Cancer stem cells: The important role of CD markers, Signaling pathways, and MicroRNAs

Pathol Res Pract. 2024 Apr:256:155227. doi: 10.1016/j.prp.2024.155227. Epub 2024 Feb 28.

Abstract

For the first time, a subset of small cancer cells identified in acute myeloid leukemia has been termed Cancer Stem Cells (CSCs). These cells are notorious for their robust proliferation, self-renewal abilities, significant tumor-forming potential, spread, and resistance to treatments. CSCs are a global concern, as it found in numerous types of cancer, posing a real-world challenge today. Our review encompasses research on key CSC markers, signaling pathways, and MicroRNA in three types of cancer: breast, colon, and liver. These factors play a critical role in either promoting or inhibiting cancer cell growth. The reviewed studies have shown that as cells undergo malignant transformation, there can be an increase or decrease in the expression of different Cluster of Differentiation (CD) markers on their surface. Furthermore, alterations in essential signaling pathways, such as Wnt and Notch1, may impact CSC proliferation, survival, and movement, while also providing potential targets for cancer therapies. Additionally, some research has focused on MicroRNAs due to their dual role as potential therapeutic biomarkers and their ability to enhance CSCs' response to anti-cancer drugs. MicroRNAs also regulate a wide array of cellular processes, including the self-renewal and pluripotency of CSCs, and influence gene transcription. Thus, these studies indicate that MicroRNAs play a significant role in the malignancy of various tumors. Although the gathered information suggests that specific CSC markers, signaling pathways, and MicroRNAs are influential in determining the destiny of cancer cells and could be advantageous for therapeutic strategies, their precise roles and impacts remain incompletely defined, necessitating further investigation.

Keywords: CD markers; Cancer Stem Cell; MicroRNAs; Signaling.

Publication types

  • Review

MeSH terms

  • Antigens, Differentiation / metabolism
  • Antineoplastic Agents* / therapeutic use
  • Humans
  • MicroRNAs* / metabolism
  • Neoplasms* / metabolism
  • Neoplastic Stem Cells / pathology
  • Signal Transduction

Substances

  • MicroRNAs
  • Antineoplastic Agents
  • Antigens, Differentiation