Cargando…

Familial risk of epithelial ovarian cancer after accounting for gynaecological surgery: a population-based study

BACKGROUND: Uptake of risk-reducing surgery has increased among women at high risk of epithelial ovarian cancer. We sought to characterise familial risk of epithelial ovarian cancer histotypes in a population-based study after accounting for gynaecological surgeries, including bilateral oophorectomy...

Descripción completa

Detalles Bibliográficos
Autores principales:	Barnard, Mollie E, Meeks, Huong, