Evidence map›Paper›PMID 17435549›Full record

ArticleAnnals of surgery2007

Bile salts induce resistance to apoptosis through NF-kappaB-mediated XIAP expression.

Douglas J Turner, Samuel M Alaish, Tongtong Zou, Jaladanki N Rao, Jian-Ying Wang, Eric D Strauch

Open access · greenAbstract read
In one paragraph

Article in Annals of surgery, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Gut microbiota in colorectal cancer development and therapy.Nature reviews. Clinical oncology · 2023
    Review
  8. The role of bile acids in carcinogenesis.Cellular and molecular life sciences : CMLS · 2022
    Review
  9. Review
  10. Article
  11. Article
  12. Role of bile acids in colon carcinogenesis.World journal of clinical cases · 2018
    Review
  13. The apoptotic effects ofDrug design, development and therapy · 2018
    Article
  14. Article
  15. Article
  16. A purine scaffold HSP90 inhibitor BIIB021 has selective activity against KSHV-associated primary effusion lymphoma and blocks vFLIP K13-induced NF-κB.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Article
  17. Review
  18. Article
  19. Article
  20. Effect of bile duct ligation on bile acid composition in mouse serum and liver.Liver international : official journal of the International Association for the Study of the Liver · 2012
    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 3 institutions in 1 country.

Douglas J TurnerDepartments of Surgery, University of Maryland School of Medicine, Baltimore, MD, USA. DTURNER@smail.umaryland.edu
Samuel M Alaish
Tongtong Zou
Jaladanki N Rao
Jian-Ying Wang
Eric D Strauch
University of Maryland, Baltimore · USVeterans Health Administration · USBaltimore VA Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apoptosis plays a critical role in intestinal mucosal homeostasis. We previously showed that the bile salt taurodeoxycholate has a beneficial effect on the intestinal mucosa through an increase in resistance to apoptosis mediated by nuclear factor (NF)-kappaB. The current study further characterizes the effect of bile salts on intestinal epithelial cell susceptibility to apoptosis and determines if the X-linked inhibitor of apoptosis protein (XIAP) regulates bile salt-induced resistance to apoptosis. Exposure of normal intestinal epithelial cells (IEC-6) to the conjugated bile salts taurodeoxycholate (TDCA) and taurochenodeoxycholate (TCDCA) resulted in an increase in resistance to tumor necrosis factor (TNF)-alpha and cycloheximide (CHX)-induced apoptosis, and NF-kappaB activation. Treatment with TDCA and TCDCA resulted in an increase in XIAP expression. Specific inhibition of NF-kappaB by infection with an adenoviral vector that expresses the IkappaBalpha super-repressor (IkappaBSR) prevented the induction of XIAP expression and the bile salt-mediated resistance to apoptosis. Treatment with the specific XIAP inhibitor Smac also overcame this increase in enterocyte resistance to apoptosis. Bile salts inhibited formation of the active caspase-3 from its precursor procaspase-3. Smac prevented the inhibitory effect of bile salts on caspase-3 activation. These results indicate that bile salts increase intestinal epithelial cell resistance to apoptosis through NF-kappaB-mediated XIAP expression. Bile salt-induced XIAP mediates resistance to TNF-alpha/CHX-induced apoptosis, at least partially, through inhibition of caspase-3 activity. These data support an important beneficial role of bile salts in regulation of mucosal integrity. Decreased enterocyte exposure to luminal bile salts, as occurs during starvation and parenteral nutrition, may have a detrimental effect on mucosal integrity.

Indexed as

Electrophoretic Mobility Shift AssayAnimalsApoptosisApoptosis Regulatory ProteinsBile Acids and SaltsCarrier ProteinsCaspase 3Cells, CulturedCycloheximideMitochondrial ProteinsNF-kappa BProtein Synthesis InhibitorsRatsX-Linked Inhibitor of Apoptosis ProteinApoptosis Regulatory ProteinsBile Acids and SaltsCarrier ProteinsCaspase 3CycloheximideDIABLO protein, ratMitochondrial ProteinsNF-kappa BProtein Synthesis InhibitorsX-Linked Inhibitor of Apoptosis Protein

Identifiers

PMID17435549
PMCPMC1877019
OpenAlexW2050228005

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.