Evidence map›Paper›PMID 31137846›Full record

ArticleCells2019

Inhibition of Hedgehog Signaling in Fibroblasts, Pancreatic, and Lung Tumor Cells by Oxy186, an Oxysterol Analogue with Drug-Like Properties.

Feng Wang, Frank Stappenbeck, Farhad Parhami

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
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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

3 authors at 1 institution in 1 country.

Feng WangMAX BioPharma Inc., 2870 Colorado Avenue, Santa Monica, CA 90404, USA. fwang@maxbiopharma.com.
Frank StappenbeckMAX BioPharma Inc., 2870 Colorado Avenue, Santa Monica, CA 90404, USA. fstappenbeck@maxbiopharma.com.
Farhad ParhamiMAX BioPharma Inc., 2870 Colorado Avenue, Santa Monica, CA 90404, USA. fparhami@maxbiopharma.com.
Max Biopharma (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The widespread involvement of the Hedgehog (Hh) signaling pathway in human malignancies has motivated the clinical development of Smoothened (Smo) antagonists, such as vismodegib and sonidegib. However, Smo antagonists have failed to benefit patients suffering from Hh pathway-dependent solid tumors, such as pancreatic, colorectal, or ovarian cancer. Hh-dependent cancers are often driven by activating mutations that occur downstream of Smo and directly activate the transcription factors known as glioma-associated oncogenes (

Indexed as

A549 CellsAnimalsArea Under CurveCell ProliferationFibroblastsHalf-LifeHedgehog ProteinsHep G2 CellsHumansLiver X ReceptorsLung NeoplasmsMiceMice, Inbred BALB CNIH 3T3 CellsOxysterolsPancreatic NeoplasmsGLI1 protein, humanHedgehog ProteinsLiver X ReceptorsOxysterolsPhenanthrenesPregnenoloneSmoothened ReceptorZinc Finger Protein GLI1cancerhedgehog signalingnon-canonical activation of Glioxysterols

Identifiers

PMID31137846
PMCPMC6562610
OpenAlexW2945834009

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.