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Variances in the Expression of mRNAs and miRNAs Related to the Histaminergic System in Endometrioid Endometrial Cancer
Research has indicated higher concentrations of histamine and polyamine in endometrioid tissue in comparison with healthy tissue. The aim of this study was to evaluate changes in the expression patterns of messenger RNA (mRNAs) and microRNA (miRNAs) related to the histaminergic system in endometrial...
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Published in: | Biomedicines 2021-10, Vol.9 (11), p.1535 |
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description | Research has indicated higher concentrations of histamine and polyamine in endometrioid tissue in comparison with healthy tissue. The aim of this study was to evaluate changes in the expression patterns of messenger RNA (mRNAs) and microRNA (miRNAs) related to the histaminergic system in endometrial samples and whole blood in women with endometrioid endometrial cancer. The study group consisted of 30 women with endometrioid endometrial cancer qualified for hysterectomy (G1 well-differentiated, 15 cases; G2 moderately differentiated, 8 cases; and G3 poorly differentiated, 7 cases). The control group included 30 women with no neoplastic changes during routine gynecological examinations. The molecular analysis consisted of the microarray analysis of mRNAs and miRNAs related to the histaminergic system, reverse-transcription quantitative polymerase chain reaction (RTqPCR), and enzyme-linked immunosorbent assay (ELISA). Out of 65 mRNAs connected with the histaminergic system, 10 differentiate the samples of tissue and blood obtained from patients with endometrioid endometrial cancer in comparison with the control group (p < 0.05). mRNA histamine receptor 1,3 (HRH1, HRH3), and solute carrier family 22 member 3 (SLC23A2) differentiating samples of endometrioid endometrial cancer independent of either G or control. The highest probability of interaction, based on the target score miRDB, between the selected miRNAs and mRNAs was found for the hybrids hsa-miR-1-3p and endothelin 1 (END1), hsa-miR-27a-5β and SLC23A2. The selected mRNA and miRNA transcripts seem to be promising for molecularly targeted therapies in the context of endometrioid endometrial cancer. |
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The aim of this study was to evaluate changes in the expression patterns of messenger RNA (mRNAs) and microRNA (miRNAs) related to the histaminergic system in endometrial samples and whole blood in women with endometrioid endometrial cancer. The study group consisted of 30 women with endometrioid endometrial cancer qualified for hysterectomy (G1 well-differentiated, 15 cases; G2 moderately differentiated, 8 cases; and G3 poorly differentiated, 7 cases). The control group included 30 women with no neoplastic changes during routine gynecological examinations. The molecular analysis consisted of the microarray analysis of mRNAs and miRNAs related to the histaminergic system, reverse-transcription quantitative polymerase chain reaction (RTqPCR), and enzyme-linked immunosorbent assay (ELISA). Out of 65 mRNAs connected with the histaminergic system, 10 differentiate the samples of tissue and blood obtained from patients with endometrioid endometrial cancer in comparison with the control group (p < 0.05). mRNA histamine receptor 1,3 (HRH1, HRH3), and solute carrier family 22 member 3 (SLC23A2) differentiating samples of endometrioid endometrial cancer independent of either G or control. The highest probability of interaction, based on the target score miRDB, between the selected miRNAs and mRNAs was found for the hybrids hsa-miR-1-3p and endothelin 1 (END1), hsa-miR-27a-5β and SLC23A2. The selected mRNA and miRNA transcripts seem to be promising for molecularly targeted therapies in the context of endometrioid endometrial cancer.