Evidence map›Paper›PMID 15100416›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2004

Suppression of tumor growth and cell proliferation by p13II, a mitochondrial protein of human T cell leukemia virus type 1.

Micol Silic-Benussi, Ilaria Cavallari, Tatiana Zorzan, Elisabetta Rossi, Hajime Hiraragi, Antonio Rosato, Kyoji Horie, Daniela Saggioro, Michael D Lairmore, Luc Willems and 3 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.4field-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

35 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
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  3. Article
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  5. Review
  6. Review
  7. Review
  8. Article
  9. Cell cycle regulation during viral infection.Methods in molecular biology (Clifton, N.J.) · 2014
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Mitochondria and viruses.Mitochondrion · 2011
    Review
  20. 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

13 authors at 3 institutions in 1 country.

Micol Silic-BenussiDepartment of Oncology and Surgical Sciences, University of Padua, Via Gattamelata 64, 35128 Padua, Italy.
Ilaria Cavallari
Tatiana Zorzan
Elisabetta Rossi
Hajime Hiraragi
Antonio Rosato
Kyoji Horie
Daniela Saggioro
Michael D Lairmore
Luc Willems
Luigi Chieco-Bianchi
Donna M D'Agostino
Vincenzo Ciminale
University of Padua · ITAzienda Ospedaliera di Padova · ITIstituto Oncologico Veneto · IT

Funding

Studies of p30 II and p13 II in HTLV-1 InfectionR03TW005705 · FIC · OHIO STATE UNIVERSITY · PI LAIRMORE, MICHAEL D · 2002 to 2004
$121k
FIC NIH HHS R03 TW005705FIC NIH HHS R03TW005705
6 · The paper itself

Abstract

Human T cell leukemia virus type 1 encodes an "accessory" protein named p13(II) that is targeted to mitochondria and triggers a rapid flux of K(+) and Ca(2+) across the inner membrane. In this study, we investigated the effects of p13(II) on tumorigenicity in vivo and on cell growth in vitro. Results showed that p13(II) significantly reduced the incidence and growth rate of tumors arising from c-myc and Ha-ras-cotransfected rat embryo fibroblasts. Consistent with these findings, HeLa-derived cell lines stably expressing p13(II) exhibited markedly reduced tumorigenicity, as well as reduced proliferation at high density in vitro. Mixed culture assays revealed that the phenotype of the p13(II) cell lines was dominant over that of control lines and was mediated by a heat-labile soluble factor. The p13(II) cell lines exhibited an enhanced response to Ca(2+)-mediated stimuli, as measured by increased sensitivity to C2-ceramide-induced apoptosis and by cAMP-responsive element-binding protein (CREB) phosphorylation in response to histamine. p13(II)-expressing Jurkat T cells also exhibited reduced proliferation, suggesting that the protein might exert similar effects in T cells, the primary target of HTLV-1 infection. These findings provide clues into the function of p13(II) as a negative regulator of cell growth and underscore a link between mitochondria, Ca(2+) signaling, and tumorigenicity.

Indexed as

Base SequenceBlotting, WesternCell CycleCell DivisionDNA PrimersFluorescent Antibody TechniqueHeLa CellsHumansHuman T-lymphotropic virus 1Jurkat CellsMitochondriaRetroviridae ProteinsDNA PrimersRetroviridae Proteinsrof protein, Human T-lymphotropic virus 1

Identifiers

PMID15100416
PMCPMC404096
OpenAlexW2098446992

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.