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Circulating Endometrial Cells: A New Source of Information on Endometriosis Dynamics
The focus of the presented work was to isolate and characterize circulating endometrial cells (CECs) enriched from peripheral blood (PB) of patients with diagnosed endometriosis. The molecular characteristics of CECs could be supportive for an understanding of endometriosis pathogenesis and treatmen...
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Published in: | Journal of clinical medicine 2019-11, Vol.8 (11), p.1938 |
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container_issue | 11 |
container_start_page | 1938 |
container_title | Journal of clinical medicine |
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creator | Pospisilova, Eliska Kiss, Imrich Souckova, Helena Tomes, Pavel Spicka, Jan Matkowski, Rafal Jedryka, Marcin Ferrero, Simone Bobek, Vladimir Kolostova, Katarina |
description | The focus of the presented work was to isolate and characterize circulating endometrial cells (CECs) enriched from peripheral blood (PB) of patients with diagnosed endometriosis. The molecular characteristics of CECs could be supportive for an understanding of endometriosis pathogenesis and treatment decisions in the future.
Blood samples (
= 423) were tested for CECs presence. Subsequently, gene expression analysis (GEA) was carried out for CECs. In parallel, CECs presence and characteristics were tested during menstrual cycle (MC) phases in 11 patients. CECs were enriched by size-based separation.
CECs were present in 78.4% of the tested blood samples. In line with the revised American Fertility Society (rAFS) classification, CECs presence was confirmed in all the acknowledged endometriosis stages: minimal, mild, moderate, and severe. Surprisingly, CECs negativity rate was also reported for severe disease in 21.1% of cases. The CECs captured during MC phases displayed different cytomorphology, including epithelial, stromal, and stem cell-like characteristics. The highest CECs numbers were detected in the mid-secretory phase of MC, which corresponds to uterine lining decidualization. CECs captured during mid-secretory periods expressed genes
,
, and
in higher amounts when compared to the proliferative phase of MC, where genes
and
were mostly elevated. GEA of the super-positive CECs samples (1000 CECs/8 mL PB) revealed high expression of genes
,
,
, and
. The expression of these genes was also elevated in the endometriosis tissue samples and endometrioma.
The panel of the identified CEC genes could be tested in a prospective manner to confirm the role of CECs in endometriosis pathogenesis and diagnostics. |
doi_str_mv | 10.3390/jcm8111938 |
format | article |
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Blood samples (
= 423) were tested for CECs presence. Subsequently, gene expression analysis (GEA) was carried out for CECs. In parallel, CECs presence and characteristics were tested during menstrual cycle (MC) phases in 11 patients. CECs were enriched by size-based separation.
CECs were present in 78.4% of the tested blood samples. In line with the revised American Fertility Society (rAFS) classification, CECs presence was confirmed in all the acknowledged endometriosis stages: minimal, mild, moderate, and severe. Surprisingly, CECs negativity rate was also reported for severe disease in 21.1% of cases. The CECs captured during MC phases displayed different cytomorphology, including epithelial, stromal, and stem cell-like characteristics. The highest CECs numbers were detected in the mid-secretory phase of MC, which corresponds to uterine lining decidualization. CECs captured during mid-secretory periods expressed genes
,
, and
in higher amounts when compared to the proliferative phase of MC, where genes
and
were mostly elevated. GEA of the super-positive CECs samples (1000 CECs/8 mL PB) revealed high expression of genes
,
,
, and
. The expression of these genes was also elevated in the endometriosis tissue samples and endometrioma.
