Effect of the Synthetic Pineal Peptide Epitalon on Spontaneous Carcinogenesis in Female C3H/He Mice

The potential preventive effect of the synthetic pineal peptide Epitalon® (Ala-Glu-Asp-Gly) on spontaneous tumorigenesis in mice was studied. One-year-old female C3H/He mice were kept for 6.5 months under standard conditions. Epitalon was injected at a dose of 0.1 μg, 5 times a week. Long-term exp...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:In vivo (Athens) 2006-03, Vol.20 (2), p.253
Hauptverfasser: GEORGE KOSSOY, VLADIMIR N. ANISIMOV, HERZEL BEN-HUR, NADJA KOSSOY, ITSHAK ZUSMAN
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 2
container_start_page 253
container_title In vivo (Athens)
container_volume 20
creator GEORGE KOSSOY
VLADIMIR N. ANISIMOV
HERZEL BEN-HUR
NADJA KOSSOY
ITSHAK ZUSMAN
description The potential preventive effect of the synthetic pineal peptide Epitalon® (Ala-Glu-Asp-Gly) on spontaneous tumorigenesis in mice was studied. One-year-old female C3H/He mice were kept for 6.5 months under standard conditions. Epitalon was injected at a dose of 0.1 μg, 5 times a week. Long-term exposure to Epitalon in small doses did not show any toxic effect. Treatment with Epitalon decreased the number of tumor-bearing mice with malignant tumors and prevented the development of metastases. Spontaneous tumors of the reproductive organs (mammary glands and ovaries) were predominant in both groups of mice (control and experimental). The mammary gland tumors were different variants of invasive ductal carcinomas. In the ovaries, granulosa-cell tumors were found. Tumors were in the minority in other organs and had benign characteristics. In control mice, metastases were found in 3 out of 9 tumor-bearing mice, all of them being from tumors of the reproductive organs. Treatment with Epitalon slowed down the development of metastases from spontaneous tumors, and no metastases were found in the experimental mice. These data highlight the antimetastatic effect of Epitalon as part of its oncostatic properties.
format Article
fullrecord <record><control><sourceid>pubmed_highw</sourceid><recordid>TN_cdi_pubmed_primary_16634527</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>16634527</sourcerecordid><originalsourceid>FETCH-LOGICAL-h238t-3c63acb6823bee922539b63f110f68434958fbece52f12996aca23a0fecf7ed53</originalsourceid><addsrcrecordid>eNo1j11LwzAYhYMobk7_guTC22I-mrS5lLI5YeJgCt6VNH2zRrq0NJmyf29gCgfOzcP5uEBzWiiaFSJXl2hOmCizUtDPGboJ4YsQWRDCrtGMSslzwYo5MktrwUQ8WBw7wLuTTxadwVvnQfd4C2N0LeDl6KLuB4-TduPgo_YwHAOu9GScH_bgIbiAnccrOOgecMXXj2vAr87ALbqyug9w9-cL9LFavlfrbPP2_FI9bbKO8TJm3EiuTSNLxhsAxZjgqpHcUkqsLHOeK1HaBgwIZilTSmqjGdck7bcFtIIv0P05dzw2B2jrcXIHPZ3q_7cJeDgDndt3P26COqStfcJ57b4ZqVmdSvkvR2lenQ</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Effect of the Synthetic Pineal Peptide Epitalon on Spontaneous Carcinogenesis in Female C3H/He Mice</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>GEORGE KOSSOY ; VLADIMIR N. ANISIMOV ; HERZEL BEN-HUR ; NADJA KOSSOY ; ITSHAK ZUSMAN</creator><creatorcontrib>GEORGE KOSSOY ; VLADIMIR N. ANISIMOV ; HERZEL BEN-HUR ; NADJA KOSSOY ; ITSHAK ZUSMAN</creatorcontrib><description>The potential preventive effect of the synthetic pineal peptide Epitalon® (Ala-Glu-Asp-Gly) on spontaneous tumorigenesis in mice was studied. One-year-old female C3H/He mice were kept for 6.5 months under standard conditions. Epitalon was injected at a dose of 0.1 μg, 5 times a week. Long-term exposure to Epitalon in small doses did not show any toxic effect. Treatment with Epitalon decreased the number of tumor-bearing mice with malignant tumors and prevented the development of metastases. Spontaneous tumors of the reproductive organs (mammary glands and ovaries) were predominant in both groups of mice (control and experimental). The mammary gland tumors were different variants of invasive ductal carcinomas. In the ovaries, granulosa-cell tumors were found. Tumors were in the minority in other organs and had benign characteristics. In control mice, metastases were found in 3 out of 9 tumor-bearing mice, all of them being from tumors of the reproductive organs. Treatment with Epitalon slowed down the development of metastases from spontaneous tumors, and no metastases were found in the experimental mice. These data highlight the antimetastatic effect of Epitalon as part of its oncostatic properties.