Evidence map›Paper›PMID 7935379›Full record

ArticleMolecular and cellular biology1994

Tissue transglutaminase and apoptosis: sense and antisense transfection studies with human neuroblastoma cells.

G Melino, M Annicchiarico-Petruzzelli, L Piredda, E Candi, V Gentile, P J Davies, M Piacentini

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In one paragraph

Article in Molecular and cellular biology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
14.4field-weighted citation impact, top 1% 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

52 citing papers in PubMed, 254 citations in OpenAlex.

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  9. Cyclin A1 expression and paclitaxel resistance in human ovarian cancer cells.European journal of cancer (Oxford, England : 1990) · 2016
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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

7 authors at 3 institutions in 1 country.

G MelinoDepartment of Experimental Medicine, University of Rome Tor Vergata, Italy.
M Annicchiarico-Petruzzelli
L Piredda
E Candi
V Gentile
P J Davies
M Piacentini
University of Rome Tor Vergata · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Naples Federico II · IT

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
HUMAN NEUROBLASTOMA CELL TRANSDIFFERENTIATIONR01CA041520 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI BIEDLER, JUNE L. · 1986 to 1993
–
NCI NIH HHS CA-08748NCI NIH HHS CA-41520
6 · The paper itself

Abstract

In this report, we show that the overexpression of tissue transglutaminase (tTG) in the human neuroblastoma cell line SK-N-BE(2) renders these neural crest-derived cells highly susceptible to death by apoptosis. Cells transfected with a full-length tTG cDNA, under the control of a constitutive promoter, show a drastic reduction in proliferative capacity paralleled by a large increase in cell death rate. The dying tTG-transfected cells exhibit both cytoplasmic and nuclear changes characteristic of cells undergoing apoptosis. The tTG-transfected cells express high Bcl-2 protein levels as well as phenotypic neural cell adhesion molecule markers (NCAM and neurofilaments) of cells differentiating along the neuronal pathway. In keeping with these findings, transfection of neuroblastoma cells with an expression vector containing segments of the human tTG cDNA in antisense orientation resulted in a pronounced decrease of both spontaneous and retinoic acid (RA)-induced apoptosis. We also present evidence that (i) the apoptotic program of these neuroectodermal cells is strictly regulated by RA and (ii) cell death by apoptosis in the human neuroblastoma SK-N-BE(2) cells preferentially occurs in the substrate-adherent phenotype. For the first time, we report here a direct effect of tTG in the phenotypic maturation toward apoptosis. These results indicate that the tTG-dependent irreversible cross-linking of intracellular protein represents an important biochemical event in the induction of the structural changes featuring cells dying by apoptosis.

Indexed as

ApoptosisCell Adhesion Molecules, NeuronalCloning, MolecularGene ExpressionGenetic VariationHumansNeural CrestNeuroblastomaProtein Processing, Post-TranslationalProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2Recombinant ProteinsRNA, AntisenseSelection, GeneticTranscription, GeneticTransfectionCell Adhesion Molecules, NeuronalProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2Recombinant ProteinsRNA, AntisenseTransglutaminasesTretinoin

Identifiers

PMID7935379
PMCPMC359188
OpenAlexW2102690359

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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.