Evidence map›Paper›PMID 29203271›Full record

ReviewSeminars in cancer biology2019

Concepts and advances in cancer therapeutic vulnerabilities in RAS membrane targeting.

James V Michael, Lawrence E Goldfinger

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cancer biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

James V MichaelThe Sol Sherry Thrombosis Research Center, Department of Anatomy & Cell Biology, Lewis Katz School of Medicine at Temple University, Cancer Biology Program, Fox Chase Cancer Center, Philadelphia, PA, 19140 USA.
Lawrence E GoldfingerThe Sol Sherry Thrombosis Research Center, Department of Anatomy & Cell Biology, Lewis Katz School of Medicine at Temple University, Cancer Biology Program, Fox Chase Cancer Center, Philadelphia, PA, 19140 USA. Electronic address: goldfinger@temple.edu.
Fox Chase Cancer Center · USTemple University · US

Funding

Novel small G protein pathway regulators of GPVI signaling in plateletsR01HL137207 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI GOLDFINGER, LAWRENCE E, KUNAPULI, SATYA P. · 2017 to 2020
$2.5M
NHLBI NIH HHS R01 HL137207
6 · The paper itself

Abstract

For decades oncogenic RAS proteins were considered undruggable due to a lack of accessible binding pockets on the protein surfaces. Seminal early research in RAS biology uncovered the basic paradigm of post-translational isoprenylation of RAS polypeptides, typically with covalent attachment of a farnesyl group, leading to isoprenyl-mediated RAS anchorage at the plasma membrane and signal initiation at those sites. However, the failure of farnesyltransferase inhibitors to translate to the clinic stymied anti-RAS therapy development. Over the past ten years, a more complete picture has emerged of RAS protein maturation, intracellular trafficking, and location, positioning and retention in subdomains at the plasma membrane, with a corresponding expansion in our understanding of how these properties of RAS contribute to signal outputs. Each of these aspects of RAS regulation presents a potential vulnerability in RAS function that may be exploited for therapeutic targeting, and inhibitors have been identified or developed that interfere with RAS for nearly all of them. This review will summarize current understanding of RAS membrane targeting with a focus on highlighting development and outcomes of inhibitors at each step.

Indexed as

AnimalsAntineoplastic AgentsCell MembraneGalectinsHumansMembrane MicrodomainsMolecular Targeted TherapyMutationNeoplasmsOncogene ProteinsProtein BindingProteolysisras ProteinsAntineoplastic AgentsGalectinsOncogene Proteinsras ProteinsGalectinLipid raftsPlasma membraneRASTherapeutics

Identifiers

PMID29203271
PMCPMC5984110
OpenAlexW2775307197

What OpenQuestion holds

Textmetadata
LicenceTDM
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.