</description><identifier>ISSN: 2227-9059</identifier><identifier>EISSN: 2227-9059</identifier><identifier>DOI: 10.3390/biomedicines9111535</identifier><identifier>PMID: 34829764</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Cancer ; DNA microarrays ; Endometrial cancer ; endometrioid endometrial cancer ; Endometrium ; Endothelin 1 ; Endothelins ; Enzyme-linked immunosorbent assay ; Gene expression ; grading ; Gynecology ; Histamine ; Histamine receptors ; histaminergic system ; Hormone replacement therapy ; Hybrids ; Hysterectomy ; Manufacturers ; microRNA ; MicroRNAs ; miRNA ; molecular marker ; Obesity ; Obstetrics ; Patients ; Polyamines ; Polymerase chain reaction ; Reagents ; Tumors ; Womens health</subject><ispartof>Biomedicines, 2021-10, Vol.9 (11), p.1535</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-35e5dc872b0605b89a1fc860cae8edb19fb71921fd38f1eefc781a6f2b3f7d93</citedby><cites>FETCH-LOGICAL-c476t-35e5dc872b0605b89a1fc860cae8edb19fb71921fd38f1eefc781a6f2b3f7d93</cites><orcidid>0000-0002-2691-5829 ; 0000-0001-9871-7082 ; 0000-0002-8395-279X ; 0000-0003-1633-7145 ; 0000-0001-8931-3182</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2602016504/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2602016504?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids></links><search><creatorcontrib>Czerwiński, Michał</creatorcontrib><creatorcontrib>Bednarska-Czerwińska, Anna</creatorcontrib><creatorcontrib>Ordon, Paweł</creatorcontrib><creatorcontrib>Gradzik, Magdalena</creatorcontrib><creatorcontrib>Oplawski, Marcin</creatorcontrib><creatorcontrib>Boroń, Dariusz</creatorcontrib><creatorcontrib>Zientek, Hanna</creatorcontrib><creatorcontrib>Ogloszka, Oskar</creatorcontrib><creatorcontrib>Grabarek, Beniamin Oskar</creatorcontrib><title>Variances in the Expression of mRNAs and miRNAs Related to the Histaminergic System in Endometrioid Endometrial Cancer</title><title>Biomedicines</title><description>Research has indicated higher concentrations of histamine and polyamine in endometrioid tissue in comparison with healthy tissue. The aim of this study was to evaluate changes in the expression patterns of messenger RNA (mRNAs) and microRNA (miRNAs) related to the histaminergic system in endometrial samples and whole blood in women with endometrioid endometrial cancer. The study group consisted of 30 women with endometrioid endometrial cancer qualified for hysterectomy (G1 well-differentiated, 15 cases; G2 moderately differentiated, 8 cases; and G3 poorly differentiated, 7 cases). The control group included 30 women with no neoplastic changes during routine gynecological examinations. The molecular analysis consisted of the microarray analysis of mRNAs and miRNAs related to the histaminergic system, reverse-transcription quantitative polymerase chain reaction (RTqPCR), and enzyme-linked immunosorbent assay (ELISA). Out of 65 mRNAs connected with the histaminergic system, 10 differentiate the samples of tissue and blood obtained from patients with endometrioid endometrial cancer in comparison with the control group (p < 0.05). mRNA histamine receptor 1,3 (HRH1, HRH3), and solute carrier family 22 member 3 (SLC23A2) differentiating samples of endometrioid endometrial cancer independent of either G or control. The highest probability of interaction, based on the target score miRDB, between the selected miRNAs and mRNAs was found for the hybrids hsa-miR-1-3p and endothelin 1 (END1), hsa-miR-27a-5β and SLC23A2. The selected mRNA and miRNA transcripts seem to be promising for molecularly targeted therapies in the context of endometrioid endometrial cancer.