Evidence map›Paper›PMID 23211466›Full record

ArticleOncotarget2012

Targeting MCT-1 oncogene inhibits Shc pathway and xenograft tumorigenicity.

Hung-Ju Shih, Hsiao-Huei Chen, Yen-An Chen, Meng-Hsun Wu, Gan-Guang Liou, Wei-Wen Chang, Linyi Chen, Lu-Hai Wang, Hsin-Ling Hsu

Open access · hybridAbstract read
In one paragraph

Article in Oncotarget, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

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  14. Systemic delivery of microencapsulated 3-bromopyruvate for the therapy of pancreatic cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2014
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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

9 authors at 3 institutions in 1 country.

Hung-Ju ShihInstitute of Molecular and Genomic Medicine, National Health Research Institutes, Taiwan.
Hsiao-Huei Chen
Yen-An Chen
Meng-Hsun Wu
Gan-Guang Liou
Wei-Wen Chang
Linyi Chen
Lu-Hai Wang
Hsin-Ling Hsu
National Health Research Institutes · TWNational Tsing Hua University · TWWan Fang Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of Shc adaptor proteins is associated with mitogenesis, carcinogenesis and metastasis. Multiple copies in T-cell malignancy 1 (MCT-1) oncoprotein promotes cell proliferation, survival and tumorigenic effects. Our current data show that MCT-1 is a novel regulator of Shc-Ras-MEK-ERK signaling and MCT-1 is significantly co-activated with Shc gene in human carcinomas. The knockdown of MCT-1 enhances apoptotic cell death accompanied with the activation of caspases and cleavage of caspase substrates under environmental stress. The cancer cell proliferation, chemo-resistance and tumorigenic capacity are proved to be effectively suppressed by targeting MCT-1. Accordingly, an important linkage between MCT-1 oncogenicity and Shc pathway in tumor development has now been established. Promoting MCT-1 expression by gene hyperactivation may be recognized as a tumor marker and MCT-1 may serve as a molecular target of cancer therapy.

Indexed as

AnimalsApoptosisBreast NeoplasmsCaspase 3Cell Cycle ProteinsCell Growth ProcessesCell Line, TumorFemaleGene Knockdown TechniquesHumansImmunohistochemistryIntegrin beta4Lung NeoplasmsMAP Kinase Signaling SystemMiceMice, Inbred BALB CCaspase 3Cell Cycle ProteinsIntegrin beta4MCTS1 protein, humanOncogene ProteinsPaclitaxelPoly(ADP-ribose) Polymerasesras ProteinsRNA, MessengerShc Signaling Adaptor Proteins

Identifiers

PMID23211466
PMCPMC3717801
OpenAlexW2114062089

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.