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Synthesis and characterization of bioactive tamoxifen-conjugated polymers.


ABSTRACT: Macromolecular conjugates of tamoxifen could perhaps be used to circumvent some of the limitations of the extensively used breast cancer drug. To test the feasibility of these conjugates, a 4-hydroxytamoxifen analogue was conjugated to a diaminoalkyl linker and then conjugated to activated esters of a poly(methacrylic acid) polymer synthesized by atom transfer radical polymerization. A polymer conjugated to the 4-hydroxytamoxifen analogue with a six-carbon linker showed high affinity for both estrogen receptor alpha and estrogen receptor beta and potent antagonism of the estrogen receptor in cell-based transcriptional reporter assays. These results suggest that the conjugation of 4-hydroxytamoxifen to a polymer results in a macromolecular conjugate that can display ligand in a manner that can be recognized by estrogen receptor and still act as a potent antiestrogen in cells.

SUBMITTER: Rickert EL 

PROVIDER: S-EPMC2528197 | biostudies-literature | 2007 Nov

REPOSITORIES: biostudies-literature

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Synthesis and characterization of bioactive tamoxifen-conjugated polymers.

Rickert Emily L EL   Trebley Joseph P JP   Peterson Anton C AC   Morrell Melinda M MM   Weatherman Ross V RV  

Biomacromolecules 20071012 11


Macromolecular conjugates of tamoxifen could perhaps be used to circumvent some of the limitations of the extensively used breast cancer drug. To test the feasibility of these conjugates, a 4-hydroxytamoxifen analogue was conjugated to a diaminoalkyl linker and then conjugated to activated esters of a poly(methacrylic acid) polymer synthesized by atom transfer radical polymerization. A polymer conjugated to the 4-hydroxytamoxifen analogue with a six-carbon linker showed high affinity for both es  ...[more]

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