Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis
- Autores
- Lleyda, Micaela; Mendez Brito, Sandra; Bernacchia, Juliana Lourdes; Costas, Monica Alejandra; Vazquez Levin, Mónica H.
- Año de publicación
- 2022
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- Colorectal cancer (CRC) is the most common malignant diseaseof the digestive tract, and 2nd in incidence/mortality worldwide andin Argentina. Epithelial Cadherin (Ecad) loss has been related tocell adhesion loss, migration and invasiveness. FXYD5/Dysadherin(FXYD5) was found associated with tumor aggressiveness/metastasis in solid tumors and is a negative Ecad modulator. Studieswere initiated to characterize Ecad and FXYD5 expression inCRC and their role in tumor progression/metastasis. Transcriptexpression analysis was done in datasets from colon adenomaand CRC patient’s and cell lines (GEO; TCGA). Paired adenomas/normal tissue analysis (GSE8671; n=32) revealed decreasedECad (NT=20,884±3,342; A=16,855±2,082) and increased FXYD5(NT=1,107±435; A=3,577±1,193) (p<0.0001) in adenomas. In linewith these findings, lower Ecad and higher FXYD5 was foundin early tumors when comparing to normal tissues (GSE32323;16 pairs, Ecad NT=13.21±0.19 T=12.86±0.32, p<0.005; FXYD5NT=7.65±0.47 T=8.72±0.43, p<0.005). Similar results were obtainedin other CRC datasets (GSE4107; NT n=10 T n=12; Ecadp<0.05, FXYD5 p<0.05; GSE9348; NT n=12 T n=70; Ecad p<0.05,FXYD5 p<0.001). No differences in Ecad and FXYD5 expressionwere observed with patient gender (female n=30, male n=40; Ecadp=0.9448, FXYD5 p=0.6735) or age (50-69y (n=43), 70-93y (n=27)Ecad=0.1482; FXYD5=0.3671). When comparing MSS (n=13) andMSI (n=77) tumors (GSE24550), MSI showed higher (p<0.0001)FXYD5 and similar (p=0.1084 Ecad levels). Overall survival (TCGA)was lower (p=0.0064) in patients with high (5.153 y; n=246) thanlow (8.334 y; n=351) FXYD5. Moreover, liver metastasis (n=283;GSE159216) also showed higher FXYD5 levels (p<0.0001) thantumors (n=105; GSE178120), while Ecad levels were comparable(p=0.24). Ecad and FXYD5 expression was confirmed in HT29(High Ecad, Low FXYD5) and HCT116 (Low Ecad, High FXYD5)and are currently under study to assess the underlying mechanismsof CRC progression/aggressiveness.
Fil: Lleyda, Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina
Fil: Mendez Brito, Sandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina
Fil: Bernacchia, Juliana Lourdes. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Costas, Monica Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina
Fil: Vazquez Levin, Mónica H.. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina
LXVII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXX Reunión Anual de la Sociedad Argentina de Inmunología; 3er Congreso Franco Argentino de Inmunología y Reunión Anual 2022 de la Sociedad Argentina de Fisiología
Argentina
Sociedad Argentina de Investigación Clínica
Sociedad Argentina de Inmunología
Sociedad Argentina de Fisiología - Materia
-
Colorectal cancer
FXYD5
E-CADHERIN - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/242530
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Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasisLleyda, MicaelaMendez Brito, SandraBernacchia, Juliana LourdesCostas, Monica AlejandraVazquez Levin, Mónica H.Colorectal cancerFXYD5E-CADHERINhttps://purl.org/becyt/ford/3.5https://purl.org/becyt/ford/3Colorectal cancer (CRC) is the most common malignant diseaseof the digestive tract, and 2nd in incidence/mortality worldwide andin Argentina. Epithelial Cadherin (Ecad) loss has been related tocell adhesion loss, migration and invasiveness. FXYD5/Dysadherin(FXYD5) was found associated with tumor aggressiveness/metastasis in solid tumors and is a negative Ecad modulator. Studieswere initiated to characterize Ecad and FXYD5 expression inCRC and their role in tumor progression/metastasis. Transcriptexpression analysis was done in datasets from colon adenomaand CRC patient’s and cell lines (GEO; TCGA). Paired adenomas/normal tissue analysis (GSE8671; n=32) revealed decreasedECad (NT=20,884±3,342; A=16,855±2,082) and increased FXYD5(NT=1,107±435; A=3,577±1,193) (p<0.0001) in adenomas. In linewith these findings, lower Ecad and higher FXYD5 was foundin early tumors when comparing to normal tissues (GSE32323;16 pairs, Ecad NT=13.21±0.19 T=12.86±0.32, p<0.005; FXYD5NT=7.65±0.47 T=8.72±0.43, p<0.005). Similar results were obtainedin other CRC datasets (GSE4107; NT n=10 T n=12; Ecadp<0.05, FXYD5 p<0.05; GSE9348; NT n=12 T n=70; Ecad p<0.05,FXYD5 p<0.001). No differences in Ecad and FXYD5 expressionwere observed with patient gender (female n=30, male n=40; Ecadp=0.9448, FXYD5 p=0.6735) or age (50-69y (n=43), 70-93y (n=27)Ecad=0.1482; FXYD5=0.3671). When