Flaxseed and its lignan and oil components reduce mammary tumor growth at a late stage of carcinogenesis

Flaxseed, a rich source of mammalian lignan precursor secoisolariciresinol-diglycoside (S.D.) and alpha-linolenic acid (ALA), has been shown to be protective at the early promotion stage of carcinogenesis. The objective of this study was to determine whether supplementation with flaxseed, its lignan...

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Veröffentlicht in:Carcinogenesis (New York) 1996-06, Vol.17 (6), p.1373-1376
Hauptverfasser: THOMPSON, L. U, RICKARD, S. E, ORCHESON, L. J, SEIDL, M. M
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RICKARD, S. E
ORCHESON, L. J
SEIDL, M. M
description Flaxseed, a rich source of mammalian lignan precursor secoisolariciresinol-diglycoside (S.D.) and alpha-linolenic acid (ALA), has been shown to be protective at the early promotion stage of carcinogenesis. The objective of this study was to determine whether supplementation with flaxseed, its lignan or oil fractions, beginning 13 weeks after carcinogen administration, would reduce the size of established mammary tumors (present at the start of treatment) and appearance of new tumors in rats. Dietary groups consisted of the basal diet (BD, 20% corn oil) alone or supplemented with a gavage of 2200 nmol/day S.D. [S.D., equal to level in 5% flaxseed (F)], 1.82% flaxseed oil (OIL, equal to level in 5% F) or 2.5% or 5% flaxseed (2.5% F and 5% F, respectively). After 7 weeks of treatment, established tumor volume was over 50% smaller in all treatment groups (OIL, 2.5% F, 5% F, P < 0.04; S.D., P < 0.08) while there was no change in the BD group. New tumor number and volume were lowest in the S.D. (P < 0.02) and 2.5% F (P < 0.07) groups. The combined established and new tumor volumes were smaller for the S.D., 2.5% F and 5% F groups (P < 0.02) compared to the OIL and BD groups. The high negative correlation (r = -0.997, P < 0.001) between established tumor volume and urinary mammalian lignan excretion in the BD, S.D., 2.5% F and 5% F groups indicates that the reduction in tumor size is due in part to the lignans derived from the S.D. in flaxseed. However, there was no relationship between new or total tumor development and urinary lignan levels. The effect of flaxseed oil may be related to its high ALA content. In conclusion, the S.D. in flaxseed appears to be beneficial throughout the promotional phase of carcinogenesis whereas the oil component is more effective at the stage when tumors have already been established.
doi_str_mv 10.1093/carcin/17.6.1373
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U</creatorcontrib><creatorcontrib>RICKARD, S. E</creatorcontrib><creatorcontrib>ORCHESON, L. J</creatorcontrib><creatorcontrib>SEIDL, M. M</creatorcontrib><title>Flaxseed and its lignan and oil components reduce mammary tumor growth at a late stage of carcinogenesis</title><title>Carcinogenesis (New York)</title><addtitle>Carcinogenesis</addtitle><description><![CDATA[Flaxseed, a rich source of mammalian lignan precursor secoisolariciresinol-diglycoside (S.D.) and alpha-linolenic acid (ALA), has been shown to be protective at the early promotion stage of carcinogenesis. The objective of this study was to determine whether supplementation with flaxseed, its lignan or oil fractions, beginning 13 weeks after carcinogen administration, would reduce the size of established mammary tumors (present at the start of treatment) and appearance of new tumors in rats. Dietary groups consisted of the basal diet (BD, 20% corn oil) alone or supplemented with a gavage of 2200 nmol/day S.D. [S.D., equal to level in 5% flaxseed (F)], 1.82% flaxseed oil (OIL, equal to level in 5% F) or 2.5% or 5% flaxseed (2.5% F and 5% F, respectively). After 7 weeks of treatment, established tumor volume was over 50% smaller in all treatment groups (OIL, 2.5% F, 5% F, P < 0.04; S.D., P < 0.08) while there was no change in the BD group. New tumor number and volume were lowest in the S.D. (P < 0.02) and 2.5% F (P < 0.07) groups. The combined established and new tumor volumes were smaller for the S.D., 2.5% F and 5% F groups (P < 0.02) compared to the OIL and BD groups. The high negative correlation (r = -0.997, P < 0.001) between established tumor volume and urinary mammalian lignan excretion in the BD, S.D., 2.5% F and 5% F groups indicates that the reduction in tumor size is due in part to the lignans derived from the S.D. in flaxseed. However, there was no relationship between new or total tumor development and urinary lignan levels. 