Evidence map›Paper›PMID 29440321›Full record

ReviewCold Spring Harbor perspectives in medicine2018

Targeting the MAPK Pathway in RAS Mutant Cancers.

Sarah G Hymowitz, Shiva Malek

Open access · bronzeAbstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 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 2 countries.

Sarah G HymowitzDepartment of Structural Biology, Genentech Inc., South San Francisco, California 94080.
Shiva MalekDepartment of Discovery Oncology, Genentech Inc., South San Francisco, California 94080.
Discovery Centre · CAInstitute for Structural Research · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite decades of extensive drug discovery efforts, there are currently no targeted therapies approved to treat KRAS mutant cancers. In this review, we highlight the challenges and opportunities in targeting KRAS mutant tumors through inhibition of mitogen-activated protein kinase (MAPK) signaling with conformation-specific kinase inhibitors. Through structural analysis and mechanistic studies with BRAF and mitogen-activated protein kinase (MEK) inhibitors, we describe how kinase-dependent and -independent functions of MAPK signaling components regulate KRAS-driven tumorigenesis and how these insights can be used to treat RAS mutant cancers with small molecule kinase inhibitors.

Indexed as

Antineoplastic AgentsExtracellular Signal-Regulated MAP KinasesGenes, rasHumansMAP Kinase Kinase KinasesMAP Kinase Signaling SystemMitogen-Activated Protein KinasesMutationNeoplasmsProto-Oncogene Proteins B-rafraf KinasesAntineoplastic AgentsExtracellular Signal-Regulated MAP KinasesMAP Kinase Kinase KinasesMitogen-Activated Protein KinasesProto-Oncogene Proteins B-rafraf Kinases

Identifiers

PMID29440321
PMCPMC6211377
OpenAlexW2787439801

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.