Pathobiology

 

Inhibition of Mammary Carcinoma Growth by Retinoidal Benzoic Acid Derivatives

Fontana J.A.a · Hobbs P.D.b · Dawson I.b

Author affiliations

aUniversity of Maryland Cancer Center and Department of Medicine, University of Maryland, Baltimore, Md., and bLife Sciences Division, SRI International, Menlo Park, Calif., USA

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Expl Cell Biol 1988;56:254–263

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Article / Publication Details

First-Page Preview
Abstract of Paper

Received: March 29, 1988
Accepted: May 16, 1988
Published online: October 07, 2008
Issue release date: 1988

Number of Print Pages: 10
Number of Figures: 0
Number of Tables: 0

ISSN: 1015-2008 (Print)
eISSN: 1423-0291 (Online)

For additional information: https://www.karger.com/PAT

Abstract

The growth of many breast carcinoma cell lines is inhibited by vitamin A, and derivatives as well as synthetic retinoids. New retinoidal derivatives have recently been synthesized. These retinoidal benzoic acid derivatives displayed enhanced potency in their ability to reverse hamster tracheal keratinization and inhibit ornithine decarboxylase induction in mouse epidermis. We therefore screened a series of analogues of these compounds for their ability to inhibit human breast carcinoma cell proliferation utilizing three estrogen receptor-positive and two estrogen receptor-negative cell lines. The compound (E)-4–2-(5,6,7,8)tetrahydro-5,5,8,8-tetramethyl-2-naphtalenyl)propenyl benzoic acid (Ro 1374–10) was approximately 2–3 orders of magnitude more potent than all-trans-retinoic acid in inhibiting breast carcinoma cell proliferation while the compound SRI-6409–40, which differs from Ro 1374–10 only by the position of a methyl group, was 50-fold more potent than Ro 1374–10. All of the compounds tested displayed were inactive against the estrogen receptor-negative breast carcinoma lines.

© 1988 S. Karger AG, Basel




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Article / Publication Details

First-Page Preview
Abstract of Paper

Received: March 29, 1988
Accepted: May 16, 1988
Published online: October 07, 2008
Issue release date: 1988

Number of Print Pages: 10
Number of Figures: 0
Number of Tables: 0

ISSN: 1015-2008 (Print)
eISSN: 1423-0291 (Online)

For additional information: https://www.karger.com/PAT


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