Publication:
The Clonal Relationship Between the Ductal and Lobular Components of Mixed Ductal-Lobular Carcinomas Suggested a Ductal Origin in Most Tumors.

dc.contributor.authorPérez-Mies, Belén
dc.contributor.authorCaniego-Casas, Tamara
dc.contributor.authorCarretero-Barrio, Irene
dc.contributor.authorBiscuola, Michele
dc.contributor.authorLópez-García, María A
dc.contributor.authorHardisson, David
dc.contributor.authorRosas, Marta
dc.contributor.authorLópez Rodríguez, María J
dc.contributor.authorCristóbal, Eva
dc.contributor.authorPizarro, David
dc.contributor.authorRosa-Rosa, Juan M
dc.contributor.authorPalacios, José
dc.date.accessioned2023-05-03T13:28:04Z
dc.date.available2023-05-03T13:28:04Z
dc.date.issued2022-07-25
dc.description.abstractThe relationship between the ductal and lobular components of invasive ductolobular carcinomas (IDLC) has not been fully elucidated. In this study, the molecular alterations of both components were analyzed in a series of 20 IDLC that were selected, not only by morphologic criteria, but also by the loss of E-cadherin expression in the lobular component. We found that 80% of tumors shared alterations of driver genes in both components, being PIK3CA the most common alteration. In addition, 45% of IDLC carried CDH1 mutations in their lobular component that were absent in the ductal component. Fluorescent in situ hybridization analysis of the CDH1 gene excluded homozygous CDH1 loss as a frequent cause of E-cadherin loss in tumors without CDH1 mutations. In addition, no pathogenic mutations of catenin genes were detected in this series of tumors. In 25% of tumors, actionable mutations in PIK3CA , AKT1 , and ERBB2 were found in only 1 component. Altogether, our results confirm that most IDLC derive from invasive carcinoma of no special type, in which a population of cells lose E-cadherin and acquire a lobular phenotype. The frequency of CDH1 mutations in IDLC appears to be lower than in conventional invasive lobular carcinomas, suggesting the implication of alternative mechanisms of E-cadherin loss. Moreover, molecular heterogeneity between ductal and lobular areas suggests the need for molecular characterization of both components to guide targeted therapies.
dc.identifier.doi10.1097/PAS.0000000000001936
dc.identifier.essn1532-0979
dc.identifier.pmcPMC9561241
dc.identifier.pmid35877198
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9561241/pdf
dc.identifier.unpaywallURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9561241
dc.identifier.urihttp://hdl.handle.net/10668/19859
dc.issue.number11
dc.journal.titleThe American journal of surgical pathology
dc.journal.titleabbreviationAm J Surg Pathol
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number1545-1553
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subject.meshBreast Neoplasms
dc.subject.meshCadherins
dc.subject.meshCarcinoma, Ductal, Breast
dc.subject.meshCarcinoma, Intraductal, Noninfiltrating
dc.subject.meshCarcinoma, Lobular
dc.subject.meshCatenins
dc.subject.meshClass I Phosphatidylinositol 3-Kinases
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshIn Situ Hybridization, Fluorescence
dc.titleThe Clonal Relationship Between the Ductal and Lobular Components of Mixed Ductal-Lobular Carcinomas Suggested a Ductal Origin in Most Tumors.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number46
dspace.entity.typePublication

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