Loading…
Melatonin, environmental light, and breast cancer
Although many factors have been suggested as causes for breast cancer, the increased incidence of the disease seen in women working in night shifts led to the hypothesis that the suppression of melatonin by light or melatonin deficiency plays a major role in cancer development. Studies on the 7,12-d...
Saved in:
Published in: | Breast cancer research and treatment 2008-04, Vol.108 (3), p.339-350 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c430t-30f61f2a5f2bc0fcb95b23f27a52c9dd099e1efb91dad21e37021b10dab47f13 |
---|---|
cites | cdi_FETCH-LOGICAL-c430t-30f61f2a5f2bc0fcb95b23f27a52c9dd099e1efb91dad21e37021b10dab47f13 |
container_end_page | 350 |
container_issue | 3 |
container_start_page | 339 |
container_title | Breast cancer research and treatment |
container_volume | 108 |
creator | Srinivasan, V. Spence, D. W. Pandi-Perumal, S. R. Trakht, I. Esquifino, A. I. Cardinali, D. P. Maestroni, G. J. |
description | Although many factors have been suggested as causes for breast cancer, the increased incidence of the disease seen in women working in night shifts led to the hypothesis that the suppression of melatonin by light or melatonin deficiency plays a major role in cancer development. Studies on the 7,12-dimethylbenz[a]anthracene and
N
-methyl-
N
-nitrosourea experimental models of human breast cancer indicate that melatonin is effective in reducing cancer development. In vitro studies in MCF-7 human breast cancer cell line have shown that melatonin exerts its anticarcinogenic actions through a variety of mechanisms, and that it is most effective in estrogen receptor (ER) α-positive breast cancer cells. Melatonin suppresses ER gene, modulates several estrogen dependent regulatory proteins and pro-oncogenes, inhibits cell proliferation, and impairs the metastatic capacity of MCF-7 human breast cancer cells. The anticarcinogenic action on MCF-7 cells has been demonstrated at the physiological concentrations of melatonin attained at night, suggesting thereby that melatonin acts like an endogenous antiestrogen. Melatonin also decreases the formation of estrogens from androgens via aromatase inhibition. Circulating melatonin levels are abnormally low in ER-positive breast cancer patients thereby supporting the melatonin hypothesis for breast cancer in shift working women. It has been postulated that enhanced endogenous melatonin secretion is responsible for the beneficial effects of meditation as a form of psychosocial intervention that helps breast cancer patients. |
doi_str_mv | 10.1007/s10549-007-9617-5 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_20781311</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1453039771</sourcerecordid><originalsourceid>FETCH-LOGICAL-c430t-30f61f2a5f2bc0fcb95b23f27a52c9dd099e1efb91dad21e37021b10dab47f13</originalsourceid><addsrcrecordid>eNp1kN9LwzAQx4Mobk7_AF-kCPq06l3SNs2jDH_BxJe9hzRNZkebzqQV_O9t2XAg-JSDfO57dx9CLhHuEIDfB4Q0EfFQxiJDHqdHZIopZzGnyI_JFDDjcZZDNiFnIWwAQHAQp2SCPE2QMzEl-GZq1bWucvPIuK_Kt64xrlN1VFfrj24eKVdGhTcqdJFWTht_Tk6sqoO52L8zsnp6XC1e4uX78-viYRnrhEEXM7AZWqpSSwsNVhciLSizlKuUalGWIIRBYwuBpSopGsaBYoFQqiLhFtmM3O5it7797E3oZFMFbepaOdP2QVLgOTIcwes_4KbtvRtWkxRpkgma5AOEO0j7NgRvrNz6qlH-WyLI0aXcuZRjObqU6dBztQ_ui8aUh469vAG42QMqaFVbP_ipwi9Hh4PynI1BdMeF4cutjT9s-P_0H_1rim4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>212469248</pqid></control><display><type>article</type><title>Melatonin, environmental light, and breast cancer</title><source>Springer Nature</source><creator>Srinivasan, V. ; Spence, D. W. ; Pandi-Perumal, S. R. ; Trakht, I. ; Esquifino, A. I. ; Cardinali, D. P. ; Maestroni, G. J.</creator><creatorcontrib>Srinivasan, V. ; Spence, D. W. ; Pandi-Perumal, S. R. ; Trakht, I. ; Esquifino, A. I. ; Cardinali, D. P. ; Maestroni, G. J.</creatorcontrib><description>Although many factors have been suggested as causes for breast cancer, the increased incidence of the disease seen in women working in night shifts led to the hypothesis that the suppression of melatonin by light or melatonin deficiency plays a major role in cancer development. Studies on the 7,12-dimethylbenz[a]anthracene and
