Kang S

ORCID: 0000-0003-1542-9750 · 38 papers in corpus
observational 2026
Scientific reports ·doi:10.1038/s41598-025-33836-4

Per- and polyfluoroalkyl substances (PFAS) have been previously associated with polycystic ovary syndrome (PCOS). However, the health effects of emerging PFAS alternatives on PCOS remain unclear. This study aims to examine the associations …

other 2026
Clinical epigenetics ·doi:10.1186/s13148-026-02161-6

BACKGROUND: Uterine adenomatoid tumors (UATs) are rare benign mesothelial neoplasms with poorly characterized molecular features. Comprehensive genomic profiling of UATs remains limited. METHODS: Targeted sequencing of 20 pathologically co…

review 2026
Archives of gynecology and obstetrics ·doi:10.1007/s00404-025-08257-3

BACKGROUND: Salpingitis is a leading cause of female infertility and ectopic pregnancy worldwide. Despite advances in reproductive medicine, its early diagnosis and effective prevention of long-term sequelae remain challenging due to its of…

review 2026
Microbial biotechnology ·doi:10.1111/1751-7915.70330

Infertility affects ~1 in 6 people of reproductive age and remains difficult to treat because causes are heterogeneous and diagnostics are incomplete. Recent evidence reframes the female reproductive tract as a low-biomass but biologically …

other 2026
International journal of general medicine ·doi:10.2147/ijgm.s586914

BACKGROUND: Immature teratoma is a malignant tumor and accounts for 1%-3% of ovary teratoma. The objective of this study was to find the potential single nucleotide polymorphisms (SNPs), copy number variations (CNVs) and drug targets in the…

lab-animal 2025
Gene ·doi:10.1016/j.gene.2025.149385

BACKGROUND: Emerging evidence suggests that aberrantly expressed microRNAs (miRNAs) participate in endometriosis pathogenesis. miR-1229-5p participates in the pathogenesis of several disease, but its precise role and mechanism in endometrio…

review 2024
Cells ·doi:10.3390/cells13161354

Autophagy, an evolutionarily conserved cellular mechanism essential for maintaining internal stability, plays a crucial function in female reproductive ability. In this review, we discuss the complex interplay between autophagy and several …

other 2024
Medicine ·doi:10.1097/MD.0000000000040690

Endometriosis (EMs) is a common gynecological disease accompanied by metabolic disturbances. However, the causality between metabolites and the risk of EMs remains unclear. We conducted a 2-sample Mendelian randomization (MR) analysis using…

observational 2024
Scientific reports ·doi:10.1038/s41598-024-52822-w

This study aimed to detect signals of adverse drug reactions (ADRs) associated with biological disease-modifying antirheumatic drugs (DMARDs) and targeted therapies in rheumatoid arthritis (RA) and ankylosing spondylitis (AS) patients. Util…

observational 2024
iScience ·doi:10.1016/j.isci.2024.110896

Based on analyses of 22,487,947 person-years of follow-up data in a cohort of 2,523,565 young females, we found that the presence of depression was associated with a higher cumulative incidence of new-onset uterine leiomyoma than the absenc…

other 2024
Frontiers in immunology ·doi:10.3389/fimmu.2024.1507083

BACKGROUND: Ferroptosis, a recently discovered iron-dependent cell death, is linked to various diseases but its role in endometriosis is still not fully understood. METHODS: In this study, we integrated microarray data of endometriosis fro…

observational 2024
Frontiers in oncology ·doi:10.3389/fonc.2024.1510988

INTRODUCTION: Women with low-risk endometrial cancer, as defined by the Korean Gynecologic Oncology Group (KGOG) criteria, have a low risk of lymph node metastasis and an excellent prognosis without lymphadenectomy. However, it is unclear w…

case-report 2023
BMC women's health ·doi:10.1186/s12905-023-02741-1

BACKGROUND: In the past, the primary treatment for MRKH syndrome (Mayer-Rokitansky-Küster-Hauser syndrome) with a functional primordial uterus was surgical removal of the functional primordial uterus. In rare instances, the endometrium of t…

other 2023
Biomolecules & biomedicine ·doi:10.17305/bb.2023.9989

Growing evidence indicates that aberrant methylation is pivotal in the development and progression of endometriosis (EMs). This study explores the relationship between abnormal methylation of the ENPP3 promoter and the pathogenesis of ovari…

observational 2022
BMC cancer ·doi:10.1186/s12885-022-10288-x

BACKGROUND: Ureteral reconstruction is required after surgical resection of the tumor invading the urinary tract in ovarian cancer with low incidence. There are no currently reported surgical outcomes of ureteral reconstruction during cytor…

observational 2021
Public health genomics ·doi:10.1159/000517266

BACKGROUND: The aim of the study was to investigate the role of the genetic variation of glutathione S-transferase M1 (GSTM1) in the development of ovarian endometriosis and endometriosis-related primary infertility risk. METHODS: This cas…

observational 2020
·doi:10.22541/au.160253851.14434237/v1

Objective To investigate the surgical effort of endometriosis the in the surgical management of early ovarian cancer. Design: A retrospective study Setting National Cancer Center Population All women who underwent cytoreductive surgery betw…

observational 2020
Journal of ovarian research ·doi:10.1186/s13048-020-00698-5

PURPOSE: We investigated the effect of ovary preserving surgery in early International Federation of Obstetrics and Gynecology (FIGO) stage endometrial cancer patients. METHODS: Medical records were retrospectively reviewed for 539 patient…

observational 2019
Human Reproduction ·doi:10.1093/humrep/dez039

STUDY QUESTION: Is the methylation status of the glutathione S-transferase M1 (GSTM1) promoter region altered in patients with ovarian endometriosis, and does this affect the expression of GSTM1 in their endometrial tissues? SUMMARY ANSWER…

observational 2018
Gene ·doi:10.1016/j.gene.2018.04.082

OBJECTIVE: To explore the role of functional genetic variant of IL12B in the pathogenesis of ovarian endometriosis. STUDY DESIGN: This study included 815 patients with ovarian endometriosis and 788 women in the control group. Two polymorph…

observational 2017
Reproductive sciences (Thousand Oaks, Calif.) ·doi:10.1177/1933719116650753

Endometriosis is a common multifactorial disease caused by an interaction between multiple gene loci and environment. Four genome-wide association studies (GWASs) of endometriosis have identified several single-nucleotide polymorphisms (SNP…

observational 2017
Yonsei medical journal ·doi:10.3349/ymj.2017.58.1.59

PURPOSE: Loss of AT-rich DNA-interacting domain 1A (ARID1A) has been identified as a driving mutation of ovarian clear cell carcinoma (O-CCC), a triple-negative ovarian cancer that is intermediary between serous and endometrioid subtypes, i…

2016
Journal of therapeutic ultrasound
other 2016
Gynecologic and obstetric investigation ·doi:10.1159/000445293

The loss of E-cadherin expression plays an important role in the development of endometriosis, but the molecular mechanism is not clear to date. It has been confirmed that the hypermethylation of the CpG island may be an important molecular…

observational 2015
Biomedical reports ·doi:10.3892/br.2015.511

The first tumor metastasis-suppressor gene, nm23, may have an important role in the pathogenesis of endometriosis (EM). The present study aimed to evaluate whether nm23 gene polymorphisms are correlated with the risk of the development of E…