Zebularine: a unique molecule for an epigenetically based strategy in cancer chemotherapy.

Victor E. Marquez; James A. Kelley; Riad Agbaria; Tisipi Ben-Kasus; Jonathan C. Cheng; Christine B. Yoo; Peter A. Jones

doi:10.1196/annals.1359.037

Zebularine: a unique molecule for an epigenetically based strategy in cancer chemotherapy.

Victor E. Marquez, James A. Kelley, Riad Agbaria, Tisipi Ben-Kasus, Jonathan C. Cheng, Christine B. Yoo, Peter A. Jones

Research output: Contribution to journal › Review article › peer-review

81 Scopus citations

Abstract

1-(Beta-d-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine) corresponds structurally to cytidine minus the exocyclic 4-amino group. The increased electrophilic character of its simple aglycon endows the molecule with unique biologic properties as a potent inhibitor of both cytidine deaminase and DNA cytosine methyltransferase. The latter activity makes zebularine a promising antitumor agent that is hydrolytically stable, preferentially targets cancer cells, and shows activity both in vitro and in experimental animals, even after oral administration.

Original language	English
Pages (from-to)	246-254
Number of pages	9
Journal	Annals of the New York Academy of Sciences
Volume	1058
DOIs	https://doi.org/10.1196/annals.1359.037
State	Published - 1 Jan 2005
Externally published	Yes

ASJC Scopus subject areas

General Neuroscience
General Biochemistry, Genetics and Molecular Biology
History and Philosophy of Science

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10.1196/annals.1359.037

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title = "Zebularine: a unique molecule for an epigenetically based strategy in cancer chemotherapy.",

abstract = "1-(Beta-d-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine) corresponds structurally to cytidine minus the exocyclic 4-amino group. The increased electrophilic character of its simple aglycon endows the molecule with unique biologic properties as a potent inhibitor of both cytidine deaminase and DNA cytosine methyltransferase. The latter activity makes zebularine a promising antitumor agent that is hydrolytically stable, preferentially targets cancer cells, and shows activity both in vitro and in experimental animals, even after oral administration.",

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T2 - a unique molecule for an epigenetically based strategy in cancer chemotherapy.

AU - Marquez, Victor E.

AU - Kelley, James A.

AU - Agbaria, Riad

AU - Ben-Kasus, Tisipi

AU - Cheng, Jonathan C.

AU - Yoo, Christine B.

AU - Jones, Peter A.

PY - 2005/1/1

Y1 - 2005/1/1

N2 - 1-(Beta-d-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine) corresponds structurally to cytidine minus the exocyclic 4-amino group. The increased electrophilic character of its simple aglycon endows the molecule with unique biologic properties as a potent inhibitor of both cytidine deaminase and DNA cytosine methyltransferase. The latter activity makes zebularine a promising antitumor agent that is hydrolytically stable, preferentially targets cancer cells, and shows activity both in vitro and in experimental animals, even after oral administration.

AB - 1-(Beta-d-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine) corresponds structurally to cytidine minus the exocyclic 4-amino group. The increased electrophilic character of its simple aglycon endows the molecule with unique biologic properties as a potent inhibitor of both cytidine deaminase and DNA cytosine methyltransferase. The latter activity makes zebularine a promising antitumor agent that is hydrolytically stable, preferentially targets cancer cells, and shows activity both in vitro and in experimental animals, even after oral administration.

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U2 - 10.1196/annals.1359.037

DO - 10.1196/annals.1359.037

M3 - Review article

AN - SCOPUS:33745312816

SN - 0077-8923

VL - 1058

SP - 246

EP - 254

JO - Annals of the New York Academy of Sciences

JF - Annals of the New York Academy of Sciences

ER -

Zebularine: a unique molecule for an epigenetically based strategy in cancer chemotherapy.

Abstract

ASJC Scopus subject areas

UN SDGs

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