Evidence map›Paper›PMID 29849118›Full record

ArticleOncogene2018

Maintenance and pharmacologic targeting of ROR1 protein levels via UHRF1 in t(1;19) pre-B-ALL.

Marilynn Chow, Lina Gao, Jason D MacManiman, Vincent T Bicocca, Bill H Chang, Joshi J Alumkal, Jeffrey W Tyner

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Epigenetics-targeted drugs: current paradigms and future challenges.Signal transduction and targeted therapy · 2024
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. 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

7 authors at 1 institution in 1 country.

Marilynn ChowDepartment of Cell, Developmental, and Cancer Biology, Oregon Health and Science University, Portland, USA.
Lina GaoKnight Cancer Institute, Oregon Health and Science University, Portland, USA.
Jason D MacManimanKnight Cancer Institute, Oregon Health and Science University, Portland, USA.
Vincent T BicoccaKnight Cancer Institute, Oregon Health and Science University, Portland, USA.
Bill H ChangKnight Cancer Institute, Oregon Health and Science University, Portland, USA.
Joshi J AlumkalKnight Cancer Institute, Oregon Health and Science University, Portland, USA.
Jeffrey W TynerDepartment of Cell, Developmental, and Cancer Biology, Oregon Health and Science University, Portland, USA. tynerj@ohsu.edu.
Oregon Health & Science University · US

Funding

ROR1 as a Therapeutic Target in Acute Lymphoblastic LeukemiaR00CA151457 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TYNER, JEFFREY WALLACE · 2012 to 2014
$723k
Oregon Clinical and Translational Research InstituteTL1TR000129 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI ELLISON, DAVID H · 2012 to 2015
$613k
ROR1 as a Therapeutic Target in Acute Lymphoblastic LeukemiaK99CA151457 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TYNER, JEFFREY WALLACE · 2010 to 2011
$256k
NCATS NIH HHS TL1 TR000129NCI NIH HHS K99 CA151457NCI NIH HHS R00 CA151457
6 · The paper itself

Abstract

Expression of the transmembrane pseudokinase ROR1 is required for survival of t(1;19)-pre-B-cell acute lymphoblastic leukemia (t(1;19) pre-B-ALL), chronic lymphocytic leukemia, and many solid tumors. However, targeting ROR1 with small-molecules has been challenging due to the absence of ROR1 kinase activity. To identify genes that regulate ROR1 expression and may, therefore, serve as surrogate drug targets, we employed an siRNA screening approach and determined that the epigenetic regulator and E3 ubiquitin ligase, UHRF1, is required for t(1;19) pre-B-ALL cell viability in a ROR1-dependent manner. Upon UHRF1 silencing, ROR1 protein is reduced without altering ROR1 mRNA, and ectopically expressed UHRF1 is sufficient to increase ROR1 levels. Additionally, proteasome inhibition rescues loss of ROR1 protein after UHRF1 silencing, suggesting a role for the proteasome in the UHRF1-ROR1 axis. Finally, we show that ROR1-positive cells are twice as sensitive to the UHRF1-targeting drug, naphthazarin, and undergo increased apoptosis compared to ROR1-negative cells. Naphthazarin elicits reduced expression of UHRF1 and ROR1, and combination of naphthazarin with inhibitors of pre-B cell receptor signaling results in further reduction of cell survival compared with either inhibitor alone. Therefore, our work reveals a mechanism by which UHRF1 stabilizes ROR1, suggesting a potential targeting strategy to inhibit ROR1 in t(1;19) pre-B-ALL and other malignancies.

Indexed as

Molecular Targeted TherapyCCAAT-Enhancer-Binding ProteinsCell Line, TumorCell SurvivalDown-RegulationGene Expression Regulation, NeoplasticGene SilencingHumansLeukemia, Lymphocytic, Chronic, B-CellNaphthoquinonesReceptor Tyrosine Kinase-like Orphan ReceptorsUbiquitin-Protein LigasesCCAAT-Enhancer-Binding ProteinsnaphthazarinNaphthoquinonesReceptor Tyrosine Kinase-like Orphan ReceptorsROR1 protein, humanUbiquitin-Protein LigasesUHRF1 protein, human

Identifiers

PMID29849118
PMCPMC6150818
OpenAlexW2805715756

What OpenQuestion holds

Textmetadata
LicenceTDM
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.