Evidence map›Paper›PMID 24482735›Full record

ReviewAmerican journal of cancer research2014

Beyond laser microdissection technology: follow the yellow brick road for cancer research.

Luc G Legres, Anne Janin, Christophe Masselon, Philippe Bertheau

Abstract readReview
In one paragraph

Review in American journal of cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
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  15. Article
  16. Toward precision medicine of breast cancer.Theoretical biology & medical modelling · 2016
    Review
  17. Article
  18. Review
  19. Review
  20. Mammary stem cells: expansion and animal productivity.Journal of animal science and biotechnology · 2014
    Review
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

4 authors.

Luc G LegresInserm UMR_S1165, Institut Universitaire d'Hématologie Paris ; Université Paris-Diderot Paris.
Anne JaninInserm UMR_S1165, Institut Universitaire d'Hématologie Paris ; Université Paris-Diderot Paris ; AP-HP, Hôpital Saint-Louis, Service de Pathologie Paris.
Christophe MasselonCEA, iRTSV/Laboratoire de Biologie à Grande Echelle Grenoble ; Inserm UMR_S 1038 Grenoble.
Philippe BertheauInserm UMR_S1165, Institut Universitaire d'Hématologie Paris ; Université Paris-Diderot Paris ; AP-HP, Hôpital Saint-Louis, Service de Pathologie Paris.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Normal biological tissues harbour different populations of cells with intricate spacial distribution patterns resulting in heterogeneity of their overall cellular composition. Laser microdissection involving direct viewing and expertise by a pathologist, enables access to defined cell populations or specific region on any type of tissue sample, thus selecting near-pure populations of targeted cells. It opens the way for molecular methods directed towards well-defined populations, and provides also a powerful tool in studies focused on a limited number of cells. Laser microdissection has wide applications in oncology (diagnosis and research), cellular and molecular biology, biochemistry and forensics for tissue selection, but other areas have been gradually opened up to these new methodological approaches, such as cell cultures and cytogenetics. In clinical oncology trials, molecular profiling of microdissected samples can yield global "omics" information which, together, with the morphological analysis of cells, can provide the basis for diagnosis, prognosis and patient-tailored treatments. This remarkable technology has brought new insights in the understanding of DNA, RNA, and the biological functions and regulation of proteins to identify molecular disease signatures. We review herein the different applications of laser microdissection in a variety of fields, and we particularly focus attention on the pre-analytical steps that are crucial to successfully perform molecular-level investigations.

Indexed as

DNAhistopathologyin situ cellular and molecular analysesLaser microdissectionproteomicsquality controlRNAsnap-freezing

Identifiers

PMID24482735
PMCPMC3902229

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.