1H-magnetic resonance spectroscopic observation of cultured malignant cells pharmacologically induced to different phenotypes

Acad Radiol. 1996 Sep;3(9):742-50. doi: 10.1016/s1076-6332(96)80414-4.

Abstract

Rationale and objectives: We evaluated the 1H nuclear magnetic resonance spectra of malignant cells after the administration of drugs that cause morphologic changes.

Methods: 1H spectra of a human lung adenocarcinoma cell line cultured with interferon gamma, dexamethasone, or sodium butyrate were obtained. The peaks were assigned by two-dimensional homonuclear Hartmann-Hahn spectroscopy spectra of the cells and their perchloric acid extracts. Differential spectra were used to evaluate relative changes in the peaks.

Results: In the control culture, choline/phosphocholine peaks were increased in the cell-growth phase, and the 1.26-ppm peak was increased in the confluent state. Treatment by interferon gamma and dexamethasone induced reproducible changes in the peaks of differential spectra corresponding to 1.26 ppm, choline/phosphocholine, and glutamate/glutamine. Dexamethasone treatment broadened lipid peaks. Changes after treatment with sodium butyrate were obscure. Microscopically, cells were induced to morphologically different phenotypes by each drug.

Conclusion: Cells induced to exhibit morphologically different phenotypes present different 1H spectra.

MeSH terms

  • Adenocarcinoma / metabolism*
  • Adenocarcinoma / physiopathology
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents, Hormonal / pharmacology*
  • Butyrates / pharmacology*
  • Butyric Acid
  • Choline / analysis
  • Choline / metabolism
  • Creatine / analysis
  • Creatine / metabolism
  • Dexamethasone / pharmacology*
  • Glutamic Acid / analysis
  • Glutamic Acid / metabolism
  • Glutamine / analysis
  • Glutamine / metabolism
  • Histone Deacetylase Inhibitors*
  • Humans
  • Hydrogen
  • Interferon-gamma / pharmacology*
  • Lactates / analysis
  • Lactates / metabolism
  • Lung Neoplasms / metabolism*
  • Lung Neoplasms / physiopathology
  • Magnetic Resonance Spectroscopy*
  • Phenotype
  • Phospholipids / analysis
  • Phospholipids / metabolism
  • Phosphorylcholine / analysis
  • Phosphorylcholine / metabolism
  • Triglycerides / analysis
  • Triglycerides / metabolism
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • Antineoplastic Agents, Hormonal
  • Butyrates
  • Histone Deacetylase Inhibitors
  • Lactates
  • Phospholipids
  • Triglycerides
  • Glutamine
  • Phosphorylcholine
  • Butyric Acid
  • Glutamic Acid
  • Dexamethasone
  • Hydrogen
  • Interferon-gamma
  • Creatine
  • Choline