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Patients with Invasive Lobular Carcinoma Show a Significant Increase in IRS-4 Expression Compared to Infiltrative Ductal Carcinoma—A Histopathological Study

dc.contributor.authorOrtega, Miguel A.
dc.contributor.authorFraile Martínez, Oscar
dc.contributor.authorGarcía Montero, Cielo
dc.contributor.authorBorja Vergel, Sandra
dc.contributor.authorTorres Carranza, Diego
dc.contributor.authorPekarek, Leonel
dc.contributor.authorBravo Arribas, Coral
dc.contributor.authorDe León Luis, Juan Antonio
dc.contributor.authorSánchez Rojo, Cristina
dc.contributor.authorÁlvarez Mon, Miguel Ángel
dc.contributor.authorGarcía Honduvilla, Natalio
dc.contributor.authorBujan, Julia
dc.contributor.authorCoca, Santiago
dc.contributor.authorÁlvarez Mon, Melchor
dc.contributor.authorSaez, Miguel A.
dc.contributor.authorGuijarro, Luis G.
dc.date.accessioned2023-06-22T11:08:53Z
dc.date.available2023-06-22T11:08:53Z
dc.date.issued2022-05-28
dc.description.abstractBackground and Objectives: Breast cancer (BC) is the first diagnosed type of cancer and the second leading cause of cancer-related mortality in women. In addition, despite the improvement in treatment and survival in these patients, the global prevalence and incidence of this cancer are rising, and its mortality may be different according to the histological subtype. Invasive lobular carcinoma (ILC) is less common but entails a poorer prognosis than infiltrative ductal carcinoma (IDC), exhibiting a different clinical and histopathological profile. Deepening study on the molecular profile of both types of cancer may be of great aid to understand the carcinogenesis and progression of BC. In this sense, the aim of the present study was to explore the histological expression of Insulin receptor substrate 4 (IRS-4), cyclooxygenase 2 (COX-2), Cyclin D1 and retinoblastoma protein 1 (Rb1) in patients with ILC and IDC. Patients and Methods: Thus, breast tissue samples from 45 patients with ILC and from 45 subjects with IDC were analyzed in our study. Results: Interestingly, we observed that IRS-4, COX-2, Rb1 and Cyclin D1 were overexpressed in patients with ILC in comparison to IDC. Conclusions: These results may indicate a differential molecular profile between both types of tumors, which may explain the clinical differences among ILC and IDC. Further studies are warranted in order to shed light onto the molecular and translational implications of these components, also aiding to develop a possible targeted therapy to improve the clinical management of these patients.
dc.description.departmentDepto. de Salud Pública y Materno - Infantil
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.sponsorshipComunidad de Madrid
dc.description.sponsorshipHALEKULANI, S.L.
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/78028
dc.identifier.doi10.3390/medicina58060722
dc.identifier.issn1648-9144
dc.identifier.officialurlhttps://doi.org/10.3390/medicina58060722
dc.identifier.relatedurlhttps://www.mdpi.com/1648-9144/58/6/722
dc.identifier.urihttps://hdl.handle.net/20.500.14352/72151
dc.issue.number6
dc.journal.titleMedicina
dc.language.isoeng
dc.page.initial722
dc.publisherMDPI
dc.relation.projectIDB2017/BMD-3804 MITIC-CM, B2020/MITICAD-CM
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu616-006.04
dc.subject.cdu611.018
dc.subject.keywordBreast cancer (BC)
dc.subject.keywordInvasive lobular carcinoma (ILC)
dc.subject.keywordInsulin receptor substrate 4 (IRS-4)
dc.subject.keywordCyclooxygenase 2 (COX-2)
dc.subject.keywordCyclin D1
dc.subject.keywordRetinoblastoma protein 1 (Rb1)
dc.subject.ucmMedicina
dc.subject.ucmHistología
dc.subject.ucmOncología
dc.subject.unesco32 Ciencias Médicas
dc.subject.unesco2410.08 Histología Humana
dc.subject.unesco3201.01 Oncología
dc.titlePatients with Invasive Lobular Carcinoma Show a Significant Increase in IRS-4 Expression Compared to Infiltrative Ductal Carcinoma—A Histopathological Study
dc.typejournal article
dc.volume.number58
dspace.entity.typePublication
relation.isAuthorOfPublicatione2778567-7775-46c0-b81b-1f4f22c18a6c
relation.isAuthorOfPublication.latestForDiscoverye2778567-7775-46c0-b81b-1f4f22c18a6c

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