Evidence map›Paper›PMID 20981007›Full record

Trial reportClinical pharmacology and therapeutics2010

Promoter polymorphisms in the β-2 adrenergic receptor are associated with drug-induced gene expression changes and response in acute lymphoblastic leukemia.

N Pottier, S W Paugh, C Ding, D Pei, W Yang, S Das, E H Cook, C-H Pui, M V Relling, M H Cheok and 1 more

Open access · greenAbstract readClinical Trial, Phase IIIComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology and therapeutics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. β-Adrenoceptors in Cancer: Old Players and New Perspectives.Handbook of experimental pharmacology · 2024
    Review
  2. Review
  3. Article
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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

11 authors at 5 institutions in 2 countries.

N PottierEA2679, Faculté de Médecine de Lille, Pôle Recherche, Lille, France.
S W Paugh
C Ding
D Pei
W Yang
S Das
E H Cook
C-H Pui
M V Relling
M H Cheok
W E Evans
St. Jude Children's Research Hospital · USAmerican Association of Colleges of Pharmacy · USInserm · FRUniversity of Chicago · USUniversity of Illinois Chicago · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Whole GenomeU01GM061393 · NIGMS · UNIVERSITY OF CHICAGO · PI DOLAN, MARY EILEEN · 2000 to 2014
$39.0M
PAX3/FKHR IN ALVEOLAR RHABDOMYOSARCOMAP01CA071907 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DOWNING, JAMES R · 1996 to 2005
$10.8M
PHARMACOGENOMICS OF CHILDHOOD LEUKEMIA (ALL)R37CA036401 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI EVANS, WILLIAM E · 1987 to 2014
$9.7M
UCLA PHARMACOGENETICS &PHARMACOGENOMICS RESEARCH GROUPU01GM061394 · NIGMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LICINIO, JULIO · 2000 to 2005
$4.7M
PHARMACODYNAMICS OF ANTILEUKEMIC AGENTS IN CHILDRENR01CA078224 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SPARREBOOM, ALEXANDER · 1998 to 2007
$3.6M
P450 METABOLISM OF EPIPODOPHYLLOTOXINS IN CHILDRENR01CA051001 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI RELLING, MARY V. · 1996 to 2006
$2.7M
MicroRNA pharmacogenomics: implications for childhood leukemia (ALL)F32CA141762 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI PAUGH, STEVEN WILLIAM · 2009 to 2011
$157k
NCI NIH HHS 1F32CA141762-01NCI NIH HHS CA21765NCI NIH HHS F32 CA141762NCI NIH HHS P01 CA071907NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA051001NCI NIH HHS R01 CA078224NCI NIH HHS R01 CA51001NCI NIH HHS R01 CA78224NCI NIH HHS R37 CA036401NCI NIH HHS R37 CA36401NIGMS NIH HHS U01 GM061393NIGMS NIH HHS U01 GM061394NIGMS NIH HHS U01 GM61393NIGMS NIH HHS U01 GM61394
6 · The paper itself

Abstract

We investigated whether genetic polymorphisms in the promoter region of the proapoptotic β-2 adrenergic receptor gene (ADRB2) influence treatment-induced changes in ADRB2 expression in leukemia cells and response to chemotherapy. The ADRB2 promoter region was genotyped in germline DNA from 369 children with acute lymphoblastic leukemia (ALL). For 95 of the patients, sufficient RNA was available before and after in vivo treatment to assess treatment-induced gene expression changes in ALL cells. After treatment, the median ADRB2 mRNA expression was ninefold lower in leukemia cells of patients who ultimately relapsed as compared with patients who remained in continuous complete remission (CCR). Polymorphisms in the ADRB2 promoter were significantly linked to methotrexate (MTX)-induced upregulation in ADRB2 gene expression in ALL cells. Moreover, the ADRB2 promoter haplotype was significantly related to early treatment response in 245 children with ALL who received uniform treatment. We conclude that germline polymorphisms in ADRB2 are linked to the antileukemic effects of ALL chemotherapy.

Indexed as

Gene Expression Regulation, NeoplasticAntineoplastic AgentsChildChild, PreschoolFemaleFollow-Up StudiesHumansMalePolymorphism, GeneticPrecursor Cell Lymphoblastic Leukemia-LymphomaPromoter Regions, GeneticReceptors, Adrenergic, beta-2Treatment OutcomeTumor Cells, CulturedADRB2 protein, humanAntineoplastic AgentsReceptors, Adrenergic, beta-2

Identifiers

PMID20981007
PMCPMC3105596
OpenAlexW2020198856

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.