Evidence map›Paper›PMID 22180457›Full record

ArticleHuman molecular genetics2012

A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese.

Kazuma Kiyotani, Taisei Mushiroda, Tatsuhiko Tsunoda, Takashi Morizono, Naoya Hosono, Michiaki Kubo, Yusuke Tanigawara, Chiyo K Imamura, David A Flockhart, Fuminori Aki and 8 more

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Article in Human molecular genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 7 pooled it
–field-weighted citation impact
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

28 citing papers in PubMed, 7 syntheses or guidelines pooled it.

  1. Pooled it
  2. Polymorphism at 19q13.41 Predicts Breast Cancer Survival Specifically after Endocrine Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Kazuma KiyotaniLaboratory for Pharmacogenetics, RIKEN Center for Genomic Medicine, Yokohama 230-0045, Japan.
Taisei Mushiroda
Tatsuhiko Tsunoda
Takashi Morizono
Naoya Hosono
Michiaki Kubo
Yusuke Tanigawara
Chiyo K Imamura
David A Flockhart
Fuminori Aki
Koichi Hirata
Yuichi Takatsuka
Minoru Okazaki
Shozo Ohsumi
Takashi Yamakawa
Mitsunori Sasa
Yusuke Nakamura
Hitoshi Zembutsu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although many association studies of polymorphisms in candidate genes with the clinical outcomes of breast cancer patients receiving adjuvant tamoxifen therapy have been reported, genetic factors determining individual response to tamoxifen are not fully understood. To identify genetic polymorphisms associated with clinical outcomes of patients with tamoxifen treatment, we conducted a genome-wide association study (GWAS). We studied 462 Japanese patients with hormone receptor-positive, invasive breast cancer receiving adjuvant tamoxifen therapy. Of them, 240 patients were analyzed by genome-wide genotyping using the Illumina Human610-Quad BeadChips, and two independent sets of 105 and 117 cases were used for replication studies. In the GWAS, we detected significant associations with recurrence-free survival at 15 single-nucleotide polymorphisms (SNPs) on nine chromosomal loci (1p31, 1q41, 5q33, 7p11, 10q22, 12q13, 13q22, 18q12 and 19p13) that satisfied a genome-wide significant threshold (log-rank P= 2.87 × 10(-9)-9.41 × 10(-8)). Among them, rs10509373 in C10orf11 gene on 10q22 was significantly associated with recurrence-free survival in the replication study (log-rank P= 2.02 × 10(-4)) and a combined analysis indicated a strong association of this SNP with recurrence-free survival in breast cancer patients treated with tamoxifen (log-rank P= 1.26 × 10(-10)). Hazard ratio per C allele of rs10509373 was 4.51 [95% confidence interval (CI), 2.72-7.51; P= 6.29 × 10(-9)]. In a combined analysis of rs10509373 genotype with previously identified genetic makers, CYP2D6 and ABCC2, the number of risk alleles of these three genes had cumulative effects on recurrence-free survival among 345 patients receiving tamoxifen monotherapy (log-rank P= 2.28 × 10(-12)). In conclusion, we identified a novel locus associated with recurrence-free survival in Japanese breast cancer patients receiving adjuvant tamoxifen therapy.

Indexed as

Chromosomes, Human, Pair 10Genetic LociPolymorphism, Single NucleotideAdultAgedAged, 80 and overAntineoplastic Agents, HormonalBreast NeoplasmsDisease-Free SurvivalFemaleGenome-Wide Association StudyHumansJapanMiddle AgedMultidrug Resistance-Associated Protein 2TamoxifenABCC2 protein, humanAntineoplastic Agents, HormonalMultidrug Resistance-Associated Protein 2Tamoxifen

Identifiers

PMID22180457

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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.