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Experimental tumors</subject><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Antineoplastic Agents, Phytogenic - urine</subject><subject>Biological and medical sciences</subject><subject>Butylene Glycols - pharmacology</subject><subject>Butylene Glycols - urine</subject><subject>Carcinogens</subject><subject>Cell Division - drug effects</subject><subject>Experimental genital and mammary tumors</subject><subject>Female</subject><subject>Glucosides - pharmacology</subject><subject>Glucosides - urine</subject><subject>Lignans - pharmacology</subject><subject>Lignans - urine</subject><subject>Mammary Neoplasms, Experimental - chemically induced</subject><subject>Mammary Neoplasms, Experimental - drug therapy</subject><subject>Mammary Neoplasms, Experimental - urine</subject><subject>Medical sciences</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Seeds</subject><subject>Tumors</subject><issn>0143-3334</issn><issn>1460-2180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9j8FLwzAYxYMoc07vXoQcvHZL-rVJepThVBh40fP42nzpKm1amgz1v3e64unx-D0e7zF2K8VSigJWFY5V41dSL9VSgoYzNpeZEkkqjThncyEzSAAgu2RXIXwIIRXkxYzNjDIyy82c7TctfgUiy9Fb3sTA26b26P9s37S86ruh9-SPZCR7qIh32HU4fvN46PqR12P_GfccI0feYiQeItbEe8dP2_qaPIUmXLMLh22gm0kX7H3z-LZ-TravTy_rh20ypJDHxOQARS6tUZo0ZbrMMnSObErkpFamKK0C0nkKpdFYKptakTsrlHAIVelgwe5OvcOh7MjuhrH5XbubHh_5_cQxVNi6EX3VhP8YyFQKLeAH0NFnmw</recordid><startdate>19960601</startdate><enddate>19960601</enddate><creator>THOMPSON, L. 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Experimental tumors</topic><topic>Animals</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Antineoplastic Agents, Phytogenic - urine</topic><topic>Biological and medical sciences</topic><topic>Butylene Glycols - pharmacology</topic><topic>Butylene Glycols - urine</topic><topic>Carcinogens</topic><topic>Cell Division - drug effects</topic><topic>Experimental genital and mammary tumors</topic><topic>Female</topic><topic>Glucosides - pharmacology</topic><topic>Glucosides - urine</topic><topic>Lignans - pharmacology</topic><topic>Lignans - urine</topic><topic>Mammary Neoplasms, Experimental - chemically induced</topic><topic>Mammary Neoplasms, Experimental - drug therapy</topic><topic>Mammary Neoplasms, Experimental - urine</topic><topic>Medical sciences</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Seeds</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>THOMPSON, L. U</creatorcontrib><creatorcontrib>RICKARD, S. E</creatorcontrib><creatorcontrib>ORCHESON, L. J</creatorcontrib><creatorcontrib>SEIDL, M. M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Carcinogenesis (New York)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>THOMPSON, L. U</au><au>RICKARD, S. E</au><au>ORCHESON, L. J</au><au>SEIDL, M. 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Dietary groups consisted of the basal diet (BD, 20% corn oil) alone or supplemented with a gavage of 2200 nmol/day S.D. [S.D., equal to level in 5% flaxseed (F)], 1.82% flaxseed oil (OIL, equal to level in 5% F) or 2.5% or 5% flaxseed (2.5% F and 5% F, respectively). After 7 weeks of treatment, established tumor volume was over 50% smaller in all treatment groups (OIL, 2.5% F, 5% F, P < 0.04; S.D., P < 0.08) while there was no change in the BD group. New tumor number and volume were lowest in the S.D. (P < 0.02) and 2.5% F (P < 0.07) groups. The combined established and new tumor volumes were smaller for the S.D., 2.5% F and 5% F groups (P < 0.02) compared to the OIL and BD groups. The high negative correlation (r = -0.997, P < 0.001) between established tumor volume and urinary mammalian lignan excretion in the BD, S.D., 2.5% F and 5% F groups indicates that the reduction in tumor size is due in part to the lignans derived from the S.D. in flaxseed. However, there was no relationship between new or total tumor development and urinary lignan levels. The effect of flaxseed oil may be related to its high ALA content. In conclusion, the S.D. in flaxseed appears to be beneficial throughout the promotional phase of carcinogenesis whereas the oil component is more effective at the stage when tumors have already been established.]]></abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>8681458</pmid><doi>10.1093/carcin/17.6.1373</doi><tpages>4</tpages></addata></record>
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ispartof Carcinogenesis (New York), 1996-06, Vol.17 (6), p.1373-1376
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Animal tumors. Experimental tumors
Animals
Antineoplastic Agents, Phytogenic - pharmacology
Antineoplastic Agents, Phytogenic - urine
Biological and medical sciences
Butylene Glycols - pharmacology
Butylene Glycols - urine
Carcinogens
Cell Division - drug effects
Experimental genital and mammary tumors
Female
Glucosides - pharmacology
Glucosides - urine
Lignans - pharmacology
Lignans - urine
Mammary Neoplasms, Experimental - chemically induced
Mammary Neoplasms, Experimental - drug therapy
Mammary Neoplasms, Experimental - urine
Medical sciences
Rats
Rats, Sprague-Dawley
Seeds
Tumors
title Flaxseed and its lignan and oil components reduce mammary tumor growth at a late stage of carcinogenesis
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