Role of Sulfation Pharmacogenetics in Breast Cancer Treatment with 2-Methoxyestradiol

Abstract

2-ME2 is an endogenous estrogen metabolite that inhibits the proliferation of breast and other human cancer cell lines. 2-ME2 also has potent anti-angiogenic and anti-tubulin properties, and it may inhibit estrogen- induced carcinogenesis in the mammary gland. We set out to test the hypothesis that 2-ME2 might be a substrate for sulfate conjugation and, therefore, that individual variations in the sulfation of 2-ME2 might contribute to individual differences in its metabolism, pharmacokinetics and therapeutic efficacy. As a first step, we tested 2-ME2 as a substrate for 7 human sulfotransferase (SULT) isoforms -- as well as all of the common allozymes for SULT 1 Al and 1A2.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2001
Accession Number
ADB275851

Entities

People

  • Araba A. Adjei

Tags

DTIC Thesaurus Topics

  • Biomedical Research
  • Breast Cancer
  • Cell Line
  • Cells
  • Computer Programs
  • Computers
  • Contractors
  • Enzyme Kinetics
  • Estrogens
  • Genetics
  • Government Procurement
  • Governments
  • Mammary Glands
  • Maryland
  • Metabolism
  • Neoplasms
  • Pharmacogenetics

Fields of Study

  • Biology
  • Chemistry

Readers

  • Breast cancer cell signaling and growth regulation.
  • Molecular and genetic basis of cancer.
  • Oncology (Cancer Research).