Evidence map›Paper›PMID 23150447›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2013

Isolation and characterization of murine multipotent lung stem cells.

Venkat S Gadepalli, Catherine Vaughan, Raj R Rao

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
11.8field-weighted citation impact, top 2% 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

8 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Piezo1 mediates angiogenesis through activation of MT1-MMP signaling.American journal of physiology. Cell physiology · 2019
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Lung stem and progenitor cells.Respiration; international review of thoracic diseases · 2013
    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

3 authors at 1 institution in 1 country.

Venkat S GadepalliIntegrative Life Sciences, Department of Life Sciences, Virginia Commonwealth University, Richmond, VA, USA.
Catherine Vaughan
Raj R Rao
Virginia Commonwealth University · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Keri R Maher · 1985 to 2026
$51.0M
Chemoresistance and Motility: Role of Mutant p53 and NF-kB2 in CancerR01CA121144 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI DEB, SUMITRA · 2008 to 2011
$1.0M
NCI NIH HHS P30 CA016059NCI NIH HHS R01 CA121144
6 · The paper itself

Abstract

Cancer stem cells possess the ability to self-renew and differentiate into specific cells found in tumor types, a characteristic feature of normal multipotent stem cells. These cells harbor within the bulk of tumors and if the tumor suppressor p53 is mutated in these cells, can be more likely to cause relapse and metastasis by giving rise to new tumors. This new paradigm of oncogenesis has been observed in various cancers, including lung cancer. Determining the interaction of critical cellular pathways in the ontogeny of lung tumors is expected to lead to identification of molecular targets for effective therapeutic strategies. To achieve this, it is important to characterize and dissect the differences between the cancer cells with aberrant stem cell like properties and normal multipotent stem cells that contribute to regeneration. This could be accomplished by using cell surface markers unique for certain cell types by employing techniques such as flow cytometry and magnetic bead isolation. This chapter summarizes the isolation process of the resident stem cell Sca1 (+ve), CD-45 (-ve), and CD-31 (-ve) populations for its potential use in assessing correlations between specific p53 gain of function phenotypes in different murine lung cancer models.

Indexed as

AnimalsCell Transformation, NeoplasticFlow CytometryLungLung NeoplasmsMiceNeoplastic Stem CellsPhenotypePluripotent Stem CellsTumor Suppressor Protein p53Tumor Suppressor Protein p53

Identifiers

PMID23150447
PMCPMC4844181
OpenAlexW2414391493

What OpenQuestion holds

Textmetadata
LicenceTDM
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.