CD44/CD133-Positive Colorectal Cancer Stem Cells are Sensitive to Trifluridine Exposure

Sci Rep. 2019 Oct 16;9(1):14861. doi: 10.1038/s41598-019-50968-6.

Abstract

Cancer stem cells (CSCs) are involved in metastatic colorectal cancer recurrence, but no effective therapy targeting these cells is currently available. Because trifluridine (FTD)/tipiracil therapy is used for refractory colorectal cancer, we sought to determine whether FTD is effective against CSC-like cells. CD44+CD133+ high-expressing and other populations of human DLD-1 colon cancer cells were separately isolated through fluorescence-activated cell sorting. The sphere-forming activity of each population and the anti-sphere-forming effects of FTD and fluorouracil (5-FU) on CD44+CD133+ cells were then measured. CD44+CD133+ DLD-1 cells formed substantially more spheres than other cells. Moreover, treating CD44+CD133+ DLD-1 cells with subtoxic concentrations of FTD (1 µM) inhibited sphere formation, and this was superior to the effect of subtoxic concentrations (1 µM) of 5-FU. The associated inhibition rates for FTD and 5-FU were 58.2% and 26.1%, respectively. Further, CD44+CD133+ DLD-1 cells expressed higher levels of thymidine kinase 1, which is responsible for FTD phosphorylation, than DLD-1 cells, and FTD was incorporated into the DNA of CD44+CD133+ DLD-1 cells. Thus, our data show that FTD treatment is effective against CSC-like cells and might be applied as CSC-targeting chemotherapy for tumor subtypes with high CD44 and CD133 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AC133 Antigen / genetics
  • AC133 Antigen / metabolism
  • Antimetabolites, Antineoplastic / pharmacology*
  • Cell Line, Tumor
  • Colon / metabolism
  • Colon / pathology
  • Drug Combinations
  • Drug Synergism
  • Fluorouracil / pharmacology*
  • Gene Expression
  • Humans
  • Hyaluronan Receptors / genetics
  • Hyaluronan Receptors / metabolism
  • Inhibitory Concentration 50
  • Neoplastic Stem Cells / drug effects*
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Pyrrolidines / pharmacology*
  • Spheroids, Cellular / drug effects*
  • Spheroids, Cellular / metabolism
  • Spheroids, Cellular / pathology
  • Thymidine Kinase / genetics
  • Thymidine Kinase / metabolism
  • Thymine / pharmacology*
  • Trifluridine / pharmacology*

Substances

  • AC133 Antigen
  • Antimetabolites, Antineoplastic
  • CD44 protein, human
  • Drug Combinations
  • Hyaluronan Receptors
  • PROM1 protein, human
  • Pyrrolidines
  • Thymidine Kinase
  • thymidine kinase 1
  • tipiracil
  • Thymine
  • Trifluridine
  • Fluorouracil