Evidence map›Paper›PMID 30649385›Full record

ArticleJournal of the National Cancer Institute2019

The Genomic Landscape of Mucinous Breast Cancer.

Fresia Pareja, Ju Youn Lee, David N Brown, Salvatore Piscuoglio, Rodrigo Gularte-Mérida, Pier Selenica, Arnaud Da Cruz Paula, Sasi Arunachalam, Rahul Kumar, Felipe C Geyer and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

56 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. Characteristics of fusion genes in breast cancer.Cancer cell international · 2026
    Review
  3. Article
  4. Review
  5. The Power of MUC2 in Mucinous Adenocarcinomas.Pathobiology : journal of immunopathology, molecular and cellular biology · 2026
    Review
  6. Molecular and microenvironmental landscapes of human papillomavirus-independent invasive squamous cell carcinoma of the vulva.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2025
    Article
  7. Review
  8. Molecular Basis of Breast Tumor Heterogeneity.Advances in experimental medicine and biology · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Nonlobular Invasive Breast Carcinomas with Biallelic Pathogenic CDH1 Somatic Alterations: A Histologic, Immunophenotypic, and Genomic Characterization.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2024
    Article
  13. Journal of clinical pathology · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

23 authors at 5 institutions in 5 countries.

Fresia ParejaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Ju Youn LeeDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
David N BrownDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Salvatore PiscuoglioDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Rodrigo Gularte-MéridaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Pier SelenicaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Arnaud Da Cruz PaulaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Sasi ArunachalamDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Rahul KumarDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Felipe C GeyerDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Catarina SilveiraDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Edaise M da SilvaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Anqi LiDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Caterina MarchiòDepartment of Medical Sciences, FPO-Canndiolo Cancer Institute, University of Turin, Turin, Italy.
Charlotte K Y NgDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Odette MarianiDépartment de Médecine Diagnostique et Théranostique, Institute Curie, Paris, France.
Laetitia FuhrmannDépartment de Médecine Diagnostique et Théranostique, Institute Curie, Paris, France.
Hannah Y WenDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Larry NortonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Anne Vincent-SalomonDépartment de Médecine Diagnostique et Théranostique, Institute Curie, Paris, France.
Edi BrogiDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Jorge S Reis-FilhoDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Britta WeigeltDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Memorial Sloan Kettering Cancer Center · USInstitut Curie · FRUniversity Hospital of Basel · CHUniversity of Lisbon · PTUniversity of Turin · IT

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Mucinous carcinoma of the breast (MCB) is a rare histologic form of estrogen receptor (ER)-positive/HER2-negative breast cancer (BC) characterized by tumor cells floating in lakes of mucin. We assessed the genomic landscape of 32 MCBs by whole-exome sequencing and/or RNA-sequencing. GATA3 (23.8%), KMT2C (19.0%), and MAP3K1 (14.3%) were the most frequently mutated genes in pure MCBs. In addition, two recurrent but not pathognomonic fusion genes, OAZ1-CSNK1G2 and RFC4-LPP, were detected in 3/31 (9.7%) and 2/31 (6.5%) samples, respectively. Compared with ER-positive/HER2-negative common forms of BC, MCBs displayed lower PIK3CA and TP53 mutation rates and fewer concurrent 1q gains and 16q losses. Clonal decomposition analysis of the mucinous and ductal components independently microdissected from five mixed MCBs revealed that they are clonally related and evolve following clonal selection or parallel evolution. Our findings indicate that MCB represents a genetically distinct ER-positive/HER2-negative form of BC.

Indexed as

Genetic Predisposition to DiseaseAdenocarcinoma, MucinousAgedBiomarkers, TumorBreast NeoplasmsClass I Phosphatidylinositol 3-KinasesClonal EvolutionCytoskeletal ProteinsErb-b2 Receptor Tyrosine KinasesEstrogen Receptor alphaExome SequencingFemaleHumansLIM Domain ProteinsMiddle AgedMucinsBiomarkers, TumorClass I Phosphatidylinositol 3-KinasesCytoskeletal ProteinsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesEstrogen Receptor alphaLIM Domain ProteinsLPP protein, humanMucinsOncogene Proteins, Fusionornithine decarboxylase antizymePIK3CA protein, humanProteinsReplication Protein CRFC4 protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID30649385
PMCPMC6624163
OpenAlexW2909941416

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.