Evidence map›Paper›PMID 29093438›Full record

ArticleNature communications2017

Mapping genomic and transcriptomic alterations spatially in epithelial cells adjacent to human breast carcinoma.

Moustafa Abdalla, Danh Tran-Thanh, Juan Moreno, Vladimir Iakovlev, Ranju Nair, Nisha Kanwar, Mohamed Abdalla, Jennifer P Y Lee, Jennifer Yin Yee Kwan, Thomas R Cawthorn and 11 more

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Trial
  2. Article
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  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Field cancerization in breast cancer.The Journal of pathology · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. 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

21 authors.

Moustafa AbdallaCampbell Family Institute for Breast Cancer Research, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada, M5G 2M9.
Danh Tran-ThanhDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada, M5S 1A1.
Juan MorenoDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada, M5S 1A1.
Vladimir IakovlevDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada, M5S 1A1.
Ranju NairCampbell Family Institute for Breast Cancer Research, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada, M5G 2M9.
Nisha KanwarCampbell Family Institute for Breast Cancer Research, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada, M5G 2M9.
Mohamed AbdallaDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada, M5S 1A1.
Jennifer P Y LeeDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada, M5S 1A1.
Jennifer Yin Yee KwanDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada, M5S 1A1.
Thomas R CawthornCampbell Family Institute for Breast Cancer Research, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada, M5G 2M9.
Keisha WarrenCampbell Family Institute for Breast Cancer Research, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada, M5G 2M9.
Nona ArnesonCampbell Family Institute for Breast Cancer Research, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada, M5G 2M9.
Dong-Yu WangCampbell Family Institute for Breast Cancer Research, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada, M5G 2M9.ORCID http://orcid.org/0000-0002-5434-287X
Natalie S FoxDepartment of Medical Biophysics, University of Toronto, Toronto, ON, Canada, M5S 1L7.
Bruce J YoungsonDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada, M5S 1A1.
Naomi A MillerDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada, M5S 1A1.
Alexandra M EassonDepartment of Surgical Oncology, Princess Margaret Cancer Center and University of Toronto, Toronto, ON, Canada, M5G 2M9.
David McCreadyDepartment of Surgical Oncology, Princess Margaret Cancer Center and University of Toronto, Toronto, ON, Canada, M5G 2M9.
Wey L LeongDepartment of Surgical Oncology, Princess Margaret Cancer Center and University of Toronto, Toronto, ON, Canada, M5G 2M9.
Paul C BoutrosDepartment of Medical Biophysics, University of Toronto, Toronto, ON, Canada, M5S 1L7.ORCID http://orcid.org/0000-0003-0553-7520
Susan J DoneCampbell Family Institute for Breast Cancer Research, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada, M5G 2M9. sdone@uhnres.utoronto.ca.ORCID http://orcid.org/0000-0002-1770-988X

Funding

CIHR MOP-119469CIHR STP-53912
6 · The paper itself

Abstract

Almost all genomic studies of breast cancer have focused on well-established tumours because it is technically challenging to study the earliest mutational events occurring in human breast epithelial cells. To address this we created a unique dataset of epithelial samples ductoscopically obtained from ducts leading to breast carcinomas and matched samples from ducts on the opposite side of the nipple. Here, we demonstrate that perturbations in mRNA abundance, with increasing proximity to tumour, cannot be explained by copy number aberrations. Rather, we find a possibility of field cancerization surrounding the primary tumour by constructing a classifier that evaluates where epithelial samples were obtained relative to a tumour (cross-validated micro-averaged AUC = 0.74). We implement a spectral co-clustering algorithm to define biclusters. Relating to over-represented bicluster pathways, we further validate two genes with tissue microarrays and in vitro experiments. We highlight evidence suggesting that bicluster perturbation occurs early in tumour development.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastCell Cycle ProteinsComparative Genomic HybridizationEpithelial CellsFemaleGene Expression ProfilingGenome, HumanGenomicsHumansMCF-7 CellsMutationNeoplasm GradingOligonucleotide Array Sequence AnalysisRNA-Binding ProteinsRNA, MessengerCell Cycle ProteinsMSI2 protein, humanRNA-Binding ProteinsRNA, MessengerSPAG5 protein, human

Identifiers

PMID29093438
PMCPMC5665998

What OpenQuestion holds

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LicenceCC BY
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.