Inoue I

No ORCID on file · 9 papers in corpus · active 2010-2022

Study types

  • article 7
  • review 1

Condition tags

  • endometriosis 8
  • endometrioma 1
article 2022
Journal of human genetics ·doi:10.1038/s10038-021-01003-y

Endometriosis is a benign gynecologic condition, acting as a precursor of certain histological subtypes of ovarian cancers. The epithelial cells of endometriotic tissues and normal uterine endometrium accumulated somatic mutations in cancer…

2022
Nature communications ·doi:10.1038/s41467-022-28568-2

It has become evident that somatic mutations in cancer-associated genes accumulate in the normal endometrium, but spatiotemporal understanding of the evolution and expansion of mutant clones is limited. To elucidate the timing and mechanism…

article 2020
Scientific reports ·doi:10.1038/s41598-020-71273-7

ARID1A loss-of-function mutation accompanied by a loss of ARID1A protein expression is considered one of the most important driver events in endometriosis-associated ovarian cancer. Although our recent genomic study clarified that ARID1A lo…

article 2020
Cancer science ·doi:10.1111/cas.14507

Clear cell carcinoma of the ovary is thought to arise from endometriosis. In addition, retrograde menstruation of shed endometrium is considered the origin of endometriosis. However, little evidence supports cellular continuity from uterine…

article 2019
Human Reproduction ·doi:10.1093/humrep/dez155

STUDY QUESTION: Are there common mutation profiles between epithelial and stromal cells in ovarian endometriotic tissue and the normal endometrium? SUMMARY ANSWER: Our study revealed no common mutations between epithelial and stromal cells …

article 2018
Cell reports ·doi:10.1016/j.celrep.2018.07.037

Endometriosis is characterized by ectopic endometrial-like epithelium and stroma, of which molecular characteristics remain to be fully elucidated. We sequenced 107 ovarian endometriotic and 82 normal uterine endometrial epithelium samples …

article 2016
PLoS genetics ·doi:10.1371/journal.pgen.1005893

Genome-wide association studies (GWASs) have discovered numerous single nucleotide polymorphisms (SNPs) associated with human complex disorders. However, functional characterization of the disease-associated SNPs remains a formidable challe…

article 2013
Journal of human genetics ·doi:10.1038/jhg.2013.32

Our previous genome-wide association study has demonstrated that single-nucleotide polymorphisms (SNPs) located in intronic and downstream regions of IL1A (interleukin 1α) were associated with the risk of endometriosis. These SNPs on the ge…

review 2010
Journal of human genetics ·doi:10.1038/jhg.2010.118

To identify susceptibility genes for endometriosis in Japanese women, genome-wide association (GWA) analysis was performed using two case-control cohorts genotyped with the Affymetrix Mapping 500K Array or Genome-Wide Human SNP Array 6.0. I…