Evidence map›Paper›PMID 18726004›Full record

ArticleInternational journal of biological sciences2008

Aberrant c-erbB2 expression in cell clusters overlying focally disrupted breast myoepithelial cell layers: a trigger or sign for emergence of more aggressive cell clones?

Xichen Zhang, Shahreyar Shar Hashemi, Morvarid Yousefi, Jinsong Ni, Qiuyue Wang, Ling Gao, Pengtao Gong, Chunling Gao, Joy Sheng, Jeffrey Mason and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

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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

11 authors at 5 institutions in 2 countries.

Xichen ZhangCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun, Jilin, China.
Shahreyar Shar Hashemi
Morvarid Yousefi
Jinsong Ni
Qiuyue Wang
Ling Gao
Pengtao Gong
Chunling Gao
Joy Sheng
Jeffrey Mason
Yan-gao Man
Jilin University · CNArmed Forces Institute of Pathology · USStaten Island University Hospital · USFirst Bethune Hospital of Jilin University · CNUnited States Food and Drug Administration · US

Funding

NCI NIH HHS N02 PC051308
6 · The paper itself

Abstract

Our recent studies revealed that cell clusters overlying focal myoepithelial cell layer disruption (FMCLD) had a significantly higher frequency of genetic instabilities and expression of invasion-related genes than their adjacent counterparts within the same duct. Our current study attempted to assess whether these cell clusters would also have elevated c-erbB2 expression. Human breast tumors (n=50) with a high frequency of FMCLD were analyzed with double immunohistochemistry, real-time RT-PCR, and chromogenic in situ hybridization for c-erbB2 protein and gene expression. Of 448 FMCLD detected, 404 (90.2%) were associated with cell clusters that had intense c-erbB2 immunoreactivities primarily in their cytoplasm, in contrast to their adjacent counterparts within the same duct, which had no or barely detectable c-erbB2 expression. These c-erbB2 positive cells were arranged as tongue-like projections, "puncturing" into the stroma, and about 20% of them were in direct continuity with tube-like structures that resembled blood vessels. Aberrant c-erbB2 expression was also seen in clusters of architecturally normal-appearing ducts that had distinct cytological abnormalities in both ME and epithelial cells, whereas not in their clear-cut normal counterparts. Molecular assays detected markedly higher c-erbB2 mRNA and gene amplification in cell clusters associated with FMCLD than in those associated with non-disrupted ME cell layers. Our findings suggest that cell clusters overlying FMCLD may represent the precursors of pending invasive lesions, and that aberrant c-erbB2 expression may trigger or signify the emergence of biologically more aggressive cell clones.

Indexed as

Breast NeoplasmsCarcinoma, Intraductal, NoninfiltratingDisease ProgressionEpithelial CellsErb-b2 Receptor Tyrosine KinasesFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryIn Situ HybridizationNeoplasm InvasivenessReverse Transcriptase Polymerase Chain ReactionErb-b2 Receptor Tyrosine Kinasesc-erbB2monoclonal proliferationmyoepithelial cellsTumor invasiontumor stem cells

Identifiers

PMID18726004
PMCPMC2519838
OpenAlexW2161680084

What OpenQuestion holds

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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.