comparing MSS (n=13) andMSI (n=77) tumors (GSE24550), MSI showed higher (p<0.0001)FXYD5 and similar (p=0.1084 Ecad levels). Overall survival (TCGA)was lower (p=0.0064) in patients with high (5.153 y; n=246) thanlow (8.334 y; n=351) FXYD5. Moreover, liver metastasis (n=283;GSE159216) also showed higher FXYD5 levels (p<0.0001) thantumors (n=105; GSE178120), while Ecad levels were comparable(p=0.24). Ecad and FXYD5 expression was confirmed in HT29(High Ecad, Low FXYD5) and HCT116 (Low Ecad, High FXYD5)and are currently under study to assess the underlying mechanismsof CRC progression/aggressiveness.Fil: Lleyda, Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Mendez Brito, Sandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Bernacchia, Juliana Lourdes. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Costas, Monica Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Vazquez Levin, Mónica H.. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaLXVII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXX Reunión Anual de la Sociedad Argentina de Inmunología; 3er Congreso Franco Argentino de Inmunología y Reunión Anual 2022 de la Sociedad Argentina de FisiologíaArgentinaSociedad Argentina de Investigación ClínicaSociedad Argentina de InmunologíaSociedad Argentina de FisiologíaFundación Revista Medicina2022info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/242530Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis; LXVII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXX Reunión Anual de la Sociedad Argentina de Inmunología; 3er Congreso Franco Argentino de Inmunología y Reunión Anual 2022 de la Sociedad Argentina de Fisiología; Argentina; 2022; 1-2CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.medicinabuenosaires.com/PMID/36368022.pdfNacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:35:53Zoai:ri.conicet.gov.ar:11336/242530instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 09:35:54.025CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis |
title |
Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis |
spellingShingle |
Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis Lleyda, Micaela Colorectal cancer FXYD5 E-CADHERIN |
title_short |
Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis |
title_full |
Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis |
title_fullStr |
Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis |
title_full_unstemmed |
Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis |
title_sort |
Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis |
dc.creator.none.fl_str_mv |
Lleyda, Micaela Mendez Brito, Sandra Bernacchia, Juliana Lourdes Costas, Monica Alejandra Vazquez Levin, Mónica H. |
author |
Lleyda, Micaela |
author_facet |
Lleyda, Micaela Mendez Brito, Sandra Bernacchia, Juliana Lourdes Costas, Monica Alejandra Vazquez Levin, Mónica H. |
author_role |
author |
author2 |
Mendez Brito, Sandra Bernacchia, Juliana Lourdes Costas, Monica Alejandra Vazquez Levin, Mónica H. |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Colorectal cancer FXYD5 E-CADHERIN |
topic |
Colorectal cancer FXYD5 E-CADHERIN |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.5 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Colorectal cancer (CRC) is the most common malignant diseaseof the digestive tract, and 2nd in incidence/mortality worldwide andin Argentina. Epithelial Cadherin (Ecad) loss has been related tocell adhesion loss, migration and invasiveness. FXYD5/Dysadherin(FXYD5) was found associated with tumor aggressiveness/metastasis in solid tumors and is a negative Ecad modulator. Studieswere initiated to characterize Ecad and FXYD5 expression inCRC and their role in tumor progression/metastasis. Transcriptexpression analysis was done in datasets from colon adenomaand CRC patient’s and cell lines (GEO; TCGA). Paired adenomas/normal tissue analysis (GSE8671; n=32) revealed decreasedECad (NT=20,884±3,342; A=16,855±2,082) and increased FXYD5(NT=1,107±435; A=3,577±1,193) (p<0.0001) in adenomas. In linewith these findings, lower Ecad and higher FXYD5 was foundin early tumors when comparing to normal tissues (GSE32323;16 pairs, Ecad NT=13.21±0.19 T=12.86±0.32, p<0.005; FXYD5NT=7.65±0.47 T=8.72±0.43, p<0.005). Similar results were obtainedin other CRC datasets (GSE4107; NT n=10 T n=12; Ecadp<0.05, FXYD5 p<0.05; GSE9348; NT n=12 T n=70; Ecad p<0.05,FXYD5 p<0.001). No differences in Ecad and FXYD5 expressionwere observed with patient gender (female n=30, male n=40; Ecadp=0.9448, FXYD5 p=0.6735) or age (50-69y (n=43), 70-93y (n=27)Ecad=0.1482; FXYD5=0.3671). When comparing MSS (n=13) andMSI (n=77) tumors (GSE24550), MSI showed higher (p<0.0001)FXYD5 and similar (p=0.1084 Ecad levels). Overall survival (TCGA)was lower (p=0.0064) in patients with high (5.153 y; n=246) thanlow (8.334 y; n=351) FXYD5. Moreover, liver metastasis (n=283;GSE159216) also showed higher FXYD5 levels (p<0.0001) thantumors (n=105; GSE178120), while Ecad levels were comparable(p=0.24). Ecad and FXYD5 expression was confirmed in HT29(High Ecad, Low FXYD5) and HCT116 (Low Ecad, High FXYD5)and are currently under study to assess the underlying mechanismsof CRC progression/aggressiveness. Fil: Lleyda, Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina Fil: Mendez Brito, Sandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina Fil: Bernacchia, Juliana Lourdes. