Membrane-bound estrogen receptor alpha initiated signaling is dynamin dependent in breast cancer cells.
Identifieur interne : 000876 ( PubMed/Corpus ); précédent : 000875; suivant : 000877Membrane-bound estrogen receptor alpha initiated signaling is dynamin dependent in breast cancer cells.
Auteurs : Istvan Marczell ; Petra Balogh ; Gabor Nyiro ; Anna L. Kiss ; Balazs Kovacs ; Gabor Bekesi ; Karoly Racz ; Attila PatocsSource :
- European journal of medical research [ 2047-783X ] ; 2018.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Dynamins, Estrogen Receptor alpha.
- metabolism : Breast Neoplasms, Cell Membrane.
- physiology : Signal Transduction.
- Female, Humans, MCF-7 Cells.
Abstract
Although membrane-associated estrogen receptors (mERs) have been known to play important role in steroid-induced signal transmission, we still know little about their function in the estrogen-induced proliferation of breast cancer cells.
DOI: 10.1186/s40001-018-0328-7
PubMed: 29880033
Links to Exploration step
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Kiss</name><affiliation><nlm:affiliation>Department of Human Morphology and Developmental Biology, Semmelweis University, Budapest, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Kovacs, Balazs" sort="Kovacs, Balazs" uniqKey="Kovacs B" first="Balazs" last="Kovacs">Balazs Kovacs</name><affiliation><nlm:affiliation>Department of Aquaculture, Szent Istvan University, Godollo, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Bekesi, Gabor" sort="Bekesi, Gabor" uniqKey="Bekesi G" first="Gabor" last="Bekesi">Gabor Bekesi</name><affiliation><nlm:affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Racz, Karoly" sort="Racz, Karoly" uniqKey="Racz K" first="Karoly" last="Racz">Karoly Racz</name><affiliation><nlm:affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Patocs, Attila" sort="Patocs, Attila" uniqKey="Patocs A" first="Attila" last="Patocs">Attila Patocs</name><affiliation><nlm:affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary. patocs.attila@med.semmelweis-univ.hu.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2018">2018</date><idno type="RBID">pubmed:29880033</idno><idno type="pmid">29880033</idno><idno type="doi">10.1186/s40001-018-0328-7</idno><idno type="wicri:Area/PubMed/Corpus">000876</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000876</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Membrane-bound estrogen receptor alpha initiated signaling is dynamin dependent in breast cancer cells.</title><author><name sortKey="Marczell, Istvan" sort="Marczell, Istvan" uniqKey="Marczell I" first="Istvan" last="Marczell">Istvan Marczell</name><affiliation><nlm:affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Balogh, Petra" sort="Balogh, Petra" uniqKey="Balogh P" first="Petra" last="Balogh">Petra Balogh</name><affiliation><nlm:affiliation>Department of Human Morphology and Developmental Biology, Semmelweis University, Budapest, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Nyiro, Gabor" sort="Nyiro, Gabor" uniqKey="Nyiro G" first="Gabor" last="Nyiro">Gabor Nyiro</name><affiliation><nlm:affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Kiss, Anna L" sort="Kiss, Anna L" uniqKey="Kiss A" first="Anna L" last="Kiss">Anna L. Kiss</name><affiliation><nlm:affiliation>Department of Human Morphology and Developmental Biology, Semmelweis University, Budapest, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Kovacs, Balazs" sort="Kovacs, Balazs" uniqKey="Kovacs B" first="Balazs" last="Kovacs">Balazs Kovacs</name><affiliation><nlm:affiliation>Department of Aquaculture, Szent Istvan University, Godollo, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Bekesi, Gabor" sort="Bekesi, Gabor" uniqKey="Bekesi G" first="Gabor" last="Bekesi">Gabor Bekesi</name><affiliation><nlm:affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Racz, Karoly" sort="Racz, Karoly" uniqKey="Racz K" first="Karoly" last="Racz">Karoly Racz</name><affiliation><nlm:affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</nlm:affiliation></affiliation></author><author><name sortKey="Patocs, Attila" sort="Patocs, Attila" uniqKey="Patocs A" first="Attila" last="Patocs">Attila Patocs</name><affiliation><nlm:affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary. patocs.attila@med.semmelweis-univ.hu.</nlm:affiliation></affiliation></author></analytic><series><title level="j">European journal of medical research</title><idno type="eISSN">2047-783X</idno><imprint><date when="2018" type="published">2018</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Breast Neoplasms (metabolism)</term><term>Cell Membrane (metabolism)</term><term>Dynamins (metabolism)</term><term>Estrogen Receptor alpha (metabolism)</term><term>Female</term><term>Humans</term><term>MCF-7 Cells</term><term>Signal Transduction (physiology)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Dynamins</term><term>Estrogen Receptor alpha</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Breast Neoplasms</term><term>Cell Membrane</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Signal Transduction</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Female</term><term>Humans</term><term>MCF-7 Cells</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Although membrane-associated estrogen receptors (mERs) have been known to play important role in steroid-induced signal transmission, we still know little about their function in the estrogen-induced proliferation of breast cancer cells.