  • RNA, Long Noncoding* / genetics
  • Tumor Microenvironment

Substances

  • MicroRNAs
  • RNA, Long Noncoding

Grants and funding

This research received no external funding.