Evidence map›Paper›PMID 12439752›Full record

ArticleOncogene2002

Long-term tumor-free survival from treatment with the GFP-TRAIL fusion gene expressed from the hTERT promoter in breast cancer cells.

Tongyu Lin, Xuefeng Huang, Jian Gu, Lidong Zhang, Jack A Roth, Momiao Xiong, Steven A Curley, Yinhua Yu, Kelly K Hunt, Bingliang Fang

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 110 citations in OpenAlex.

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  10. Targeted expression of miR-34a using the T-VISA system suppresses breast cancer cell growth and invasion.Molecular therapy : the journal of the American Society of Gene Therapy · 2012
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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

10 authors at 4 institutions in 1 country.

Tongyu LinDepartment of Thoracic and Cardiovascular Surgery, Section of Thoracic Molecular Oncology, The University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.
Xuefeng Huang
Jian Gu
Lidong Zhang
Jack A Roth
Momiao Xiong
Steven A Curley
Yinhua Yu
Kelly K Hunt
Bingliang Fang
The University of Texas MD Anderson Cancer Center · USCancer Support Community · USMolecular Oncology (United States) · USThoracic Surgery Foundation · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS CA16672
6 · The paper itself

Abstract

We evaluated anti-tumor activity and toxic effect of an adenoviral vector expressing the GFP/TRAIL fusion gene from the hTERT promoter (designated Ad/gTRAIL) on human breast cancer cell lines and on normal human breast cells. Treatment with Ad/gTRAIL elicited high levels of transgene expression and apoptosis in a variety of breast cancer cell lines. Furthermore, treatment with Ad/gTRAIL was effective in killing breast cancer lines resistant to doxorubicin or soluble TRAIL protein. In contrast, only minimal transgene expression and toxicity was detected in normal human primary mammary epithelial cells after treatment with this vector. An in vivo study further showed that the intralesional administration of Ad/gTRAIL effectively suppressed the growth of human tumor xenografts derived from both doxorubicin-sensitive and doxorubicin-resistant breast cancer lines. Specifically, about 50% of animals bearing doxorubicin-sensitive and doxorubicin-resistant breast cancer xenografts showed complete tumor regression and remained tumor-free for over 5 months. These results suggest that the adenovirus encoding the GFP/TRAIL gene driven by the hTERT promoter has potential application in cancer therapy.

Indexed as

Genetic TherapyPromoter Regions, GeneticApoptosis Regulatory ProteinsBreast NeoplasmsDisease-Free SurvivalDNA-Binding ProteinsGreen Fluorescent ProteinsHumansIn Situ Nick-End LabelingLuminescent ProteinsMembrane GlycoproteinsRecombinant Fusion ProteinsTelomeraseTNF-Related Apoptosis-Inducing LigandTumor Cells, CulturedTumor Necrosis Factor-alphaApoptosis Regulatory ProteinsDNA-Binding ProteinsGreen Fluorescent ProteinsLuminescent ProteinsMembrane GlycoproteinsRecombinant Fusion ProteinsTelomeraseTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID12439752
OpenAlexW2011798442

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.