The panel of the identified CEC genes could be tested in a prospective manner to confirm the role of CECs in endometriosis pathogenesis and diagnostics.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm8111938</identifier><identifier>PMID: 31717910</identifier><language>eng</language><publisher>Switzerland: MDPI</publisher><ispartof>Journal of clinical medicine, 2019-11, Vol.8 (11), p.1938</ispartof><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c378t-bf5ee8db9c97020256b2e16b0875ab84519edf0ba265a202e917dbe1dc08ca983</citedby><cites>FETCH-LOGICAL-c378t-bf5ee8db9c97020256b2e16b0875ab84519edf0ba265a202e917dbe1dc08ca983</cites><orcidid>0000-0003-2225-5568 ; 0000-0002-1705-5097</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912292/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912292/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31717910$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pospisilova, Eliska</creatorcontrib><creatorcontrib>Kiss, Imrich</creatorcontrib><creatorcontrib>Souckova, Helena</creatorcontrib><creatorcontrib>Tomes, Pavel</creatorcontrib><creatorcontrib>Spicka, Jan</creatorcontrib><creatorcontrib>Matkowski, Rafal</creatorcontrib><creatorcontrib>Jedryka, Marcin</creatorcontrib><creatorcontrib>Ferrero, Simone</creatorcontrib><creatorcontrib>Bobek, Vladimir</creatorcontrib><creatorcontrib>Kolostova, Katarina</creatorcontrib><title>Circulating Endometrial Cells: A New Source of Information on Endometriosis Dynamics</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>The focus of the presented work was to isolate and characterize circulating endometrial cells (CECs) enriched from peripheral blood (PB) of patients with diagnosed endometriosis. The molecular characteristics of CECs could be supportive for an understanding of endometriosis pathogenesis and treatment decisions in the future.
Blood samples (
= 423) were tested for CECs presence. Subsequently, gene expression analysis (GEA) was carried out for CECs. In parallel, CECs presence and characteristics were tested during menstrual cycle (MC) phases in 11 patients. CECs were enriched by size-based separation.
CECs were present in 78.4% of the tested blood samples. In line with the revised American Fertility Society (rAFS) classification, CECs presence was confirmed in all the acknowledged endometriosis stages: minimal, mild, moderate, and severe. Surprisingly, CECs negativity rate was also reported for severe disease in 21.1% of cases. The CECs captured during MC phases displayed different cytomorphology, including epithelial, stromal, and stem cell-like characteristics. The highest CECs numbers were detected in the mid-secretory phase of MC, which corresponds to uterine lining decidualization. CECs captured during mid-secretory periods expressed genes
,
, and
in higher amounts when compared to the proliferative phase of MC, where genes
and
were mostly elevated. GEA of the super-positive CECs samples (1000 CECs/8 mL PB) revealed high expression of genes
,
,
, and
. The expression of these genes was also elevated in the endometriosis tissue samples and endometrioma.
The panel of the identified CEC genes could be tested in a prospective manner to confirm the role of CECs in endometriosis pathogenesis and diagnostics.</description><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpVkd9LwzAQx4Mobsy9-AdIHkWo5kfbJD4IUqcOhj44n0OapjOjbWbSKvvv7dic8wjcwX3ue5c7AM4xuqZUoJulrjnGWFB-BIYEMRYhyunxQTwA4xCWqDfOY4LZKRhQzDATGA3BPLNed5VqbbOAk6ZwtWm9VRXMTFWFW3gPX8w3fHOd1wa6Ek6b0vm6x10D-7evcMEG-LBuVG11OAMnpaqCGe_8CLw_TubZczR7fZpm97NIU8bbKC8TY3iRCy0YIogkaU4MTnPEWaJyHidYmKJEuSJpovq8EZgVucGFRlwrwekI3G11V11em0KbpvWqkitva-XX0ikr_2ca-yEX7kumAhMiSC9wuRPw7rMzoZW1Dbr_uWqM64IkFMckFkm8Qa-2qPYuBG_KfRuM5OYS8u8SPXxxONge_d07_QHk0YUN</recordid><startdate>20191111</startdate><enddate>20191111</enddate><creator>Pospisilova, Eliska</creator><creator>Kiss, Imrich</creator><creator>Souckova, Helena</creator><creator>Tomes, Pavel</creator><creator>Spicka, Jan</creator><creator>Matkowski, Rafal</creator><creator>Jedryka, Marcin</creator><creator>Ferrero, Simone</creator><creator>Bobek, Vladimir</creator><creator>Kolostova, Katarina</creator><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2225-5568</orcidid><orcidid>https://orcid.org/0000-0002-1705-5097</orcidid></search><sort><creationdate>20191111</creationdate><title>Circulating