Evidence map›Paper›PMID 19184418›Full record

ArticleGlycoconjugate journal2009

Post-translational and transcriptional regulation of glycolipid glycosyltransferase genes in apoptotic breast carcinoma cells: VII. Studied by DNA-microarray after treatment with L-PPMP.

Rui Ma, N Matthew Decker, Vesta Anilus, Joseph R Moskal, Joseph Burgdorf, James R Johnson, Manju Basu, Sipra Banerjee, Subhash Basu

Abstract read
PubMed Publisher
In one paragraph

Article in Glycoconjugate journal, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. 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

9 authors at 3 institutions in 1 country.

Rui MaDepartment of Chemistry and Biochemistry, The University of Notre Dame, Notre Dame, IN 46556, USA.
N Matthew Decker
Vesta Anilus
Joseph R Moskal
Joseph Burgdorf
James R Johnson
Manju Basu
Sipra Banerjee
Subhash Basu
University of Notre Dame · USNorthwestern University · USCleveland Clinic · US

Funding

GLYCOLIPID METABOLISM IN TUMOR AND TRANSFORMED CELLSR01CA014764 · NCI · UNIVERSITY OF NOTRE DAME · PI BASU, SUBHASH C · 1985 to 1990
–
NCI NIH HHS CA-14764NINDS NIH HHS NS-18005
6 · The paper itself

Abstract

Functions of glycosphingolipids on the eukaryotic cell membranes during the onset of oncogenic processes and cell death are not well understood. Inhibitors of glycosphingolipid biosynthesis were recently found to trigger apoptosis in many carcinoma including breast cancer SKBR-3, MCF-7, and MDA-468 cells through either intrinsic or extrinsic apoptotic pathways as we previously reported. These anti-cancer inhibitors could increase ceramide concentration by blocking functions of glycolipid glycosyltransferases (GLTs). In this study, using a novel fluorescent dye (ASK-0) revealed the damage of cell organelle membranes by an inhibitor of glucosylceramide biosynthesis (L-PPMP). A highly drug- and cell-dependent regulation of MAPKs was also found by cis-platin and L-PPMP when inducing apoptosis in SKBR-3, MCF-7, and MDA-468 cells. A dose and time-dependent regulation of GLTs were investigated by enzymatic assay and DNA microarray analyses. These GLTs are involved in biosynthesis of Le(X) and sialosyl-Le(X) (neolactosyl-ceramide series) such as GalT-4 (UDP-Gal: LcOse3cer beta-galactosyltransferase, GalT-5 (UDP-Gal: nLcOse4Cer alpha1, 3galactosyltransferase, FucT-3 (GDP-Fucose: LM1 alpha1, 4fucosyltransferase). A similar effect was observed with the GLTs involved in the biosyntheses of Gg-series gangliosides, such as SAT-4 (CMP-NeuAc: GgOse4Cer alpha2, 3sialyltransferase, and SAT-2 (CMP-NeuAc: GM3 alpha2, 8sialyltransferase). The glycol-related gene DNA-microarrays also suggested the transcriptional regulation of several GLTs involved in the biosynthesis of neolactosylceramide containing cell-surface antigens in these apoptotic breast carcinoma cells. In the early apoptotic stages (2 to 6 h after L-PPMP treatment) in addition to GlcT-1 gene, several genes (betaGalTs and betaGlcNAcTs) in the SA-Le(a) pathway were stimulated.

Indexed as

Antineoplastic AgentsApoptosisCell Line, TumorCisplatinFucosyltransferasesGalactosyltransferasesGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticGlycosyltransferasesHumansModels, BiologicalMorpholinesOligonucleotide Array Sequence Analysis3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferaseAntineoplastic AgentsCisplatinFucosyltransferasesGalactosyltransferasesGlycosyltransferasesMorpholinestriaosylceramide 1,4-galactosyltransferase

Identifiers

PMID19184418
OpenAlexW2168458938

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.