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Costas, Monica Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentina Fil: Vazquez Levin, Mónica H.. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina LXVII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXX Reunión Anual de la Sociedad Argentina de Inmunología; 3er Congreso Franco Argentino de Inmunología y Reunión Anual 2022 de la Sociedad Argentina de Fisiología Argentina Sociedad Argentina de Investigación Clínica Sociedad Argentina de Inmunología Sociedad Argentina de Fisiología |
description |
Colorectal cancer (CRC) is the most common malignant diseaseof the digestive tract, and 2nd in incidence/mortality worldwide andin Argentina. Epithelial Cadherin (Ecad) loss has been related tocell adhesion loss, migration and invasiveness. FXYD5/Dysadherin(FXYD5) was found associated with tumor aggressiveness/metastasis in solid tumors and is a negative Ecad modulator. Studieswere initiated to characterize Ecad and FXYD5 expression inCRC and their role in tumor progression/metastasis. Transcriptexpression analysis was done in datasets from colon adenomaand CRC patient’s and cell lines (GEO; TCGA). Paired adenomas/normal tissue analysis (GSE8671; n=32) revealed decreasedECad (NT=20,884±3,342; A=16,855±2,082) and increased FXYD5(NT=1,107±435; A=3,577±1,193) (p<0.0001) in adenomas. In linewith these findings, lower Ecad and higher FXYD5 was foundin early tumors when comparing to normal tissues (GSE32323;16 pairs, Ecad NT=13.21±0.19 T=12.86±0.32, p<0.005; FXYD5NT=7.65±0.47 T=8.72±0.43, p<0.005). Similar results were obtainedin other CRC datasets (GSE4107; NT n=10 T n=12; Ecadp<0.05, FXYD5 p<0.05; GSE9348; NT n=12 T n=70; Ecad p<0.05,FXYD5 p<0.001). No differences in Ecad and FXYD5 expressionwere observed with patient gender (female n=30, male n=40; Ecadp=0.9448, FXYD5 p=0.6735) or age (50-69y (n=43), 70-93y (n=27)Ecad=0.1482; FXYD5=0.3671). When comparing MSS (n=13) andMSI (n=77) tumors (GSE24550), MSI showed higher (p<0.0001)FXYD5 and similar (p=0.1084 Ecad levels). Overall survival (TCGA)was lower (p=0.0064) in patients with high (5.153 y; n=246) thanlow (8.334 y; n=351) FXYD5. Moreover, liver metastasis (n=283;GSE159216) also showed higher FXYD5 levels (p<0.0001) thantumors (n=105; GSE178120), while Ecad levels were comparable(p=0.24). Ecad and FXYD5 expression was confirmed in HT29(High Ecad, Low FXYD5) and HCT116 (Low Ecad, High FXYD5)and are currently under study to assess the underlying mechanismsof CRC progression/aggressiveness. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/conferenceObject Reunión Journal http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
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conferenceObject |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/242530 Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis; LXVII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXX Reunión Anual de la Sociedad Argentina de Inmunología; 3er Congreso Franco Argentino de Inmunología y Reunión Anual 2022 de la Sociedad Argentina de Fisiología; Argentina; 2022; 1-2 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/242530 |
identifier_str_mv |
Alterations in epithelial cadherin and fxyd5/dysadherin expression in colorectal cancer progression and metastasis; LXVII Reunión Anual de la Sociedad Argentina de Investigación Clínica; LXX Reunión Anual de la Sociedad Argentina de Inmunología; 3er Congreso Franco Argentino de Inmunología y Reunión Anual 2022 de la Sociedad Argentina de Fisiología; Argentina; 2022; 1-2 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.medicinabuenosaires.com/PMID/36368022.pdf |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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Nacional |
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Fundación Revista Medicina |
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Fundación Revista Medicina |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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