Endometrial Cells: A New Source of Information on Endometriosis Dynamics</title><author>Pospisilova, Eliska ; Kiss, Imrich ; Souckova, Helena ; Tomes, Pavel ; Spicka, Jan ; Matkowski, Rafal ; Jedryka, Marcin ; Ferrero, Simone ; Bobek, Vladimir ; Kolostova, Katarina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c378t-bf5ee8db9c97020256b2e16b0875ab84519edf0ba265a202e917dbe1dc08ca983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pospisilova, Eliska</creatorcontrib><creatorcontrib>Kiss, Imrich</creatorcontrib><creatorcontrib>Souckova, Helena</creatorcontrib><creatorcontrib>Tomes, Pavel</creatorcontrib><creatorcontrib>Spicka, Jan</creatorcontrib><creatorcontrib>Matkowski, Rafal</creatorcontrib><creatorcontrib>Jedryka, Marcin</creatorcontrib><creatorcontrib>Ferrero, Simone</creatorcontrib><creatorcontrib>Bobek, Vladimir</creatorcontrib><creatorcontrib>Kolostova, Katarina</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pospisilova, Eliska</au><au>Kiss, Imrich</au><au>Souckova, Helena</au><au>Tomes, Pavel</au><au>Spicka, Jan</au><au>Matkowski, Rafal</au><au>Jedryka, Marcin</au><au>Ferrero, Simone</au><au>Bobek, Vladimir</au><au>Kolostova, Katarina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Circulating Endometrial Cells: A New Source of Information on Endometriosis Dynamics</atitle><jtitle>Journal of clinical medicine</jtitle><addtitle>J Clin Med</addtitle><date>2019-11-11</date><risdate>2019</risdate><volume>8</volume><issue>11</issue><spage>1938</spage><pages>1938-</pages><issn>2077-0383</issn><eissn>2077-0383</eissn><abstract>The focus of the presented work was to isolate and characterize circulating endometrial cells (CECs) enriched from peripheral blood (PB) of patients with diagnosed endometriosis. The molecular characteristics of CECs could be supportive for an understanding of endometriosis pathogenesis and treatment decisions in the future.
Blood samples (
= 423) were tested for CECs presence. Subsequently, gene expression analysis (GEA) was carried out for CECs. In parallel, CECs presence and characteristics were tested during menstrual cycle (MC) phases in 11 patients. CECs were enriched by size-based separation.
CECs were present in 78.4% of the tested blood samples. In line with the revised American Fertility Society (rAFS) classification, CECs presence was confirmed in all the acknowledged endometriosis stages: minimal, mild, moderate, and severe. Surprisingly, CECs negativity rate was also reported for severe disease in 21.1% of cases. The CECs captured during MC phases displayed different cytomorphology, including epithelial, stromal, and stem cell-like characteristics. The highest CECs numbers were detected in the mid-secretory phase of MC, which corresponds to uterine lining decidualization. CECs captured during mid-secretory periods expressed genes
,
, and
in higher amounts when compared to the proliferative phase of MC, where genes
and
were mostly elevated. GEA of the super-positive CECs samples (1000 CECs/8 mL PB) revealed high expression of genes
,
,
, and
. The expression of these genes was also elevated in the endometriosis tissue samples and endometrioma.
The panel of the identified CEC genes could be tested in a prospective manner to confirm the role of CECs in endometriosis pathogenesis and diagnostics.</abstract><cop>Switzerland</cop><pub>MDPI</pub><pmid>31717910</pmid><doi>10.3390/jcm8111938</doi><orcidid>https://orcid.org/0000-0003-2225-5568</orcidid><orcidid>https://orcid.org/0000-0002-1705-5097</orcidid><oa>free_for_read</oa></addata></record> |
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title | Circulating Endometrial Cells: A New Source of Information on Endometriosis Dynamics |
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