Evidence map›Paper›PMID 13679856›Full record

ArticleOncogene2003

ARK5 suppresses the cell death induced by nutrient starvation and death receptors via inhibition of caspase 8 activation, but not by chemotherapeutic agents or UV irradiation.

Atsushi Suzuki, Gen-Ichi Kusakai, Atsuhiro Kishimoto, Jie Lu, Tsutomu Ogura, Hiroyasu Esumi

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

40 citing papers in PubMed, 96 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. MicroRNA-96: A therapeutic and diagnostic tumor marker.Iranian journal of basic medical sciences · 2022
    Review
  5. Role of ARK5 in cancer and other diseases (Review).Experimental and therapeutic medicine · 2021
    Review
  6. HIF-1α Metabolic Pathways in Human Cancer.Advances in experimental medicine and biology · 2021
    Review
  7. Article
  8. Article
  9. Expression level of NUAK1 in human nasopharyngeal carcinoma and its prognostic significance.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2018
    Article
  10. Article
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  12. Article
  13. Article
  14. Article
  15. Maternal Embryonic Leucine Zipper Kinase (MELK) as a Novel Mediator and Biomarker of Radioresistance in Human Breast Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Overexpression of ARK5 is associated with poor prognosis in hepatocellular carcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Article
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

6 authors at 1 institution in 1 country.

Atsushi SuzukiNational Cancer Center Research Institute East, Investigative Treatment Division, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577, Japan.
Gen-Ichi Kusakai
Atsuhiro Kishimoto
Jie Lu
Tsutomu Ogura
Hiroyasu Esumi
National Cancer Center Hospital East · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AMPK is a serine/threonine protein kinase family and we recently identified a novel member, ARK5. The activation of ARK5 is triggered by Akt, and ARK5 induces tumor cell survival during nutrient starvation. In the current study, we investigated the mechanisms of induction of cell survival by ARK5. Human hepatoma HepG2 cells undergo necrotic cell death within 24 h after the start of glucose starvation, and the cell death signaling has been found to be mediated by death-receptor-independent activation of caspase 8. When HepG2 cells were transfected with ARK5 expression vector and subjected to several cell death stimuli, ARK5 was found to suppress cell death by glucose starvation, TRAIL, and TNF-alpha, but not by ultraviolet irradiation, camptothecin, or doxorubicin. Western blotting analysis revealed that both TRAIL and glucose starvation induced Bid cleavage and FLIP degradation following caspase 8 activation in a time-dependent manner, and ARK5 overexpression clearly delayed Bid cleavage, FLIP degradation, and caspase 8 activation. On the basis of the results of this study, we report that cell survival induced by ARK5 is, at least in part, due to inhibition of caspase 8 activation.

Indexed as

Caspase InhibitorsIntracellular Signaling Peptides and ProteinsUltraviolet RaysAntineoplastic AgentsApoptosisApoptosis Regulatory ProteinsBH3 Interacting Domain Death Agonist ProteinCarcinoma, HepatocellularCarrier ProteinsCASP8 and FADD-Like Apoptosis Regulating ProteinCell SurvivalEnzyme ActivationGlucoseHumansLigandsLiver NeoplasmsAntineoplastic AgentsApoptosis Regulatory ProteinsBH3 Interacting Domain Death Agonist ProteinBID protein, humanCarrier ProteinsCASP8 and FADD-Like Apoptosis Regulating ProteinCaspase InhibitorsCFLAR protein, humanGlucoseIntracellular Signaling Peptides and ProteinsLigandsMembrane GlycoproteinsNUAK1 protein, humanProtein KinasesReceptors, Tumor Necrosis FactorRepressor ProteinsTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID13679856
OpenAlexW2090267559

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.