Evidence map›Paper›PMID 23600753›Full record

ArticleCancer science2013

Adult T-cell leukemia cells are characterized by abnormalities of Helios expression that promote T cell growth.

Satomi Asanuma, Makoto Yamagishi, Katsuaki Kawanami, Kazumi Nakano, Aiko Sato-Otsubo, Satsuki Muto, Masashi Sanada, Tadanori Yamochi, Seiichiro Kobayashi, Atae Utsunomiya and 5 more

Open access · greenAbstract read
In one paragraph

Article in Cancer science, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

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  5. Clinical application of genomic aberrations in adult T-cell leukemia/lymphoma.Journal of clinical and experimental hematopathology : JCEH · 2020
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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

15 authors at 4 institutions in 1 country.

Satomi AsanumaGraduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan.
Makoto Yamagishi
Katsuaki Kawanami
Kazumi Nakano
Aiko Sato-Otsubo
Satsuki Muto
Masashi Sanada
Tadanori Yamochi
Seiichiro Kobayashi
Atae Utsunomiya
Masako Iwanaga
Kazunari Yamaguchi
Kaoru Uchimaru
Seishi Ogawa
Toshiki Watanabe
The University of Tokyo · JPImamura Hospital · JPNational Institute of Infectious Diseases · JPTeikyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular abnormalities involved in the multistep leukemogenesis of adult T-cell leukemia (ATL) remain to be clarified. Based on our integrated database, we focused on the expression patterns and levels of Ikaros family genes, Ikaros, Helios, and Aiolos, in ATL patients and HTLV-1 carriers. The results revealed profound deregulation of Helios expression, a pivotal regulator in the control of T-cell differentiation and activation. The majority of ATL samples (32/37 cases) showed abnormal splicing of Helios expression, and four cases did not express Helios. In addition, novel genomic loss in Helios locus was observed in 17/168 cases. We identified four ATL-specific short Helios isoforms and revealed their dominant-negative function. Ectopic expression of ATL-type Helios isoform as well as knockdown of normal Helios or Ikaros promoted T-cell growth. Global mRNA profiling and pathway analysis showed activation of several signaling pathways important for lymphocyte proliferation and survival. These data provide new insights into the molecular involvement of Helios function in the leukemogenesis and phenotype of ATL cells, indicating that Helios deregulation is one of the novel molecular hallmarks of ATL.

Indexed as

Cell Growth ProcessesCell LineCell Line, TumorCytoplasmExonsHEK293 CellsHeLa CellsHumansHuman T-lymphotropic virus 1Ikaros Transcription FactorLeukemia-Lymphoma, Adult T-CellProtein IsoformsSignal TransductionT-LymphocytesIkaros Transcription FactorIKZF2 protein, humanIKZF3 protein, humanProtein Isoforms

Identifiers

PMID23600753
PMCPMC7657222
OpenAlexW2094630349

What OpenQuestion holds

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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.