Evidence map›Paper›PMID 19740745›Full record

ArticleThe Journal of biological chemistry2009

A truncated form of p23 down-regulates telomerase activity via disruption of Hsp90 function.

Sang Hyeok Woo, Sungkwan An, Hyung-Chahn Lee, Hyeon-Ok Jin, Sung-Keum Seo, Doo-Hyun Yoo, Kee-Ho Lee, Chang Hun Rhee, Eui-Ju Choi, Seok-Il Hong and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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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

11 authors at 3 institutions in 1 country.

Sang Hyeok WooDivision of Radiation Cancer Research, Korea Institute of Radiological & Medical Sciences, Nowon-gu, Seoul 139-706, Korea.
Sungkwan An
Hyung-Chahn Lee
Hyeon-Ok Jin
Sung-Keum Seo
Doo-Hyun Yoo
Kee-Ho Lee
Chang Hun Rhee
Eui-Ju Choi
Seok-Il Hong
In-Chul Park
Korea Institute of Radiological and Medical Sciences · KRKonkuk University · KRKorea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Hsp90-associated protein p23 modulates Hsp90 activity during the final stages of the chaperone pathway to facilitate maturation of client proteins. Previous reports indicate that p23 cleavage induced by caspases during cell death triggers destabilization of client proteins. However, the specific role of truncated p23 (Delta p23) in this process and the underlying mechanisms remain to be determined. One such client protein, hTERT, is a telomerase catalytic subunit regulated by several chaperone proteins, including Hsp90 and p23. In the present study, we examined the effects of p23 cleavage on hTERT stability and telomerase activity. Our data showed that overexpression of Delta p23 resulted in a decrease in hTERT levels, and a down-regulation in telomerase activity. Serine phosphorylation of Hsp90 was significantly reduced in cells expressing high levels of Delta p23 compared with those expressing full-length p23. Mutation analyses revealed that two serine residues (Ser-231 and Ser-263) in Hsp90 are important for activation of telomerase, and down-regulation of telomerase activity by Delta p23 was associated with inhibition of cell growth and sensitization of cells to cisplatin. Our data aid in determining the mechanism underlying the regulation of telomerase activity by the chaperone complex during caspase-dependent cell death.

Indexed as

Down-RegulationCell LineDNA-Binding ProteinsHSP90 Heat-Shock ProteinsHumansPhosphorylationProtein StabilityTelomeraseDNA-Binding ProteinsHSP90 Heat-Shock Proteinsprotein p23Telomerase

Identifiers

PMID19740745
PMCPMC2781486
OpenAlexW1985483310

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.