Evidence map›Paper›PMID 27240462›Full record

ArticleVirchows Archiv : an international journal of pathology2016

The unique luminal staining pattern of cytokeratin 5/6 in adenoid cystic carcinoma of the breast may aid in differentiating it from its mimickers.

Tokiko Nakai, Shu Ichihara, Akiko Kada, Noriko Ito, Suzuko Moritani, Tomonori Kawasaki, Tomoko Uchiyama, Hiroe Itami, Kouhei Morita, Masato Takano and 3 more

Abstract read
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Article in Virchows Archiv : an international journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

3 citing papers in PubMed, 15 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

13 authors at 4 institutions in 1 country.

Tokiko NakaiDepartment of Pathology, Nara Medical University, Kashihara, Nara, Japan.
Shu IchiharaDepartment of Pathology, Clinical Research Center, Nagoya Medical Center, 4-1-1 Sannomaru, Naka-ku, Nagoya, Aichi, Japan. patho@nnh.hosp.go.jp.
Akiko KadaDepartment of Clinical Trials and Research, Clinical Research Center, Nagoya Medical Center, Nagoya, Aichi, Japan.
Noriko ItoDepartment of Clinical Research Management, Clinical Research Center, Nagoya Medical Center, Nagoya, Aichi, Japan.
Suzuko MoritaniDepartment of Pathology, Shiga Medical University, Otsu, Shiga, Japan.
Tomonori KawasakiDepartment of Molecular Diagnostic Pathology, Iwate Medical University School of Medicine, Morioka, Japan.
Tomoko UchiyamaDepartment of Pathology, Nara Medical University, Kashihara, Nara, Japan.
Hiroe ItamiDepartment of Pathology, Nara Medical University, Kashihara, Nara, Japan.
Kouhei MoritaDepartment of Pathology, Nara Medical University, Kashihara, Nara, Japan.
Masato TakanoDepartment of Pathology, Nara Medical University, Kashihara, Nara, Japan.
Maiko TakedaDepartment of Pathology, Nara Medical University, Kashihara, Nara, Japan.
Kinta HatakeyamaDepartment of Pathology, Nara Medical University, Kashihara, Nara, Japan.
Chiho OhbayashiDepartment of Pathology, Nara Medical University, Kashihara, Nara, Japan.
Nara Medical University · JPNagoya Medical Center · JPIwate Medical University · JPShiga University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adenoid cystic carcinoma (AdCC) of the breast is an uncommon but distinct neoplasm composed of a dual cell population polarized around true glandular (luminal) spaces and pseudolumina. The aim of this study was to clarify whether various immunohistochemical markers (CK7, EMA, CD117, p63, calponin, CD10, S100, CK5/6, CK14, vimentin, and type IV collagen) can distinguish between the two cell types in classical AdCC (n = 14) and in collagenous spherulosis (n = 5). The sensitivity and specificity of these 11 markers to distinguish luminal from abluminal cells were evaluated using a curve created by plotting the true-positive rate (sensitivity) against the false-positive rate (1 - specificity) at threshold settings of 0, 10, 50, and 70 %. The most sensitive and specific markers for luminal cells in AdCC were CK7 and EMA; those for abluminal cells were type IV collagen, p63, and vimentin. CD10 and S100 did not act as abluminal markers in AdCC. CK5/6, one of the basal/myoepithelial markers, was expressed more frequently in luminal than in abluminal cells of AdCC. Thus, CK5/6 immunostaining resulted in a reverse expression pattern, analogous to what we recently documented in clear cells in mammary adenomyoepithelioma. In conclusion, compared with myoepithelial/abluminal cells of normal breast or collagenous spherulosis, the neoplastic abluminal cells of classical AdCC are characterized by enhanced vimentin and attenuated CD10 and S100. Furthermore, the luminal cells of AdCC show a unique aberrant staining pattern for CK5/6 that may aid in the differential diagnosis.

Indexed as

AdenomyoepitheliomaAgedAged, 80 and overBiomarkers, TumorBreast NeoplasmsCarcinoma, Adenoid CysticDiagnosis, DifferentialEpithelial CellsFemaleHumansImmunohistochemistryKeratin-5Keratin-6Middle AgedMyoepitheliomaBiomarkers, TumorKeratin-5Keratin-6Adenoid cystic carcinomaCollagenous spherulosisCytokeratin 5/6Myoepithelial cellsVimentin

Identifiers

PMID27240462
OpenAlexW2414038052

What OpenQuestion holds

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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.