Effects of HMGB-1 overexpression on cell-cycle progression in MCF-7 cells

J Korean Med Sci. 2004 Jun;19(3):321-6. doi: 10.3346/jkms.2004.19.3.321.

Abstract

High mobility group-1 (HMGB-1) enhances the DNA interactions and possesses a transcriptional activation potential for several families of sequence-specific transcriptional activators. In order to examine the effect of HMGB-1 on the cell cycle progression in MCF-7 cells, the HMGB-1 expression vector was transfected into synchronized MCF-7 cells, and the effect of HMGB-1 overexpression on the cell cycle was examined. The HMGB-1 protein level in the transfected cells increased 4.87-fold compared to the non-transfected cells. There were few changes in the cell cycle phase distribution after HMGB-1 overexpression in the MCF-7 cells. Following the estrogen treatment, the cell cycle progressed in both the HMGB-1 overexpressed MCF-7 and the mock-treated cells. However, a larger proportion of HMGB-1 overexpressing MCF-7 cells progressed to the either S or G2 phase than the mock-treated cells. The mRNA levels of the cell cycle regulators changed after being treated with estrogen in both the HMGB-1 overexpressing MCF-7 and the mock-treated cells, but the changes in the expression level of the cell cycle regulator genes were more prominent in the HMGB-1 overexpressing MCF-7 cells than in the mock-treated cells. In conclusion, HMGB-1 overexpression itself does not alter the MCF-7 cell cycle progression, but the addition of estrogen to the HMGB-1 overexpressing MCF-7 cells appears to accelerate the cell cycle progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cell Cycle
  • Cell Line, Tumor
  • Densitometry
  • Estrogens / metabolism
  • G2 Phase
  • Genetic Vectors
  • HMGB1 Protein / biosynthesis*
  • Humans
  • Kinetics
  • Oligonucleotides / chemistry
  • Plasmids / metabolism
  • Protein Structure, Tertiary
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • S Phase
  • Time Factors
  • Transcriptional Activation
  • Transfection

Substances

  • Estrogens
  • HMGB1 Protein
  • Oligonucleotides
  • RNA, Messenger