</description><identifier>ISSN: 0258-851X</identifier><identifier>EISSN: 1791-7549</identifier><identifier>PMID: 16634527</identifier><language>eng</language><publisher>Greece: International Institute of Anticancer Research</publisher><subject>Animals ; Antineoplastic Agents - pharmacology ; Carcinoma, Intraductal, Noninfiltrating - drug therapy ; Carcinoma, Intraductal, Noninfiltrating - prevention &amp; control ; Carcinoma, Intraductal, Noninfiltrating - secondary ; Drug Screening Assays, Antitumor ; Female ; Lung Neoplasms - drug therapy ; Lung Neoplasms - prevention &amp; control ; Lung Neoplasms - secondary ; Mammary Neoplasms, Animal - drug therapy ; Mammary Neoplasms, Animal - pathology ; Mammary Neoplasms, Animal - prevention &amp; control ; Mice ; Mice, Inbred C3H ; Neoplasm Metastasis - drug therapy ; Neoplasm Metastasis - pathology ; Neoplasm Metastasis - prevention &amp; control ; Neoplasms - drug therapy ; Neoplasms - pathology ; Neoplasms - prevention &amp; control ; Oligopeptides - pharmacology</subject><ispartof>In vivo (Athens), 2006-03, Vol.20 (2), p.253</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16634527$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GEORGE KOSSOY</creatorcontrib><creatorcontrib>VLADIMIR N. ANISIMOV</creatorcontrib><creatorcontrib>HERZEL BEN-HUR</creatorcontrib><creatorcontrib>NADJA KOSSOY</creatorcontrib><creatorcontrib>ITSHAK ZUSMAN</creatorcontrib><title>Effect of the Synthetic Pineal Peptide Epitalon on Spontaneous Carcinogenesis in Female C3H/He Mice</title><title>In vivo (Athens)</title><addtitle>In Vivo</addtitle><description>The potential preventive effect of the synthetic pineal peptide Epitalon® (Ala-Glu-Asp-Gly) on spontaneous tumorigenesis in mice was studied. One-year-old female C3H/He mice were kept for 6.5 months under standard conditions. Epitalon was injected at a dose of 0.1 μg, 5 times a week. Long-term exposure to Epitalon in small doses did not show any toxic effect. Treatment with Epitalon decreased the number of tumor-bearing mice with malignant tumors and prevented the development of metastases. Spontaneous tumors of the reproductive organs (mammary glands and ovaries) were predominant in both groups of mice (control and experimental). The mammary gland tumors were different variants of invasive ductal carcinomas. In the ovaries, granulosa-cell tumors were found. Tumors were in the minority in other organs and had benign characteristics. In control mice, metastases were found in 3 out of 9 tumor-bearing mice, all of them being from tumors of the reproductive organs. Treatment with Epitalon slowed down the development of metastases from spontaneous tumors, and no metastases were found in the experimental mice. These data highlight the antimetastatic effect of Epitalon as part of its oncostatic properties.</description><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Carcinoma, Intraductal, Noninfiltrating - drug therapy</subject><subject>Carcinoma, Intraductal, Noninfiltrating - prevention &amp; control</subject><subject>Carcinoma, Intraductal, Noninfiltrating - secondary</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Female</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - prevention &amp; control</subject><subject>Lung Neoplasms - secondary</subject><subject>Mammary Neoplasms, Animal - drug therapy</subject><subject>Mammary Neoplasms, Animal - pathology</subject><subject>Mammary Neoplasms, Animal - prevention &amp; control</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Neoplasm Metastasis - drug therapy</subject><subject>Neoplasm Metastasis - pathology</subject><subject>Neoplasm Metastasis - prevention &amp; control</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - pathology</subject><subject>Neoplasms - prevention &amp; control</subject><subject>Oligopeptides - pharmacology</subject><issn>0258-851X</issn><issn>1791-7549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j11LwzAYhYMobk7_guTC22I-mrS5lLI5YeJgCt6VNH2zRrq0NJmyf29gCgfOzcP5uEBzWiiaFSJXl2hOmCizUtDPGboJ4YsQWRDCrtGMSslzwYo5MktrwUQ8WBw7wLuTTxadwVvnQfd4C2N0LeDl6KLuB4-TduPgo_YwHAOu9GScH_bgIbiAnccrOOgecMXXj2vAr87ALbqyug9w9-cL9LFavlfrbPP2_FI9bbKO8TJm3EiuTSNLxhsAxZjgqpHcUkqsLHOeK1HaBgwIZilTSmqjGdck7bcFtIIv0P05dzw2B2jrcXIHPZ3q_7cJeDgDndt3P26COqStfcJ57b4ZqVmdSvkvR2lenQ</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>GEORGE KOSSOY</creator><creator>VLADIMIR N. ANISIMOV</creator><creator>HERZEL BEN-HUR</creator><creator>NADJA KOSSOY</creator><creator>ITSHAK ZUSMAN</creator><general>International Institute of Anticancer Research</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20060301</creationdate><title>Effect of the Synthetic Pineal Peptide Epitalon on Spontaneous Carcinogenesis in Female C3H/He Mice</title><author>GEORGE KOSSOY ; VLADIMIR N. ANISIMOV ; HERZEL BEN-HUR ; NADJA KOSSOY ; ITSHAK ZUSMAN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h238t-3c63acb6823bee922539b63f110f68434958fbece52f12996aca23a0fecf7ed53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Carcinoma, Intraductal, Noninfiltrating - drug