Evidence map›Paper›PMID 23526707›Full record

ArticlePharmacogenomics and personalized medicine2013

Copy number variation in sulfotransferase isoform 1A1 (SULT1A1) is significantly associated with enzymatic activity in Japanese subjects.

Xinfeng Yu, Takahiro Kubota, Ishwori Dhakal, Setsuo Hasegawa, Suzanne Williams, Shogo Ozawa, Susan Kadlubar

Open access · goldAbstract read
In one paragraph

Article in Pharmacogenomics and personalized medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Influence ofPharmacogenomics and personalized medicine · 2021
    Article
  5. Article
  6. Review
  7. Relationship of SULT1A1 copy number variation with estrogen metabolism and human health.The Journal of steroid biochemistry and molecular biology · 2017
    Article
  8. Review
  9. Article
  10. Article
  11. Pharmacogenetics of SULT1A1.Pharmacogenomics · 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

7 authors at 3 institutions in 2 countries.

Xinfeng YuDivision of Medical Genetics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA;
Takahiro Kubota
Ishwori Dhakal
Setsuo Hasegawa
Suzanne Williams
Shogo Ozawa
Susan Kadlubar
University of Arkansas for Medical Sciences · USChiba Institute of Science · JPIwate Medical University · JP

Funding

Regulation of SULT1A1 in Human BreastR01CA128897 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI KADLUBAR, SUSAN A. · 2008 to 2012
$2.0M
NCI NIH HHS R01 CA128897
6 · The paper itself

Abstract

Sulfotransferase isoform 1A1 (SULT1A1) plays a key role in the metabolism of a variety of endo- and xenobiotics and it's activity could influence response to drugs. Our previous studies have focused on the impact of genetic variants of SULT1A1 on enzymatic activity in Caucasians and African-Americans. However, the contribution of genetic variants to SULT1A1 activity in Asians has not been explored. In this study, we investigated the collective effects of both SULT1A1 copy number variants (CNVs) and single nucleotide polymorphisms (SNPs) in the promoter region, coding region, and 3' untranslated region on SULT1A1 activity in Japanese subjects. SNPs in the SULT1A1 promoter and 3' untranslated region were not associated with SULT1A1 activity (P > 0.05). SULT1A1*1/2 (Arg213His) was marginally associated with SULT1A1 activity (P = 0.037). However, SULT1A1 CNVs were strongly associated with SULT1A1 activity (trend test P = 0.008) and accounted for 10% of the observed variability in activity for Japanese subjects. In conclusion, SULT1A1 CNVs play a pivotal role in determination of SULT1A1 activity in Japanese subjects, highlighting the influence of ethnic differences in SULT1A1 genetic variants on drug metabolism and therapeutic efficacy.

Indexed as

CNVgenotypephenotypesingle nucleotide polymorphismsSULT1A1

Identifiers

PMID23526707
PMCPMC3596141
OpenAlexW1689874202

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.