Evidence map›Paper›PMID 18408751›Full record

ArticleOncogene2008

The BH3-only member Noxa causes apoptosis in melanoma cells by multiple pathways.

M Hassan, A Alaoui, O Feyen, A Mirmohammadsadegh, F Essmann, A Tannapfel, E Gulbins, K Schulze-Osthoff, U R Hengge

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.2field-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

33 citing papers in PubMed, 63 citations in OpenAlex.

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  19. Regulation of Noxa-mediated apoptosis in Helicobacter pylori-infected gastric epithelial cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

M HassanDepartment of Dermatology, Heinrich-Heine-University, Duesseldorf, Germany.
A Alaoui
O Feyen
A Mirmohammadsadegh
F Essmann
A Tannapfel
E Gulbins
K Schulze-Osthoff
U R Hengge
Heinrich Heine University Düsseldorf · DEUniversity of Duisburg-Essen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular causes for resistance of melanoma to apoptosis are currently only partly understood. In the present study, we examined gene transfer and expression of the proapoptotic BH3-only protein Noxa as an alternative approach to chemotherapy and investigated the molecular mechanisms regulating Noxa-induced apoptosis. Noxa gene transfer caused dysregulation of both mitochondria and, as shown for the first time, also the endoplasmic reticulum, resulting in the accumulation of reactive oxygen species. Interestingly, expression of Noxa not only triggered the classical mitochondrial caspase cascade, but also resulted in the activation of apoptosis signal-regulating kinase1 and its downstream effectors c-Jun N-terminal kinase and p38. The activation of these kinases was abolished by antioxidants. Moreover, inhibition of the kinases by RNA interference or pharmacological inhibitors significantly attenuated Noxa-induced apoptosis. Thus, our data provide evidence for the involvement of multiple pathways in Noxa-induced apoptosis that are triggered at mitochondria and the endoplasmic reticulum, and suggest Noxa gene transfer as a complementary approach to chemotherapy.

Indexed as

ApoptosisMAP Kinase Signaling SystemAntioxidantsBH3 Interacting Domain Death Agonist ProteinCaspasesCell Line, TumorEndoplasmic ReticulumGene Transfer TechniquesHumansJNK Mitogen-Activated Protein KinasesMAP Kinase Kinase Kinase 5MelanomaMitochondriap38 Mitogen-Activated Protein KinasesProto-Oncogene Proteins c-bcl-2RNA InterferenceAntioxidantsBH3 Interacting Domain Death Agonist ProteinBID protein, humanCaspasesJNK Mitogen-Activated Protein KinasesMAP Kinase Kinase Kinase 5p38 Mitogen-Activated Protein KinasesPMAIP1 protein, humanProto-Oncogene Proteins c-bcl-2

Identifiers

PMID18408751
OpenAlexW2017377008

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.