Evidence map›Paper›PMID 11494148›Full record

ArticleOncogene2001

STAT3 activation is required for Asp(816) mutant c-Kit induced tumorigenicity.

Z Q Ning, J Li, M McGuinness, R J Arceci

Abstract read
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In one paragraph

Article in Oncogene, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 80 citations in OpenAlex.

  1. A CanineAnimals : an open access journal from MDPI · 2025
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  7. Dasatinib inhibits the growth of molecularly heterogeneous myeloid leukemias.Clinical cancer research : an official journal of the American Association for Cancer Research · 2010
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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

4 authors at 1 institution in 1 country.

Z Q NingDivision of Hematology/Oncology, Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
J Li
M McGuinness
R J Arceci
Cincinnati Children's Hospital Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activating mutations of c-kit at codon 816 (Asp(816)) have been identified in variety of malignancies, including acute myeloid leukemia (AML), mastocytosis and germ cell tumors. The mutant c-Kit receptor confers cytokine independence and induces tumorigenicity. However, the molecular mechanisms, particularly the changes in the signal transduction pathways, responsible for these biological effects induced by mutant c-Kit are largely undefined. Using the human embryonic kidney cell line, 293, we show in the current report that constitutive activation of STAT3 and STAT1 is associated with D816H mutant c-Kit. Transfection of dominant negative STAT3, but not STAT1 inhibits mutant c-Kit mediated anchorage-independent growth in vitro and tumor formation in vivo. Expression of constitutively activated STAT3 restores the mutant c-Kit receptor's transforming ability in 293 cells. These results demonstrate that activation of STAT3 by Asp(816) mutant c-Kit is required for the anchorage-independent growth and tumorigenicity induced by Asp(816) mutant c-Kit.

Indexed as

OncogenesAmino Acid SubstitutionAnimalsCell DivisionCell Line, TransformedCells, CulturedCell Transformation, NeoplasticCodonDimerizationDNA-Binding ProteinsHumansKidneyMiceMice, Inbred NODMice, SCIDMutation, MissenseCodonDNA-Binding ProteinsProto-Oncogene Proteins c-kitRecombinant ProteinsSTAT1 protein, humanStat1 protein, mouseSTAT1 Transcription FactorSTAT3 protein, humanStat3 protein, mouseSTAT3 Transcription FactorStem Cell FactorTrans-Activators

Identifiers

PMID11494148
OpenAlexW2015581521

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.