Evidence map›Paper›PMID 8391215›Full record

ArticleThe American journal of pathology1993

Nuclear A-type lamins are differentially expressed in human lung cancer subtypes.

J L Broers, Y Raymond, M K Rot, H Kuijpers, S S Wagenaar, F C Ramaekers

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In one paragraph

Article in The American journal of pathology, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

71 citing papers in PubMed, 141 citations in OpenAlex.

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  15. The Role of Emerin in Cancer Progression and Metastasis.International journal of molecular sciences · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Nesprin-1 impact on tumorigenic cell phenotypes.Molecular biology reports · 2020
    Article

11 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

J L BroersDepartment of Molecular Cell Biology & Genetics, University of Limburg, Maastricht, The Netherlands.
Y Raymond
M K Rot
H Kuijpers
S S Wagenaar
F C Ramaekers
Maastricht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear A-type and B-type lamin expression was investigated in the major human lung cancer subtypes: small cell lung cancer (SCLC), squamous cell carcinomas, and adenocarcinomas (both non-SCLC). Twenty-two human lung cancer cell lines and 46 fresh frozen human lung cancer specimens were examined. Expression of B-type lamins was found in all the different cell lines. A-type lamins were expressed in all non-SCLC cell lines but were absent or only weakly expressed in 14 out of 16 SCLC cell lines. The immunocytochemical results were confirmed by immunoblotting and Northern blot analyses. In sections of SCLCs and non-SCLCs, B-type lamins were found to be expressed in all tumors. However, in some non-SCLCs, particularly in adenocarcinomas, a considerable proportion of the tumor cells were negative for B-type lamins. A-type lamin expression in SCLCs was weakly positive or negative in 14 out of 15 cases. In contrast, all non-SCLCs displayed A-type lamins, but in several of these samples, both cytoplasmic and nuclear staining was observed.

Indexed as

AdenocarcinomaBlotting, NorthernCarcinoma, Non-Small-Cell LungCarcinoma, Small CellCarcinoma, Squamous CellElectrophoresis, Polyacrylamide GelFrozen SectionsHumansImmunoblottingImmunohistochemistryLaminsLung NeoplasmsNuclear ProteinsTumor Cells, CulturedLaminsNuclear Proteins

Identifiers

PMID8391215
PMCPMC1886958
OpenAlexW1553065669

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.