Evidence map›Paper›PMID 12545165›Full record

ArticleOncogene2003

DLC-1 gene inhibits human breast cancer cell growth and in vivo tumorigenicity.

Bao-Zhu Yuan, Xiaoling Zhou, Marian E Durkin, Drazen B Zimonjic, Katrin Gumundsdottir, Jorunn E Eyfjord, Snorri S Thorgeirsson, Nicholas C Popescu

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

68 citing papers in PubMed, 153 citations in OpenAlex.

  1. Article
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  8. Article
  9. Estrogen receptor signaling is reprogrammed during breast tumorigenesis.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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8 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

8 authors at 3 institutions in 2 countries.

Bao-Zhu YuanLaboratory of Experimental Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA.
Xiaoling Zhou
Marian E Durkin
Drazen B Zimonjic
Katrin Gumundsdottir
Jorunn E Eyfjord
Snorri S Thorgeirsson
Nicholas C Popescu
National Cancer Institute · USCenter for Cancer Research · USIcelandic Cancer Society · IS

Funding

Molecular Cytogenetics of Solid TumorsZIABC010038 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POPESCU, NICOLAE · 2009 to 2012
$4.5M
MOLECULAR CYTOGENETICS OF SOLID TUMORSZ01BC010038 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POPESCU, NICOLAE · 1996 to 2008
$2.3M
6 · The paper itself

Abstract

The human DLC-1 (deleted in liver cancer 1) gene was cloned from a primary human hepatocellular carcinoma (HCC) and mapped to the chromosome 8p21-22 region frequently deleted in common human cancers and suspected to harbor tumor suppressor genes. DLC-1 was found to be deleted or downregulated in a significant number of HCCs. We expanded our investigations to other cancers with recurrent deletions of 8p22, and in this study examined alterations of DLC-1 in primary human breast tumors, human breast, colon, and prostate tumor cell lines. Genomic deletion of DLC-1 was observed in 40% of primary breast tumors, whereas reduced or undetectable levels of DLC-1 mRNA were seen in 70% of breast, 70% of colon, and 50% of prostate tumor cell lines To see whether DLC-1 expression affects cell growth and tumorigenicity, two breast carcinoma cell lines lacking the expression of endogenous gene were transfected with the DLC-1 cDNA. In both cell lines, DLC-1 transfection caused significant growth inhibition and reduction of colony formation. Furthermore, introduction of the DLC-1 cDNA abolished the in vivo tumorigenicity in nude mice, suggesting that the DLC-1 gene plays a role in breast cancer by acting as a bona fide tumor suppressor gene.

Indexed as

AdenocarcinomaAnimalsBreast NeoplasmsCarcinogenicity TestsCell DivisionColonic NeoplasmsFemaleGene DeletionGene Expression Regulation, NeoplasticGTPase-Activating ProteinsHumansMaleMammary Neoplasms, ExperimentalMiceMice, Inbred BALB CProstatic NeoplasmsDLC1 protein, humanGTPase-Activating ProteinsTumor Suppressor Proteins

Identifiers

PMID12545165
OpenAlexW2017541958

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.