therapy</topic><topic>Carcinoma, Intraductal, Noninfiltrating - prevention &amp; control</topic><topic>Carcinoma, Intraductal, Noninfiltrating - secondary</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Female</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - prevention &amp; control</topic><topic>Lung Neoplasms - secondary</topic><topic>Mammary Neoplasms, Animal - drug therapy</topic><topic>Mammary Neoplasms, Animal - pathology</topic><topic>Mammary Neoplasms, Animal - prevention &amp; control</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Neoplasm Metastasis - drug therapy</topic><topic>Neoplasm Metastasis - pathology</topic><topic>Neoplasm Metastasis - prevention &amp; control</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - pathology</topic><topic>Neoplasms - prevention &amp; control</topic><topic>Oligopeptides - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GEORGE KOSSOY</creatorcontrib><creatorcontrib>VLADIMIR N. ANISIMOV</creatorcontrib><creatorcontrib>HERZEL BEN-HUR</creatorcontrib><creatorcontrib>NADJA KOSSOY</creatorcontrib><creatorcontrib>ITSHAK ZUSMAN</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>In vivo (Athens)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GEORGE KOSSOY</au><au>VLADIMIR N. ANISIMOV</au><au>HERZEL BEN-HUR</au><au>NADJA KOSSOY</au><au>ITSHAK ZUSMAN</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of the Synthetic Pineal Peptide Epitalon on Spontaneous Carcinogenesis in Female C3H/He Mice</atitle><jtitle>In vivo (Athens)</jtitle><addtitle>In Vivo</addtitle><date>2006-03-01</date><risdate>2006</risdate><volume>20</volume><issue>2</issue><spage>253</spage><pages>253-</pages><issn>0258-851X</issn><eissn>1791-7549</eissn><abstract>The potential preventive effect of the synthetic pineal peptide Epitalon® (Ala-Glu-Asp-Gly) on spontaneous tumorigenesis in mice was studied. One-year-old female C3H/He mice were kept for 6.5 months under standard conditions. Epitalon was injected at a dose of 0.1 μg, 5 times a week. Long-term exposure to Epitalon in small doses did not show any toxic effect. Treatment with Epitalon decreased the number of tumor-bearing mice with malignant tumors and prevented the development of metastases. Spontaneous tumors of the reproductive organs (mammary glands and ovaries) were predominant in both groups of mice (control and experimental). The mammary gland tumors were different variants of invasive ductal carcinomas. In the ovaries, granulosa-cell tumors were found. Tumors were in the minority in other organs and had benign characteristics. In control mice, metastases were found in 3 out of 9 tumor-bearing mice, all of them being from tumors of the reproductive organs. Treatment with Epitalon slowed down the development of metastases from spontaneous tumors, and no metastases were found in the experimental mice. These data highlight the antimetastatic effect of Epitalon as part of its oncostatic properties.</abstract><cop>Greece</cop><pub>International Institute of Anticancer Research</pub><pmid>16634527</pmid></addata></record>
fulltext fulltext
identifier ISSN: 0258-851X
ispartof In vivo (Athens), 2006-03, Vol.20 (2), p.253
issn 0258-851X
1791-7549
language eng
recordid cdi_pubmed_primary_16634527
source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Animals
Antineoplastic Agents - pharmacology
Carcinoma, Intraductal, Noninfiltrating - drug therapy
Carcinoma, Intraductal, Noninfiltrating - prevention & control
Carcinoma, Intraductal, Noninfiltrating - secondary
Drug Screening Assays, Antitumor
Female
Lung Neoplasms - drug therapy
Lung Neoplasms - prevention & control
Lung Neoplasms - secondary
Mammary Neoplasms, Animal - drug therapy
Mammary Neoplasms, Animal - pathology
Mammary Neoplasms, Animal - prevention & control
Mice
Mice, Inbred C3H
Neoplasm Metastasis - drug therapy
Neoplasm Metastasis - pathology
Neoplasm Metastasis - prevention & control
Neoplasms - drug therapy
Neoplasms - pathology
Neoplasms - prevention & control
Oligopeptides - pharmacology
title Effect of the Synthetic Pineal Peptide Epitalon on Spontaneous Carcinogenesis in Female C3H/He Mice
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T12%3A27%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_highw&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effect%20of%20the%20Synthetic%20Pineal%20Peptide%20Epitalon%20on%20Spontaneous%20Carcinogenesis%20in%20Female%20C3H/He%20Mice&rft.jtitle=In%20vivo%20(Athens)&rft.au=GEORGE%20KOSSOY&rft.date=2006-03-01&rft.volume=20&rft.issue=2&rft.spage=253&rft.pages=253-&rft.issn=0258-851X&rft.eissn=1791-7549&rft_id=info:doi/&rft_dat=%3Cpubmed_highw%3E16634527%3C/pubmed_highw%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/16634527&rfr_iscdi=true