Abstract

Cancer stem cells (CSCs) have been reported in various hematopoietic and solid tumors, therefore, are considered to promote cancer progression, metastasis, recurrence and drug resistance. However, regulation of CSCs at the molecular level is not fully understood. microRNAs (miRNAs) have been identified as key regulators of CSCs by modulating their major functions: self-renewal capacity, invasion, migration and proliferation. Various studies suggest that metformin, an anti-diabetic drug, has an anti-tumor activity but its precise mechanism of action has not been understood. The present article was written in accordance to the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. We systematically reviewed evidence for metformin’s ability to eradicate CSCs through modulating the expression of miRNAs in various solid tumors. PubMed and MEDLINE were searched from January 1990 to January 2020 for in vitro studies. Two authors independently selected and reviewed articles according to predefined eligibility criteria and assessed risk of bias of included studies. Four papers met the inclusion criteria and presented low risk bias. All of the included studies reported a suppression of CSCs’ major function after metformin dosage. Moreover, it was showed that metformin anti-tumor mechanism of action is based on regulation of miRNAs expression. Metformin inhibited cell survival, clonogenicity, wound-healing capacity, sphere formation and promotes chemosensitivity of tumor cells. Due to the small number of publications, aforementioned evidences are limited but may be consider as background for clinical studies.

Highlights

  • Cancer stem cells (CSCs) are a subpopulation of cancer cells that have the ability to self-renew, differentiate into different cell types and to arrest in the G0 phase

  • In the 1990s, CSCs were identified in acute myeloid leukemia (AML) [3,4]

  • Reduction of SP fraction occurs as a result of miR-27b suppression of the ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) gene that leads to the inhibition of the expression and cell surface localization of ATP-binding cassette super-family G member 2 (ABCG2) transporter

Read more

Summary

Introduction

Cancer stem cells (CSCs) are a subpopulation of cancer cells that have the ability to self-renew, differentiate into different cell types and to arrest in the G0 phase. Since the first studies on CSCs’ existence, the expression of cell surface markers has been used to isolate and identify CSCs, differentiating them from many types of cancers [4,5,6]. There are plenty of common or unique surface markers that have been associated with solid or hematopoietic tumors, for example, CD34+ CD38− for AML [4]; CD44+ CD24− /lowLin- [5] and ALDH+ [10] for breast cancer; CD44+ [11], CD44+ α2β1+ [12] and ALDH+ [13] for prostate cancer; CD44+ CD117+ [7], CD24+ [14], Cells 2020, 9, 1401; doi:10.3390/cells9061401 www.mdpi.com/journal/cells

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call