[Metallothionein and its isoform genes expression in the human pancreatic cancer cell strains and their function]

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005 Oct;27(5):619-23.
[Article in Chinese]

Abstract

Objective: To compare the expression of metallothionein (MT) genes and proteins in six human pancreatic cancer cell strains and two human pancreatic cancer drug-resistant cell strains and to explore the relationship between the expression of the MT and pancreatic cancer cell chemo-resistance.

Methods: Reverse transcriptase-polymerase chain reaction (RT-PCR) was used to determine the MT isoform-specific mRNA, and cadmium/hemoglobin saturation-electrochemistry to determine MT protein levels.

Results: MT protein expression in the pancreatic cancer cell strains was encoded by MT-1A, MT-1B, MT-1E, MT-1F, MT-1G, MT-1X, and MT-2A genes. The expression of MT proteins was upregulated and MT-1B, MT-1E, MT-1X, MT-2A genes overexpressed in human pancreatic cancer drug-resistant cell lines (P < 0.05).

Conclusion: Expressions of MT proteins and genes correlate with the proliferation and chemoresistance of human pancreatic cancer cell strains.

Publication types

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

MeSH terms

  • Cell Division / genetics
  • Drug Resistance, Neoplasm / genetics
  • Humans
  • Metallothionein / biosynthesis
  • Metallothionein / genetics
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology
  • RNA, Messenger / genetics
  • Tumor Cells, Cultured

Substances

  • RNA, Messenger
  • Metallothionein