N
-methyl-
N
-nitrosourea experimental models of human breast cancer indicate that melatonin is effective in reducing cancer development. In vitro studies in MCF-7 human breast cancer cell line have shown that melatonin exerts its anticarcinogenic actions through a variety of mechanisms, and that it is most effective in estrogen receptor (ER) α-positive breast cancer cells. Melatonin suppresses ER gene, modulates several estrogen dependent regulatory proteins and pro-oncogenes, inhibits cell proliferation, and impairs the metastatic capacity of MCF-7 human breast cancer cells. The anticarcinogenic action on MCF-7 cells has been demonstrated at the physiological concentrations of melatonin attained at night, suggesting thereby that melatonin acts like an endogenous antiestrogen. Melatonin also decreases the formation of estrogens from androgens via aromatase inhibition. Circulating melatonin levels are abnormally low in ER-positive breast cancer patients thereby supporting the melatonin hypothesis for breast cancer in shift working women. It has been postulated that enhanced endogenous melatonin secretion is responsible for the beneficial effects of meditation as a form of psychosocial intervention that helps breast cancer patients.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-007-9617-5</identifier><identifier>PMID: 17541739</identifier><identifier>CODEN: BCTRD6</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Biological and medical sciences ; Breast cancer ; Breast Neoplasms - etiology ; Breast Neoplasms - physiopathology ; Cancer research ; Cancer therapies ; Circadian Rhythm - physiology ; Female ; Gynecology. Andrology. Obstetrics ; Hormones ; Humans ; Light ; Lighting - adverse effects ; Mammary gland diseases ; Medical sciences ; Medicine ; Medicine & Public Health ; Melatonin - physiology ; Occupational Exposure - adverse effects ; Oncology ; Pathology ; Review ; Tumors</subject><ispartof>Breast cancer research and treatment, 2008-04, Vol.108 (3), p.339-350</ispartof><rights>Springer Science+Business Media, LLC 2007</rights><rights>2008 INIST-CNRS</rights><rights>Springer Science+Business Media, LLC. 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-30f61f2a5f2bc0fcb95b23f27a52c9dd099e1efb91dad21e37021b10dab47f13</citedby><cites>FETCH-LOGICAL-c430t-30f61f2a5f2bc0fcb95b23f27a52c9dd099e1efb91dad21e37021b10dab47f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20218835$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17541739$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Srinivasan, V.</creatorcontrib><creatorcontrib>Spence, D. W.</creatorcontrib><creatorcontrib>Pandi-Perumal, S. R.</creatorcontrib><creatorcontrib>Trakht, I.</creatorcontrib><creatorcontrib>Esquifino, A. I.</creatorcontrib><creatorcontrib>Cardinali, D. P.</creatorcontrib><creatorcontrib>Maestroni, G. J.</creatorcontrib><title>Melatonin, environmental light, and breast cancer</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Although many factors have been suggested as causes for breast cancer, the increased incidence of the disease seen in women working in night shifts led to the hypothesis that the suppression of melatonin by light or melatonin deficiency plays a major role in cancer development. Studies on the 7,12-dimethylbenz[a]anthracene and
N
-methyl-
N
