[Growth of breast cancer cells is inhibited in vitro by cyclin E-siRNA]

Zhonghua Zhong Liu Za Zhi. 2009 Mar;31(3):170-3.
[Article in Chinese]

Abstract

Objective: To investigate the changes of biological characteristics of breast cancer cell line by cyclin E expression.

Methods: Human breast cancer cell line MCF-7 was transfected with cyclin E siRNA vector pEGFP/CCNE2. siRNA-induced silencing of cyclin E was determined by RT-PCR at RNA level and Western blot at protein level. The proliferation of MCF-7 cells and their sensitivity to chemotherapy was measured by CCK-8 assay. The cells were examined by FCM. The cell line was injected into nude mice and the tumor size was measured.

Results: The expression of cyclin E was inhibited in the MCF-7 cells. The relative expression level of cyclin E mRNA was 0.23 +/- 0.05, and that of cyclin E protein was 0.24 +/- 0.05. The cell growth was inhibited by 68.56% +/- 0.08%, and their sensitivity to chemotherapy was increased. Most cells were blocked at G(1) (77.38%), their tumorigenic ability in nude mice was reduced, and the size of tumor formed in mice of the experimental group was decreased than that of controls.

Conclusion: Inhibition of cyclin E expression in breast cancer cells can block their cell cycle at G(1) phase, reduce their cell growth, differentiation and proliferation, and increase their sensitivity to chemotherapy.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / pharmacology
  • Antimetabolites, Antineoplastic / pharmacology
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Breast Neoplasms* / metabolism
  • Breast Neoplasms* / pathology
  • Cell Cycle
  • Cell Line, Tumor
  • Cell Proliferation* / drug effects
  • Cyclin E / genetics
  • Cyclin E / metabolism*
  • Doxorubicin / pharmacology
  • Female
  • Fluorouracil / pharmacology
  • Genetic Vectors
  • Humans
  • Male
  • Mice
  • Mice, Inbred ICR
  • Mice, Nude
  • Neoplasm Transplantation
  • Paclitaxel / pharmacology
  • Plasmids
  • RNA Interference
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / genetics*
  • Transfection
  • Tumor Burden

Substances

  • Antibiotics, Antineoplastic
  • Antimetabolites, Antineoplastic
  • Antineoplastic Agents, Phytogenic
  • Cyclin E
  • RNA, Messenger
  • RNA, Small Interfering
  • Doxorubicin
  • Paclitaxel
  • Fluorouracil