Evidence map›Paper›PMID 30643195›Full record

ArticleOncogene2019

ATDC mediates a TP63-regulated basal cancer invasive program.

Phillip L Palmbos, Yin Wang, Armand Bankhead Iii, Alan J Kelleher, Lidong Wang, Huibin Yang, McKenzie L Ahmet, Erica R Gumkowski, Samuel D Welling, Brian Magnuson and 8 more

Abstract read
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
10.4field-weighted citation impact, top 1% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

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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

18 authors at 2 institutions in 1 country.

Phillip L PalmbosDepartment of Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA. ppalmbos@med.umich.edu.
Yin WangDepartment of Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Armand Bankhead IiiRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Alan J KelleherDepartment of Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Lidong WangDepartment of Surgery, NYU Langone Health, New York, NY, 10016, USA.
Huibin YangDepartment of Radiation Oncology, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
McKenzie L AhmetDepartment of Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Erica R GumkowskiDepartment of Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Samuel D WellingRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Brian MagnusonRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Jacob LefleinRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Guadalupe Lorenzatti HilesRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.ORCID http://orcid.org/0000-0002-8423-3279
Ethan V AbelRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Michele L DziubinskiRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Sumithra UrsRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Mark L DayDepartment of Urology, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Mats E LjungmanRogel Cancer Center, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Diane M SimeoneDepartment of Surgery, NYU Langone Health, New York, NY, 10016, USA.
University of Michigan · USNYU Langone Health · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
Reagent/Service CoreP01CA165980 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WU, XUE-RU · 2013 to 2023
$13.5M
Oncogenic Function of ATDC in Bladder CancerR01CA174836 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SIMEONE, DIANE M · 2014 to 2018
$2.3M
Regulation of ATDC by TP63 and its role in bladder cancerK08CA201335 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PALMBOS, PHILLIP L · 2016 to 2020
$875k
NCATS NIH HHS UL1 TR002240NCI NIH HHS K08 CA201335NCI NIH HHS L30 CA171029NCI NIH HHS P01 CA165980NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA174836U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) CA17483601U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) CA201335
6 · The paper itself

Abstract

Basal subtype cancers are deadly malignancies but the molecular events driving tumor lethality are not completely understood. Ataxia-telangiectasia group D complementing gene (ATDC, also known as TRIM29), is highly expressed and drives tumor formation and invasion in human bladder cancers but the factor(s) regulating its expression in bladder cancer are unknown. Molecular subtyping of bladder cancer has identified an aggressive basal subtype, which shares molecular features of basal/squamous tumors arising in other organs and is defined by activation of a TP63-driven gene program. Here, we demonstrate that ATDC is linked with expression of TP63 and highly expressed in basal bladder cancers. We find that TP63 binds to transcriptional regulatory regions of ATDC and KRT14 directly, increasing their expression, and that ATDC and KRT14 execute a TP63-driven invasive program. In vivo, ATDC is required for TP63-induced bladder tumor invasion and metastasis. These results link TP63 and the basal gene expression program to ATDC and to aggressive tumor behavior. Defining ATDC as a molecular determinant of aggressive, basal cancers may lead to improved biomarkers and therapeutic approaches.

Indexed as

Cell Line, TumorDNA-Binding ProteinsGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessNeoplasms, Basal CellNeoplasms, Squamous CellTranscription FactorsTranscription, GeneticTumor Suppressor ProteinsUrinary Bladder NeoplasmsDNA-Binding ProteinsTP63 protein, humanTranscription FactorsTRIM29 protein, humanTumor Suppressor Proteins

Identifiers

PMID30643195
PMCPMC6499660
OpenAlexW2909745848

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.