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...
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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 |
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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 & 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</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 & 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 & 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 & 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 & control</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - pathology</subject><subject>Neoplasms - prevention & 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 & 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 & 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 & 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 & control</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - pathology</topic><topic>Neoplasms - prevention & 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> |
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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 |
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