Evidence map›Paper›PMID 27133774›Full record

ReviewJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2016

Is the Canonical RAF/MEK/ERK Signaling Pathway a Therapeutic Target in SCLC?

Sandra Cristea, Julien Sage

Open access · greenAbstract readReview
In one paragraph

Review in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 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 1 institution in 1 country.

Sandra CristeaDepartment of Pediatrics, Stanford University, Stanford, California; Department of Genetics, Stanford University, Stanford, California.
Julien SageDepartment of Pediatrics, Stanford University, Stanford, California; Department of Genetics, Stanford University, Stanford, California. Electronic address: julsage@stanford.edu.
Stanford University · US

Funding

Molecular and cellular mechanisms of SCLC metastasisR01CA206540 · NCI · STANFORD UNIVERSITY · PI SAGE, JULIEN · 2016 to 2019
$1.7M
Notch signaling in small cell lung carcinomaR01CA201513 · NCI · STANFORD UNIVERSITY · PI SAGE, JULIEN · 2016 to 2019
$1.5M
NCI NIH HHS R01 CA201513NCI NIH HHS R01 CA206540
6 · The paper itself

Abstract

The activity of the RAF/MEK/ERK signaling pathway is critical for the proliferation of normal and cancerous cells. Oncogenic mutations driving the development of lung adenocarcinoma often activate this signaling pathway. In contrast, pathway activity levels and their biological roles are not well established in small cell lung cancer (SCLC), a fast-growing neuroendocrine lung cancer subtype. Here we discuss the function of the RAF/MEK/ERK kinase pathway and the mechanisms leading to its activation in SCLC cells. In particular, we argue that activation of this pathway may be beneficial to the survival, proliferation, and spread of SCLC cells in response to multiple stimuli. We also consider evidence that high levels of RAF/MEK/ERK pathway activity may be detrimental to SCLC tumors, including in part by interfering with their neuroendocrine fate. On the basis of these observations, we examined when small molecules targeting kinases in the RAF/MEK/ERK pathway may be useful therapeutically in patients with SCLC, including in combination with other therapeutic agents.

Indexed as

Extracellular Signal-Regulated MAP KinasesHumansLung NeoplasmsMAP Kinase Signaling SystemMitogen-Activated Protein Kinase KinasesNeoplasm Metastasisraf KinasesSignal TransductionSmall Cell Lung CarcinomaExtracellular Signal-Regulated MAP KinasesMitogen-Activated Protein Kinase Kinasesraf KinasesCombination therapyERK1/2GPCRMAPKSCLCSignaling

Identifiers

PMID27133774
PMCPMC5391975
OpenAlexW2344677018

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.