Evidence map›Paper›PMID 31201505›Full record

ArticleVirchows Archiv : an international journal of pathology2019

Constitutional abnormality of nuclear membrane proteins in small cell lung carcinoma.

Jieying Wang, Tetsuo Kondo, Tadao Nakazawa, Naoki Oishi, Kunio Mochizuki, Ryohei Katoh

Abstract read
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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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

6 authors at 2 institutions in 2 countries.

Jieying WangDepartment of Pathology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chyuo-shi, Yamanashi, 409-3898, Japan. wangjieying1234@163.com.ORCID http://orcid.org/0000-0001-7339-2744
Tetsuo KondoDepartment of Pathology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chyuo-shi, Yamanashi, 409-3898, Japan.
Tadao NakazawaDepartment of Pathology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chyuo-shi, Yamanashi, 409-3898, Japan.
Naoki OishiDepartment of Pathology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chyuo-shi, Yamanashi, 409-3898, Japan.
Kunio MochizukiDepartment of Pathology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chyuo-shi, Yamanashi, 409-3898, Japan.
Ryohei KatohDepartment of Pathology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chyuo-shi, Yamanashi, 409-3898, Japan.
University of Yamanashi Hospital · JPXi'an Medical University · CN

Funding

Natural Science Foundation of Shaanxi Provincial Department of Education 18JK0666
6 · The paper itself

Abstract

Nuclear membrane proteins reportedly play important roles in maintaining nuclear structures and coordinating cell activities. Studying profiles of nuclear membrane proteins may help us evaluate the biological and/or clinical nature of malignant tumors. Using immunohistochemistry with antibodies for emerin, lamin A/C, lamin B, and LAP2, we examined 105 lung cancer tissues from 33 small cell lung carcinomas (SCLCs) and 72 non-SCLCs (34 adenocarcinomas, 30 squamous cell carcinomas, and 8 large cell carcinomas). Emerin had negative or local/weak positivity in 79% of SCLCs and 1% of non-SCLCs, and lamin A/C had similar positivity in 91% of SCLCs and 3% of non-SCLCs. LAP2's expression was similar between SCLCs and non-SCLCs. RT-PCR analyses for these four nuclear membrane proteins over 7 cell lines showed that mRNA of emerin and lamin A/C were distinctly downregulated in the SCLC cell lines, supporting the immunohistochemical results. In conclusion, we suggest that downregulation of the nuclear membrane proteins emerin and lamin A/C is characteristic of SCLC cells, and this constitutional abnormality of the nuclear membrane may be related to the biological and/or clinical nature of SCLC. In addition, knowing the nuclear protein profile in SCLC cells may contribute to our understanding of nuclear fragility known as the crush artifact in pulmonary biopsy specimens.

Indexed as

Biomarkers, TumorDNA-Binding ProteinsHumansLamin Type ALamin Type BLung NeoplasmsMembrane ProteinsNuclear ProteinsSmall Cell Lung CarcinomaBiomarkers, TumorDNA-Binding Proteinsemerinlamina-associated polypeptide 2Lamin Type ALamin Type BMembrane ProteinsNuclear ProteinsImmunohistochemistryLung carcinomaNuclear membrane proteinsPolymerase chain reaction (PCR)

Identifiers

PMID31201505
OpenAlexW2950545462

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.