Evidence map›Paper›PMID 17557191›Full record

ArticleMolecular and cellular biochemistry2007

Two specific inhibitors of the phosphatidylinositol 3-kinase LY294002 and wortmannin up-regulate beta1,4-galactosyltransferase I and thus sensitize SMMC-7721 human hepatocarcinoma cells to cycloheximide-induced apoptosis.

Jialin Shen, Jianhai Jiang, Yuanyan Wei, Lei Zhou, Dan Liu, Jin Zhou, Jianxin Gu

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Article in Molecular and cellular biochemistry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

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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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Human cholangiocarcinoma development is associated with dysregulation of opioidergic modulation of cholangiocyte growth.Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver · 2009
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4 · The record

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5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Jialin ShenGene Research Center, Shanghai Medical College of Fudan University, Shanghai 200032, P. R. China.
Jianhai Jiang
Yuanyan Wei
Lei Zhou
Dan Liu
Jin Zhou
Jianxin Gu
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous study indicated that beta1,4-galactosyltransferase I (beta1,4GT1) was up-regulated by cycloheximide (CHX) and thus enhanced apoptosis induced by CHX in SMMC-7721 cells. In this study, we reported that constitutively active Akt protein (myr-Akt) inhibited CHX-induced apoptosis in SMMC-7721 cells through down-regulating beta1,4GT1. However, the two PI3K inhibitors LY294002 and wortmannin treatment up-regulated beta1,4GT1 through enhancing Sp1 protein expression and consequently increased CHX-induced SMMC-7721 cells apoptosis. Besides, our results suggested that beta1,4GT1 and cell surface galactose residues synthesized by elevated beta1,4GT1 played an important role in SMMC-7721 cells apoptosis treated with CHX and PI3K inhibitor together. Moreover, we found that CHX accentuated beta1,4GT1 through down-regulating Akt expression to mediate SMMC-7721 cells apoptosis. Taken together, PI3K inhibitors LY294002 and wortmannin up-regulated beta1,4GT1 and enhanced CHX-induced apoptosis in SMMC-7721 cells, which suggested that PI3K inhibitors might have therapeutic potential when combined with CHX in the treatment of hepatoma.

Indexed as

AndrostadienesAntineoplastic Combined Chemotherapy ProtocolsApoptosisCarcinoma, HepatocellularCell Line, TumorChromonesCycloheximideDrug Evaluation, PreclinicalDrug SynergismGalactosyltransferasesGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHumansLiver NeoplasmsMorpholinesPhosphatidylinositol 3-Kinases2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneAndrostadienesbeta1,4-galactosyltransferase, humanChromonesCycloheximideGalactosyltransferasesMorpholinesPhosphatidylinositol 3-KinasesWortmannin

Identifiers

PMID17557191
OpenAlexW2049090298

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Registered trials

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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.