Evidence map›Paper›PMID 12879007›Full record

ArticleOncogene2003

TID1, a mammalian homologue of the drosophila tumor suppressor lethal(2) tumorous imaginal discs, regulates activation-induced cell death in Th2 cells.

Josh Syken, Fernando Macian, Suneet Agarwal, Anjana Rao, Karl Münger

Abstract read
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In one paragraph

Article in Oncogene, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

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  10. Multi-faceted role of HSP40 in cancer.Clinical & experimental metastasis · 2009
    Review
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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

5 authors at 2 institutions in 1 country.

Josh SykenDepartment of Pathology, Harvard Medical School, 200 Longwood Avenue, D2/544A, Boston, MA 02115-5701, USA.
Fernando Macian
Suneet Agarwal
Anjana Rao
Karl Münger
Harvard University · USDana-Farber/Boston Children's Cancer and Blood Disorders Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously described two human DnaJ proteins, hTid-1L and hTid-1S, which are derived from alternative splicing of the TID1 gene, the human homologue of the Drosophila tumor suppressor lethal(2) tumorous imaginal discs, and showed that hTid-1L promoted while hTid-1S antagonized apoptosis. There are two subsets of helper T cells, Th1 and Th2, of which Th2 cells are significantly less prone to apoptosis induced by stimulation through the T-cell receptor. This apoptotic process is known as activation-induced cell death (AICD). The molecular basis for the differential susceptibility of Th1 and Th2 cells to AICD is not known. Here we show that the antiapoptotic variant, Tid-1S, is selectively induced in murine Th2 cells following activation. Expression of a dominant-negative mutant of hTid-1S in a Th2 cell line strikingly enhanced activation of caspase 3 in response to CD3 stimulation, and caused the cells to become sensitive to AICD. Hence, the accumulation of Tid-1S in Th2 cells following activation represents a novel mechanism that may contribute to the induction of apoptosis resistance during the activation of Th2 cells.

Indexed as

Amino Acid SequenceAnimalsApoptosisCaspase 3CaspasesCell DeathCell DifferentiationCell LineElectrophoresis, Polyacrylamide GelGenes, DominantHeat-Shock ProteinsHSP40 Heat-Shock ProteinsHumansJurkat CellsMiceMolecular Sequence DataCASP3 protein, humanCasp3 protein, mouseCaspase 3CaspasesDNAJA3 protein, humanDnaja3 protein, mouseHeat-Shock ProteinsHSP40 Heat-Shock Proteins

Identifiers

PMID12879007
OpenAlexW2169901433

What OpenQuestion holds

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Read underepoch 390

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.