Evidence map›Paper›PMID 22785201›Full record

ArticleCancer biology & therapy2012

HuR's post-transcriptional regulation of Death Receptor 5 in pancreatic cancer cells.

Danielle M Pineda, David W Rittenhouse, Christopher C Valley, Joseph A Cozzitorto, Richard A Burkhart, Benjamin Leiby, Jordan M Winter, Matthew C Weber, Eric R Londin, Isidore Rigoutsos and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

31 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  11. Article
  12. Complex HuR function in pancreatic cancer cells.Wiley interdisciplinary reviews. RNA · 2018
    Review
  13. Article
  14. Posttranscriptional Regulation ofCancer research · 2017
    Article
  15. Article
  16. Article
  17. Review
  18. Hallmarks of cancer and AU-rich elements.Wiley interdisciplinary reviews. RNA · 2017
    Review
  19. Article
  20. 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

15 authors at 7 institutions in 1 country.

Danielle M PinedaDepartment of Surgery, Division of Surgical Research, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA, USA.
David W Rittenhouse
Christopher C Valley
Joseph A Cozzitorto
Richard A Burkhart
Benjamin Leiby
Jordan M Winter
Matthew C Weber
Eric R Londin
Isidore Rigoutsos
Charles J Yeo
Myriam Gorospe
Agnieska K Witkiewicz
Jonathan N Sachs
Jonathan R Brody
Jefferson College · USThomas Jefferson University · USPhiladelphia University · USInstitute on Aging · USNational Institute on Aging · USUniversity of Minnesota · USUniversity of Minnesota System · US

Funding

Post-transcriptional Regulation Of Proliferative and Stress Response GenesZIAAG000511 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$25.4M
Influence of Post-transcriptional Gene Regulation on Cell Senescence and AgingZIAAG000393 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$24.1M
6 · The paper itself

Abstract

Apoptosis is one of the core signaling pathways disrupted in pancreatic ductal adenocarcinoma (PDA). Death receptor 5 (DR5) is a member of the tumor necrosis factor (TNF)-receptor superfamily that is expressed in cancer cells. Binding of TNF-related apoptosis-inducing ligand (TRAIL) to DR5 is a potent trigger of the extrinsic apoptotic pathway, and numerous clinical trials are based on DR5-targeted therapies for cancer, including PDA. Human antigen R (HuR), an RNA-binding protein, regulates a select number of transcripts under stress conditions. Here we report that HuR translocates from the nucleus to the cytoplasm of PDA cells upon treatment with a DR5 agonist. High doses of DR5 agonist induce cleavage of both HuR and caspase 8. HuR binds to DR5 mRNA at the 5'-untranslated region (UTR) in PDA cells in response to different cancer-associated stressors and subsequently represses DR5 protein expression; silencing HuR augments DR5 protein production by enabling its translation and thus enhances apoptosis. In PDA specimens (n = 53), negative HuR cytoplasmic expression correlated with elevated DR5 expression (odds ratio 16.1, p < 0.0001). Together, these data demonstrate a feedback mechanism elicited by HuR-mediated repression of the key apoptotic membrane protein DR5.

Indexed as

RNA Processing, Post-Transcriptional5' Untranslated RegionsAntimetabolites, AntineoplasticCell Line, TumorCytoplasmDeoxycytidineELAV ProteinsGemcitabineGene Expression Regulation, NeoplasticGene SilencingHumansPancreatic NeoplasmsProtein TransportProteolysisReceptors, TNF-Related Apoptosis-Inducing LigandRNA, Messenger5' Untranslated RegionsAntimetabolites, AntineoplasticDeoxycytidineELAV ProteinsGemcitabineReceptors, TNF-Related Apoptosis-Inducing LigandRNA, Messenger

Identifiers

PMID22785201
PMCPMC3414415
OpenAlexW2039644505

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.