[Expression and regulatory mechanism of S100A14 in breast cancer]

Zhonghua Zhong Liu Za Zhi. 2016 Apr;38(4):252-7. doi: 10.3760/cma.j.issn.0253-3766.2016.04.003.
[Article in Chinese]

Abstract

Objective: To explore the expression of S100A14 in breast cancer tissue, and the EGF and S100A14 feedback regulatory mechanism.

Methods: S100A14 mRNA level in 52 cases of of breast cancer and adjacent normal tissue was detected by quantitative real-time PCR. S100A14 protein in 21 cases of breast cancer and adjacent normal tissue was detected by Western blot. S100A14 mRNA after EGF treatment was detected by RT-PCR and real-time PCR. The levels of S100A14, p-ERK and t-ERK were detected by Western blot. Knocking down S100A14 expression was performed by siRNA technology.

Results: The levels of S100A14 mRNA and protein were significantly increased in breast cancer tissues (P<0.05 for both). The high expression of S100A14 was related with the recurrence of breast cancer patients (P= 0.038). S100A14 mRNA level was significantly up-regulated in the MDA-MB-453 cells (1.50±0.11) and MCF-7 cells (1.40±0.03) after 1 ng/mL EGF treatment, and 1.66±0.08 and 1.71±0.17 in the MDA-MB-453 cells after 10 ng/mL EGF treatment, significantly higher than that of the control group (1.00±0.09 and 1.00±0.03) (P<0.05 for both). In the TD47 cells, the S100A14 mRNA levels in the control, 1 ng/ml EGF and 10 ng/ml EGF + U0126 treatment groups were 1.00±0.04, 1.56±0.04 and 1.00±0.10, respectively (P<0.05).

Conclusions: The expression of S100A14 mRNA and protein is promoted by EGF through p-ERK signaling pathway in breast cancer cells. There may be a feedback loop between EGF and S100A14.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Breast / metabolism
  • Breast Neoplasms / metabolism*
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / metabolism*
  • Cell Line, Tumor
  • Down-Regulation
  • Epidermal Growth Factor / pharmacology*
  • Female
  • Humans
  • MAP Kinase Signaling System
  • MCF-7 Cells
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Neoplasm Recurrence, Local / metabolism
  • RNA, Messenger / metabolism*
  • RNA, Small Interfering
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction
  • Up-Regulation

Substances

  • Calcium-Binding Proteins
  • Neoplasm Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • S100A14 protein, human
  • Epidermal Growth Factor