Evidence map›Paper›PMID 24970164›Full record

ArticleBiomolecules2013

Multi-Color Spectral Transcript Analysis (SPECTRA) for Phenotypic Characterization of Tumor Cells.

Joanne H Hsu, Jingly F Weier, Heinz-Ulrich G Weier, Yuko Ito

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 89% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 4 institutions in 2 countries.

Joanne H HsuFred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle, WA 98109, USA. jhhsu11@gmail.com.
Jingly F WeierLife Sciences Division, E.O. Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA. jinglyw@gmail.com.
Heinz-Ulrich G WeierLife Sciences Division, E.O. Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA. ugweier@lbl.gov.
Yuko ItoNational Institute of Science and Technology Policy (NISTEP), Ministry of Education, Culture, Sports, Science and Technology, Tokyo 100-0005, Japan. itoh@nistep.go.jp.
Fred Hutch Cancer Center · USLawrence Berkeley National Laboratory · USNational Institute of Science and Technology Policy · JPUniversity of California, San Francisco · US

Funding

Radiation-induced Thyroid CancerR01CA136685 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI WEIER, HEINZ-ULRICH GUENTER · 2009 to 2011
$1.1M
Aneuploid Cells in the Human PlacentaR01HD045736 · NICHD · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI WEIER, HEINZ-ULRICH G. · 2004 to 2006
$969k
Full karyotype single cell interphase analysisR44HD044313 · NICHD · REPROGENETICS, INC. · PI MUNNE, SANTIAGO · 2003 to 2005
$712k
NCI NIH HHS R01 CA136685NICHD NIH HHS R01 HD045736NICHD NIH HHS R44 HD044313
6 · The paper itself

Abstract

Many human tumors show significant changes in their signal transduction pathways and, thus, the way the cells interact with their environment. Often caused by chromosomal rearrangements, including gene amplifications, translocations or deletions, the altered levels of gene expression may provide a tumor-specific signature that can be exploited for diagnostic or therapeutic purposes. We investigated the utility of multiplexed fluorescence in situ hybridization (FISH) using non-isotopically labeled cDNA probes detected by Spectral Imaging as a sensitive and rapid procedure to measure tumor-specific gene expression signatures. We used a commercially available system to acquire and analyze multicolor FISH images. Initial investigations used panels of fluorescent calibration standards to evaluate the system. These experiments were followed by hybridization of five-to-six differently labeled cDNA probes, which target the transcripts of tyrosine kinase genes known to be differently expressed in normal cells and tumors of the breast or thyroid gland. The relatively simple, yet efficient, molecular cytogenetic method presented here may find many applications in characterization of solid tumors or disseminated tumor cells. Addressing tumor heterogeneity by means of multi-parameter single cell analyses is expected to enable a wide range of investigations in the areas of tumor stem cells, tumor clonality and disease progression.

Identifiers

PMID24970164
PMCPMC4030878
OpenAlexW2134583266

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.