Targeting Gallium to Cancer Cells through the Folate Receptor

Authors

  • Nerissa Viola-Villegas Department of Chemistry, Syracuse University, Syracuse, NY 13244-4100, U.S.A.
  • Anthony Vortherms Department of Chemistry, Syracuse University, Syracuse, NY 13244-4100, U.S.A.
  • Robert P. Doyle Department of Chemistry, Syracuse University, Syracuse, NY 13244-4100, U.S.A.

DOI:

https://doi.org/10.33393/dti.2008.1327

Keywords:

folate receptor, gallium, DOTA, targeting, cytotoxicity

Abstract

The development of gallium(III) compounds as anti-cancer agents for both treatment and diagnosis is a rapidly developing field of research. Problems remain in exploring the full potential of gallium(III) as a safe and successful therapeutic agent or as an imaging agent. One of the major issues is that gallium(III) compounds have little tropism for cancer cells. We have combined the targeting properties of folic acid (FA) with long chain liquid polymer poly(ethylene glycol) (PEG) ‘spacers’. This FA-PEG unit has been coupled to the gallium coordination complex of 1,4,7,10-tetraazacyclo-dodecane-N,N',N",N"'-tetraacetic acid (DOTA) through amide linkages for delivery into target cells overexpressing the folate receptor (FR). In vitro cytotoxicity assays were conducted against a multi-drug resistant ovarian cell line (A2780/AD) that overexpresses the FR and contrasted against a FR free Chinese hamster ovary (CHO) cell line. Results are rationalized taking into account stability studies conducted in RPMI 1640 media and HEPES buffer at pH 7.4.

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Published

2008-03-01

How to Cite

Viola-Villegas, N., Vortherms, A., & Doyle, R. P. (2008). Targeting Gallium to Cancer Cells through the Folate Receptor. Drug Target Insights, 3(1). https://doi.org/10.33393/dti.2008.1327

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Original Research Article

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