Evidence map›Paper›PMID 12138191›Full record

ArticleMolecular and cellular biology2002

Human papillomavirus oncoprotein E6 inactivates the transcriptional coactivator human ADA3.

Ajay Kumar, Yongtong Zhao, Gaoyuan Meng, Musheng Zeng, Seetha Srinivasan, Laurie M Delmolino, Qingshen Gao, Goberdhan Dimri, Georg F Weber, David E Wazer and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

59 citing papers in PubMed, 144 citations in OpenAlex.

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  20. Human papillomavirus oncoproteins and apoptosis (Review).Experimental and therapeutic medicine · 2014
    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

12 authors at 2 institutions in 1 country.

Ajay KumarDivision of Radiation and Cancer Biology, Department of Radiation Oncology, New England Medical Center, Boston, Massachusetts 02111, USA.
Yongtong Zhao
Gaoyuan Meng
Musheng Zeng
Seetha Srinivasan
Laurie M Delmolino
Qingshen Gao
Goberdhan Dimri
Georg F Weber
David E Wazer
Hamid Band
Vimla Band
Tufts University · USBrigham and Women's Hospital · US

Funding

TYROSINE KINASE REGULATION VIA PROTEIN DEGRADATIONR01CA087986 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, HAMID · 2000 to 2015
$4.2M
THE ROLE OF A NOVEL GAP IN EPITHELIAL ONCOGENESISR01CA081076 · NCI · TUFTS MEDICAL CENTER · PI BAND, VIMLA · 1999 to 2003
$988k
FUNCTIONAL DISSECTION OF CBLS TRANSFORMING DOMAINR01CA076118 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI BAND, HAMID · 1998 to 2002
$713k
HUMAN MAMMARY EPITHELIAL CELL IMMORTALIZATIONR01CA070195 · NCI · TUFTS MEDICAL CENTER · PI BAND, VIMLA · 1998 to 2002
$706k
REGULATING TYROSINE KINASE SIGNALS IN BREAST CANCERR01CA075075 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI BAND, HAMID · 1997 to 2001
$508k
NCI NIH HHS CA70195NCI NIH HHS CA75075NCI NIH HHS CA76118NCI NIH HHS CA81076NCI NIH HHS CA87986NCI NIH HHS R01 CA081076NCI NIH HHS R01 CA087986
6 · The paper itself

Abstract

High-risk human papillomaviruses (HPVs) are associated with carcinomas of the cervix and other genital tumors. The HPV oncoprotein E6 is essential for oncogenic transformation. We identify here hADA3, human homologue of the yeast transcriptional coactivator yADA3, as a novel E6-interacting protein and a target of E6-induced degradation. hADA3 binds selectively to the high-risk HPV E6 proteins and only to immortalization-competent E6 mutants. hADA3 functions as a coactivator for p53-mediated transactivation by stabilizing p53 protein. Notably, three immortalizing E6 mutants that do not induce direct p53 degradation but do interact with hADA3 induced the abrogation of p53-mediated transactivation and G(1) cell cycle arrest after DNA damage, comparable to wild-type E6. These findings reveal a novel strategy of HPV E6-induced loss of p53 function that is independent of direct p53 degradation. Given the likely role of the evolutionarily conserved hADA3 in multiple coactivator complexes, inactivation of its function may allow E6 to perturb numerous cellular pathways during HPV oncogenesis.

Indexed as

Antineoplastic AgentsCell CycleCell LineCell Transformation, NeoplasticDoxorubicinGenes, ReporterHumansOncogene Proteins, ViralPapillomaviridaeProtein BindingRecombinant Fusion ProteinsRepressor ProteinsTissue DistributionTranscriptional ActivationTranscription FactorsTranscription, GeneticAntineoplastic AgentsDoxorubicinE6 protein, Human papillomavirus type 16Oncogene Proteins, ViralRecombinant Fusion ProteinsRepressor ProteinsTADA3 protein, humanTranscription FactorsTumor Suppressor Protein p53

Identifiers

PMID12138191
PMCPMC133989
OpenAlexW2117316674

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.