-nitrosourea experimental models of human breast cancer indicate that melatonin is effective in reducing cancer development. In vitro studies in MCF-7 human breast cancer cell line have shown that melatonin exerts its anticarcinogenic actions through a variety of mechanisms, and that it is most effective in estrogen receptor (ER) α-positive breast cancer cells. Melatonin suppresses ER gene, modulates several estrogen dependent regulatory proteins and pro-oncogenes, inhibits cell proliferation, and impairs the metastatic capacity of MCF-7 human breast cancer cells. The anticarcinogenic action on MCF-7 cells has been demonstrated at the physiological concentrations of melatonin attained at night, suggesting thereby that melatonin acts like an endogenous antiestrogen. Melatonin also decreases the formation of estrogens from androgens via aromatase inhibition. Circulating melatonin levels are abnormally low in ER-positive breast cancer patients thereby supporting the melatonin hypothesis for breast cancer in shift working women. It has been postulated that enhanced endogenous melatonin secretion is responsible for the beneficial effects of meditation as a form of psychosocial intervention that helps breast cancer patients.</description><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - etiology</subject><subject>Breast Neoplasms - physiopathology</subject><subject>Cancer research</subject><subject>Cancer therapies</subject><subject>Circadian Rhythm - physiology</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Hormones</subject><subject>Humans</subject><subject>Light</subject><subject>Lighting - adverse effects</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Melatonin - physiology</subject><subject>Occupational Exposure - adverse effects</subject><subject>Oncology</subject><subject>Pathology</subject><subject>Review</subject><subject>Tumors</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kN9LwzAQx4Mobk7_AF-kCPq06l3SNs2jDH_BxJe9hzRNZkebzqQV_O9t2XAg-JSDfO57dx9CLhHuEIDfB4Q0EfFQxiJDHqdHZIopZzGnyI_JFDDjcZZDNiFnIWwAQHAQp2SCPE2QMzEl-GZq1bWucvPIuK_Kt64xrlN1VFfrj24eKVdGhTcqdJFWTht_Tk6sqoO52L8zsnp6XC1e4uX78-viYRnrhEEXM7AZWqpSSwsNVhciLSizlKuUalGWIIRBYwuBpSopGsaBYoFQqiLhFtmM3O5it7797E3oZFMFbepaOdP2QVLgOTIcwes_4KbtvRtWkxRpkgma5AOEO0j7NgRvrNz6qlH-WyLI0aXcuZRjObqU6dBztQ_ui8aUh469vAG42QMqaFVbP_ipwi9Hh4PynI1BdMeF4cutjT9s-P_0H_1rim4</recordid><startdate>20080401</startdate><enddate>20080401</enddate><creator>Srinivasan, V.</creator><creator>Spence, D. W.</creator><creator>Pandi-Perumal, S. R.</creator><creator>Trakht, I.</creator><creator>Esquifino, A. I.</creator><creator>Cardinali, D. P.</creator><creator>Maestroni, G. J.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7TK</scope></search><sort><creationdate>20080401</creationdate><title>Melatonin, environmental light, and breast cancer</title><author>Srinivasan, V. ; Spence, D. W. ; Pandi-Perumal, S. R. ; Trakht, I. ; Esquifino, A. I. ; Cardinali, D. P. ; Maestroni, G. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-30f61f2a5f2bc0fcb95b23f27a52c9dd099e1efb91dad21e37021b10dab47f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Biological and medical sciences</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - etiology</topic><topic>Breast Neoplasms - physiopathology</topic><topic>Cancer research</topic><topic>Cancer therapies</topic><topic>Circadian Rhythm - physiology</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Hormones</topic><topic>Humans</topic><topic>Light</topic><topic>Lighting - adverse effects</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Melatonin - physiology</topic><topic>Occupational Exposure - adverse effects</topic><topic>Oncology</topic><topic>Pathology</topic><topic>Review</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Srinivasan, V.</creatorcontrib><creatorcontrib>Spence, D. W.</creatorcontrib><creatorcontrib>Pandi-Perumal, S. R.</creatorcontrib><creatorcontrib>Trakht, I.</creatorcontrib><creatorcontrib>Esquifino, A. I.</creatorcontrib><creatorcontrib>Cardinali, D. P.