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">29880033</PMID><DateCompleted><Year>2018</Year><Month>10</Month><Day>01</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>14</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">2047-783X</ISSN><JournalIssue CitedMedium="Internet"><Volume>23</Volume><Issue>1</Issue><PubDate><Year>2018</Year><Month>Jun</Month><Day>07</Day></PubDate></JournalIssue><Title>European journal of medical research</Title><ISOAbbreviation>Eur. J. Med. Res.</ISOAbbreviation></Journal><ArticleTitle>Membrane-bound estrogen receptor alpha initiated signaling is dynamin dependent in breast cancer cells.</ArticleTitle><Pagination><MedlinePgn>31</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1186/s40001-018-0328-7</ELocationID><Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Although membrane-associated estrogen receptors (mERs) have been known to play important role in steroid-induced signal transmission, we still know little about their function in the estrogen-induced proliferation of breast cancer cells.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">In our current work we tried to separate membrane-initiated estrogen receptor signaling from the overall estrogenic effect in MCF-7 breast carcinoma cells. Re-analyzing expression data from multiple microarray experiments, we selected a set of key regulatory genes involved in proliferation regulation and estrogen signaling to monitor estrogen-induced transcription changes. We then compared these expression changes after 17β-estradiol and a membrane receptor selective estrogen-BSA treatment using quantitative real-time PCR. In order to follow receptor trafficking we used light and electron microscopy.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">Our quantitative real-time PCR results confirmed that the selective membrane receptor agonist, estrogen-BSA induces similarly pronounced expression changes regarding these genes as 17β-estradiol. Morphological study revealed that the membrane-bound form of classical estrogen receptor alpha is internalized after ligand binding via dynamin-dependent, caveola-mediated endocytosis. Inhibition of this internalization with dynamin inhibitor, dynasore practically abolished the regulatory effect of E2-BSA, suggesting that interaction and internalization with the scaffold protein is necessary for effective signaling.</AbstractText><AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The physiological role of plasma membrane estrogen receptor alpha is intensively studied, yet there are still several aspects of it to be resolved. The dynamin-dependent, ligand-mediated internalization of mERs seems to play an important role in estrogen signaling. Our results may serve as another example of how membrane initiated estrogen signaling and nuclear receptor initiated signaling overlap and form an intertwined system.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Marczell</LastName><ForeName>Istvan</ForeName><Initials>I</Initials><Identifier Source="ORCID">http://orcid.org/0000-0003-3982-6187</Identifier><AffiliationInfo><Affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Balogh</LastName><ForeName>Petra</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Department of Human Morphology and Developmental Biology, Semmelweis University, Budapest, Hungary.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Nyiro</LastName><ForeName>Gabor</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Molecular Medicine Research Group, Hungarian Academy of Sciences, Budapest, Szentkirályi str. 46., 1088, Hungary.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kiss</LastName><ForeName>Anna L</ForeName><Initials>AL</Initials><AffiliationInfo><Affiliation>Department of Human Morphology and Developmental Biology, Semmelweis University, Budapest, Hungary.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kovacs</LastName><ForeName>Balazs</ForeName><Initials>B</Initials><AffiliationInfo><Affiliation>Department of Aquaculture, Szent Istvan University, Godollo, Hungary.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Bekesi</LastName><ForeName>Gabor</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Racz</LastName><ForeName>Karoly</ForeName><Initials>K</Initials><AffiliationInfo><Affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Department of Human Morphology and Developmental Biology, Semmelweis University, Budapest, Hungary.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Patocs</LastName><ForeName>Attila</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>2nd Department of Medicine, Semmelweis University, Budapest, Szentkirályi utca 46., 1088, Hungary. patocs.attila@med.semmelweis-univ.hu.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>HAS-SE 'Lendület' Hereditary Endocrine Tumors Research Group, Hungarian Academy of Sciences, Semmelweis University, Budapest, 46. Szentkiralyi str, 1088, Hungary. patocs.attila@med.semmelweis-univ.hu.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Department of Laboratory Medicine, Semmelweis University, Budapest, Nagyvárad sq 4, 1089, Hungary. patocs.attila@med.semmelweis-univ.hu.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>KTIA-AIK-2012-12-1-0010</GrantID><Agency>Technology Innovation Fund, National Developmental Agency</Agency><Country></Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2018</Year><Month>06</Month><Day>07</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Eur J Med Res</MedlineTA><NlmUniqueID>9517857</NlmUniqueID><ISSNLinking>0949-2321</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance 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