Evidence map›Paper›PMID 18440854›Full record

ReviewDrug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy2008

Role of mTOR in anticancer drug resistance: perspectives for improved drug treatment.

Bing-Hua Jiang, Ling-Zhi Liu

Open access · greenAbstract readReview
In one paragraph

Review in Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed, 1 pooled it
9.4field-weighted citation impact, top 1% 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

128 citing papers in PubMed, 1 synthesis or guideline pooled it, 240 citations in OpenAlex.

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  14. Genomic Landscape and Potential Regulation of RNA Editing in Drug Resistance.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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68 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

2 authors at 2 institutions in 1 country.

Bing-Hua JiangDepartment of Microbiology, Mary Babb Randolph Cancer Center, Immunology and Cell Biology, West Virginia University, Morgantown, WV 26506, USA. bhjiang@hsc.wvu.edu
Ling-Zhi Liu
West Virginia University · USWest Virginia University Hospitals · US

Funding

THE ROLE OF HEF1 PROTEIN IN INVASION OF METASTATIC BREAST CANCERP20RR016440 · NCRR · WEST VIRGINIA UNIVERSITY · PI GRABER, STEPHEN G · 2001 to 2010
$22.8M
PI3K Pathway in Prostate Tumorigenesis and AngiogenesisR01CA109460 · NCI · WEST VIRGINIA UNIVERSITY · PI JIANG, BINGHUA · 2006 to 2010
$1.2M
Analysis of Apigenin in Inhibiting Ovarian TumorigenesisR03CA123675 · NCI · WEST VIRGINIA UNIVERSITY · PI JIANG, BINGHUA · 2006 to 2007
$144k
NCI NIH HHS CA109460NCI NIH HHS CA123675NCI NIH HHS R01 CA109460NCI NIH HHS R03 CA123675NCRR NIH HHS P20 RR016440
6 · The paper itself

Abstract

The mammalian target of rapamycin (mTOR) pathway plays a central role in regulating protein synthesis, ribosomal protein translation, and cap-dependent translation. Deregulations in mTOR signaling are frequently associated with tumorigenesis, angiogenesis, tumor growth and metastasis. This review highlights the role of the mTOR in anticancer drug resistance. We discuss the network of signaling pathways in which the mTOR kinase is involved, including the structure and activation of the mTOR complex and the pathways upstream and downstream of mTOR as well as other molecular interactions of mTOR. Major upstream signaling components in control of mTOR activity are PI3K/PTEN/AKT and Ras/Raf/MEK/ERK pathways. We discuss the central role of mTOR in mediating the translation of mRNAs of proteins related to cell cycle progression, those involved in cell survival such as c-myc, hypoxia inducible factor 1* (HIF-1*) and vascular endothelial growth factor (VEGF), cyclin A, cyclin dependent kinases (cdk1/2), cdk inhibitors (p21(Cip1) and p27(Kip1)), retinoblastoma (Rb) protein, and RNA polymerases I and III. We then discuss the potential therapeutic opportunities for using mTOR inhibitors rapamycin, CCI-779, RAD001, and AP-23573 in cancer therapy as single agents or in combinations to reverse drug resistance.

Indexed as

Antineoplastic AgentsApoptosisCell CycleDrug Resistance, NeoplasmHumansNeoplasmsProtein BiosynthesisProtein ConformationProtein Kinase InhibitorsProtein KinasesSignal TransductionTOR Serine-Threonine KinasesAntineoplastic AgentsMTOR protein, humanProtein Kinase InhibitorsProtein KinasesTOR Serine-Threonine Kinases

Identifiers

PMID18440854
PMCPMC2519122
OpenAlexW1988976358

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.