</creatorcontrib><creatorcontrib>Maestroni, G. J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Neurosciences Abstracts</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Srinivasan, V.</au><au>Spence, D. W.</au><au>Pandi-Perumal, S. R.</au><au>Trakht, I.</au><au>Esquifino, A. I.</au><au>Cardinali, D. P.</au><au>Maestroni, G. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Melatonin, environmental light, and breast cancer</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2008-04-01</date><risdate>2008</risdate><volume>108</volume><issue>3</issue><spage>339</spage><epage>350</epage><pages>339-350</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><coden>BCTRD6</coden><abstract>Although many factors have been suggested as causes for breast cancer, the increased incidence of the disease seen in women working in night shifts led to the hypothesis that the suppression of melatonin by light or melatonin deficiency plays a major role in cancer development. Studies on the 7,12-dimethylbenz[a]anthracene and
N
-methyl-
N
-nitrosourea experimental models of human breast cancer indicate that melatonin is effective in reducing cancer development. In vitro studies in MCF-7 human breast cancer cell line have shown that melatonin exerts its anticarcinogenic actions through a variety of mechanisms, and that it is most effective in estrogen receptor (ER) α-positive breast cancer cells. Melatonin suppresses ER gene, modulates several estrogen dependent regulatory proteins and pro-oncogenes, inhibits cell proliferation, and impairs the metastatic capacity of MCF-7 human breast cancer cells. The anticarcinogenic action on MCF-7 cells has been demonstrated at the physiological concentrations of melatonin attained at night, suggesting thereby that melatonin acts like an endogenous antiestrogen. Melatonin also decreases the formation of estrogens from androgens via aromatase inhibition. Circulating melatonin levels are abnormally low in ER-positive breast cancer patients thereby supporting the melatonin hypothesis for breast cancer in shift working women. It has been postulated that enhanced endogenous melatonin secretion is responsible for the beneficial effects of meditation as a form of psychosocial intervention that helps breast cancer patients.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>17541739</pmid><doi>10.1007/s10549-007-9617-5</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0167-6806 |
ispartof | Breast cancer research and treatment, 2008-04, Vol.108 (3), p.339-350 |
issn | 0167-6806 1573-7217 |
language | eng |
recordid | cdi_proquest_miscellaneous_20781311 |
source | Springer Nature |
subjects | Biological and medical sciences Breast cancer Breast Neoplasms - etiology Breast Neoplasms - physiopathology Cancer research Cancer therapies Circadian Rhythm - physiology Female Gynecology. Andrology. Obstetrics Hormones Humans Light Lighting - adverse effects Mammary gland diseases Medical sciences Medicine Medicine & Public Health Melatonin - physiology Occupational Exposure - adverse effects Oncology Pathology Review Tumors |
title | Melatonin, environmental light, and breast cancer |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T17%3A15%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Melatonin,%20environmental%20light,%20and%20breast%20cancer&rft.jtitle=Breast%20cancer%20research%20and%20treatment&rft.au=Srinivasan,%20V.&rft.date=2008-04-01&rft.volume=108&rft.issue=3&rft.spage=339&rft.epage=350&rft.pages=339-350&rft.issn=0167-6806&rft.eissn=1573-7217&rft.coden=BCTRD6&rft_id=info:doi/10.1007/s10549-007-9617-5&rft_dat=%3Cproquest_cross%3E1453039771%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c430t-30f61f2a5f2bc0fcb95b23f27a52c9dd099e1efb91dad21e37021b10dab47f13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=212469248&rft_id=info:pmid/17541739&rfr_iscdi=true |