Evidence map›Paper›PMID 22179180›Full record

ReviewMedical molecular morphology2011

Sorafenib: complexities of Raf-dependent and Raf-independent signaling are now unveiled.

Yasunobu Matsuda, Manabu Fukumoto

Abstract readReview
PubMed Publisher
In one paragraph

Review in Medical molecular morphology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
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  4. Host-Directed Antiviral Therapy.Clinical microbiology reviews · 2020
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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.

Yasunobu MatsudaDepartment of Medical Technology, Niigata University Graduate School of Health Sciences, Asahimachi-dori, Niigata, Japan. yasunobu@med.niigata-u.ac.jp
Manabu Fukumoto
Niigata University · JPTohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common primary cancer worldwide. The only current drug available for clinical treatment of HCC is sorafenib, which inhibits multiple signaling kinases including Raf family members, platelet-derived growth factor receptor, vascular endothelial growth factor receptors 1 and 2, c-Kit, and Fms-like tyrosine kinase 3. Many studies have revealed that the mechanism underlying the antitumor effect of sorafenib is complex. Because sorafenib inhibits C-Raf more potently than B-Raf, the therapeutic efficacy of sorafenib is strongly influenced by the relative expression and activity of B-Raf and C-Raf and the complex interactions between these factors. Moreover, Rafindependent signaling mechanisms have recently emerged as important pathways of sorafenib-induced cell death. Basic research studies have suggested that using sorafenib as part of a combination therapy may improve its effect, although this has yet to be confirmed by clinical evidence. Further studies of the functional mechanism of sorafenib are required to advance the development of targeted therapy for HCC. To aid future work on sorafenib, we here review the current literature pertaining to sorafenib signaling and its clinical efficacy in both monotherapy and combination therapy.

Indexed as

Antineoplastic AgentsBenzenesulfonatesCarcinoma, HepatocellularDrug SynergismEndoplasmic Reticulum StressHumansLiver NeoplasmsMAP Kinase Signaling SystemMyeloid Cell Leukemia Sequence 1 ProteinNeovascularization, PathologicNiacinamidePhenylurea CompoundsProto-Oncogene Proteins c-bcl-2Pyridinesraf KinasesSorafenibAntineoplastic AgentsBenzenesulfonatesMyeloid Cell Leukemia Sequence 1 ProteinNiacinamidePhenylurea CompoundsProto-Oncogene Proteins c-bcl-2Pyridinesraf KinasesSorafenib

Identifiers

PMID22179180
OpenAlexW2092008268

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.