Evidence map›Paper›PMID 12082531›Full record

ArticleOncogene2002

Reconstitution of hTERT restores tumorigenicity in melanoma-derived c-Myc low-expressing clones.

Annamaria Biroccio, Sarah Amodei, Barbara Benassi, Marco Scarsella, Anna Cianciulli, Marcella Mottolese, Donatella Del Bufalo, Carlo Leonetti, Gabriella Zupi

Abstract read
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In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 27 citations in OpenAlex.

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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

9 authors.

Annamaria BiroccioExperimental Chemotherapy Laboratory, Regina Elena Cancer Institute, Rome, Italy.
Sarah Amodei
Barbara Benassi
Marco Scarsella
Anna Cianciulli
Marcella Mottolese
Donatella Del Bufalo
Carlo Leonetti
Gabriella Zupi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

c-Myc is involved in the control of telomerase activity through its ability to induce the expression of the catalytic subunit of the enzyme, the human telomerase reverse transcriptase (hTERT). Our aim was to study whether telomerase plays a critical role in c-Myc-dependent tumorigenicity of melanoma cells. By using M14-derived clones, expressing low levels of c-Myc, we demonstrated that the down-regulation of c-Myc reduced cell proliferation rate, cloning efficiency and tumorigenicity and increased the apoptotic rate. Decreased tumorigenic potential correlated with reduced hTERT gene expression, telomerase activity and telomere shortening. Introduction of wild-type hTERT into these cells increased their proliferation rate and partially re-established their tumorigenic potential, at early passages, even though the apoptotic rate of the population remained unaltered. After several in vitro passages, hTERT-mediated cell proliferation made the tumorigenic potential of the c-Myc low-expressing clones comparable to that of the M14 parental line. Over-expression of the mutant biologically inactive hTERT did not drive cells to proliferate. In conclusion, our results demonstrate that the reconstitution of high levels of telomerase activity reverses the low tumorigenicity due to low c-Myc expression.

Indexed as

AnimalsApoptosisCell DivisionClone CellsDNA-Binding ProteinsGene Expression Regulation, NeoplasticGenes, mycHumansMelanomaMiceMice, NudeNeoplasm ProteinsNeoplasm TransplantationProto-Oncogene Proteins c-mycRecombinant Fusion ProteinsTelomeraseDNA-Binding ProteinsNeoplasm ProteinsProto-Oncogene Proteins c-mycRecombinant Fusion ProteinsTelomerase

Identifiers

PMID12082531
OpenAlexW2330907173

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.