Evidence map›Paper›PMID 35877198›Full record

ArticleThe American journal of surgical pathology2022

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

Belén Pérez-Mies, Tamara Caniego-Casas, Irene Carretero-Barrio, Michele Biscuola, María A López-García, David Hardisson, Marta Rosas, María J López Rodríguez, Eva Cristóbal, David Pizarro and 2 more

Abstract read
In one paragraph

Article in The American journal of surgical pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Belén Pérez-MiesDepartment of Pathology, Hospital Ramón y Cajal.
Tamara Caniego-CasasDepartment of Pathology, Hospital Ramón y Cajal.
Irene Carretero-BarrioDepartment of Pathology, Hospital Ramón y Cajal.
Michele BiscuolaCIBERONC.
María A López-GarcíaCIBERONC.
David HardissonCIBERONC.
Marta RosasDepartment of Pathology, Hospital Ramón y Cajal.
María J López RodríguezInstituto Ramon y Cajal de Investigación Sanitaria (IRyCIS).
Eva CristóbalDepartment of Pathology, Hospital Ramón y Cajal.
David PizarroDepartment of Pathology, Hospital Ramón y Cajal.
Juan M Rosa-RosaDepartment of Pathology, Hospital Ramón y Cajal.
José PalaciosDepartment of Pathology, Hospital Ramón y Cajal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 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.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, Intraductal, NoninfiltratingCarcinoma, LobularCadherinsCateninsClass I Phosphatidylinositol 3-KinasesFemaleHumansIn Situ Hybridization, FluorescenceCadherinsCateninsClass I Phosphatidylinositol 3-Kinases

Identifiers

PMID35877198
PMCPMC9561241

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.