Evidence map›Paper›PMID 30206308›Full record

ArticleLeukemia2019

Downregulating Notch counteracts Kras

Guangyao Kong, Xiaona You, Zhi Wen, Yuan-I Chang, Shuiming Qian, Erik A Ranheim, Christopher Letson, Xinmin Zhang, Yun Zhou, Yangang Liu and 11 more

Open access · greenAbstract read
In one paragraph

Article in Leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 17 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

21 authors at 6 institutions in 3 countries.

Guangyao Kong *National Local Joint Engineering Research Center of Biodiagnostics and Biotherapy, The Second Affiliated Hospital of Xian Jiaotong University, Xian, China. konggy@xjtu.edu.cn.
Xiaona You *McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.
Zhi WenMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.
Yuan-I ChangMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.
Shuiming QianWisconsin Institute for Discovery and Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI, USA.
Erik A RanheimDepartment of Pathology & Laboratory Medicine, University of Wisconsin School of Medicine and Public Health, University of Wisconsin Carbone Cancer Center, Madison, WI, USA.
Christopher LetsonMalignant Hematology, Moffitt Cancer Center, Tampa, FL, USA.
Xinmin ZhangBioInfoRx, Inc, Madison, WI, USA.
Yun ZhouMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.
Yangang LiuMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.
Adhithi RajagopalanCellular and Molecular Biology Program, University of Wisconsin-Madison, Madison, WI, USA.
Jingfang ZhangMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA.
Elliot StieglitzDepartment of Pediatrics, Benioff Children's Hospital, University of California-San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-7032-4623
Mignon LohDepartment of Pediatrics, Benioff Children's Hospital, University of California-San Francisco, San Francisco, CA, USA.
Inga HofmannDepartment of Pediatrics, University of Wisconsin-Madison, Madison, WI, USA.
David YangDepartment of Pathology & Laboratory Medicine, University of Wisconsin School of Medicine and Public Health, University of Wisconsin Carbone Cancer Center, Madison, WI, USA.
Xuehua ZhongWisconsin Institute for Discovery and Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI, USA.ORCID http://orcid.org/0000-0002-2350-0046
Eric PadronMalignant Hematology, Moffitt Cancer Center, Tampa, FL, USA.
Lan ZhouDepartment of Pathology, Case Western Reserve University, Cleveland, OH, USA.
Warren S PearDepartment of Pathology and Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA, USA.
Jing ZhangMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI, USA. zhang@oncology.wisc.edu.
University of Wisconsin–Madison · USMoffitt Cancer Center · USUniversity of California, San Francisco · USUniversity of Wisconsin Carbone Cancer Center · USCancer Research Institute · USCase Western Reserve University · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Christian Capitini · 1985 to 2026
$142.6M
Research Training in Childhood CancerT32CA128583 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Eric Alejandro Sweet-Cordero · 2007 to 2026
$6.0M
The role of TCOF1 in germline predisposition to and in leukemic transformation of chronic myelomonocytic leukemiaR01CA152108 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Jing Zhang · 2011 to 2026
$5.4M
Targeting Notch2 in Hematopoietic Cell Therapy.R01HL103827 · NHLBI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI ZHOU, LAN · 2012 to 2022
$4.3M
Uncovering the epigenetic codes for genome integrity, developmental and environmental interaction.R35GM124806 · NIGMS · WASHINGTON UNIVERSITY · PI XUEHUA ZHONG · 2017 to 2026
$4.2M
Dose-dependent Activation of the MEK/ERK Pathway in HematopoiesisR01HL113066 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI ZHANG, JING · 2013 to 2016
$1.5M
National Natural Science Foundation of China (National Science Foundation of China) NO.81600100NCI NIH HHS P30 CA014520NCI NIH HHS R01 CA152108NCI NIH HHS T32 CA128583NHLBI NIH HHS R01 HL103827NHLBI NIH HHS R01 HL113066NIGMS NIH HHS R35 GM124806U.S. Department of Health & Human Services | National Institutes of Health (NIH) CA152108U.S. Department of Health & Human Services | National Institutes of Health (NIH) HL113066
6 · The paper itself

Abstract

The Notch signaling pathway contributes to the pathogenesis of a wide spectrum of human cancers, including hematopoietic malignancies. Its functions are highly dependent on the specific cellular context. Gain-of-function NOTCH1 mutations are prevalent in human T-cell leukemia, while loss of Notch signaling is reported in myeloid leukemias. Here, we report a novel oncogenic function of Notch signaling in oncogenic Kras-induced myeloproliferative neoplasm (MPN). We find that downregulation of Notch signaling in hematopoietic cells via DNMAML expression or Pofut1 deletion significantly blocks MPN development in Kras

Indexed as

AnimalsCell ProliferationCytokinesDown-RegulationDual Specificity Phosphatase 1Leukemia, MyeloidMAP Kinase Signaling SystemMiceMice, Inbred C57BLMitochondriaMutationMyeloproliferative DisordersOxidative PhosphorylationProto-Oncogene Proteins p21(ras)Receptors, NotchSignal TransductionCytokinesDual Specificity Phosphatase 1KRAS protein, humanProto-Oncogene Proteins p21(ras)Receptors, Notch

Identifiers

PMID30206308
PMCPMC6405304
OpenAlexW2891329755

What OpenQuestion holds

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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.