</description><subject>Cancer</subject><subject>DNA microarrays</subject><subject>Endometrial cancer</subject><subject>endometrioid endometrial cancer</subject><subject>Endometrium</subject><subject>Endothelin 1</subject><subject>Endothelins</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Gene expression</subject><subject>grading</subject><subject>Gynecology</subject><subject>Histamine</subject><subject>Histamine receptors</subject><subject>histaminergic system</subject><subject>Hormone replacement therapy</subject><subject>Hybrids</subject><subject>Hysterectomy</subject><subject>Manufacturers</subject><subject>microRNA</subject><subject>MicroRNAs</subject><subject>miRNA</subject><subject>molecular marker</subject><subject>Obesity</subject><subject>Obstetrics</subject><subject>Patients</subject><subject>Polyamines</subject><subject>Polymerase chain reaction</subject><subject>Reagents</subject><subject>Tumors</subject><subject>Womens health</subject><issn>2227-9059</issn><issn>2227-9059</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt9rFDEQgBdRbKn9C3xZ8MWX0_ze5EUox2kLRaEWX8NsMrnm2N2cSa60_717d0WtmJfMJB_fDMM0zVtKPnBuyMc-phF9dHHCYiilkssXzSljrFsYIs3Lv-KT5ryUDZmPoVxT8bo54UIz0ylx2tz_gBxhcljaOLX1DtvVwzZjKTFNbQrtePP1orQw-XaMh_AGB6jo25oO9GUsFca5i7yOrv3-WCqOe9Nq8nODNccU_Z8Ehna5L5bfNK8CDAXPn-6z5vbz6nZ5ubj-9uVqeXG9cKJTdcElSu90x3qiiOy1ARqcVsQBavQ9NaHvqGE0eK4DRQyu0xRUYD0PnTf8rLk6an2Cjd3mOEJ-tAmiPTykvLaQa3QDWvRaBA0BPBAhjQAlaSc8KEpxX2N2fTq6trt-Hr3DqWYYnkmf_0zxzq7TvdWKSiG6WfD-SZDTzx2WasdYHA4DTJh2xTJFBGGCdXpG3_2DbtIuT_Ok9hQjVEkiZoofKZdTKRnD72Yosfstsf_ZEv4LOkyzfw</recordid><startdate>20211026</startdate><enddate>20211026</enddate><creator>Czerwiński, Michał</creator><creator>Bednarska-Czerwińska, Anna</creator><creator>Ordon, Paweł</creator><creator>Gradzik, Magdalena</creator><creator>Oplawski, Marcin</creator><creator>Boroń, Dariusz</creator><creator>Zientek, Hanna</creator><creator>Ogloszka, Oskar</creator><creator>Grabarek, Beniamin Oskar</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2691-5829</orcidid><orcidid>https://orcid.org/0000-0001-9871-7082</orcidid><orcidid>https://orcid.org/0000-0002-8395-279X</orcidid><orcidid>https://orcid.org/0000-0003-1633-7145</orcidid><orcidid>https://orcid.org/0000-0001-8931-3182</orcidid></search><sort><creationdate>20211026</creationdate><title>Variances in the Expression of mRNAs and miRNAs Related to the Histaminergic System in Endometrioid Endometrial Cancer</title><author>Czerwiński, Michał ; 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The aim of this study was to evaluate changes in the expression patterns of messenger RNA (mRNAs) and microRNA (miRNAs) related to the histaminergic system in endometrial samples and whole blood in women with endometrioid endometrial cancer. The study group consisted of 30 women with endometrioid endometrial cancer qualified for hysterectomy (G1 well-differentiated, 15 cases; G2 moderately differentiated, 8 cases; and G3 poorly differentiated, 7 cases). The control group included 30 women with no neoplastic changes during routine gynecological examinations. The molecular analysis consisted of the microarray analysis of mRNAs and miRNAs related to the histaminergic system, reverse-transcription quantitative polymerase chain reaction (RTqPCR), and enzyme-linked immunosorbent assay (ELISA). Out of 65 mRNAs connected with the histaminergic system, 10 differentiate the samples of tissue and blood obtained from patients with endometrioid endometrial cancer in comparison with the control group (p < 0.05). mRNA histamine receptor 1,3 (HRH1, HRH3), and solute carrier family 22 member 3 (SLC23A2) differentiating samples of endometrioid endometrial cancer independent of either G or control. The highest probability of interaction, based on the target score miRDB, between the selected miRNAs and mRNAs was found for the hybrids hsa-miR-1-3p and endothelin 1 (END1), hsa-miR-27a-5β and SLC23A2. 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subjects | Cancer DNA microarrays Endometrial cancer endometrioid endometrial cancer Endometrium Endothelin 1 Endothelins Enzyme-linked immunosorbent assay Gene expression grading Gynecology Histamine Histamine receptors histaminergic system Hormone replacement therapy Hybrids Hysterectomy Manufacturers microRNA MicroRNAs miRNA molecular marker Obesity Obstetrics Patients Polyamines Polymerase chain reaction Reagents Tumors Womens health |
title | Variances in the Expression of mRNAs and miRNAs Related to the Histaminergic System in Endometrioid Endometrial Cancer |
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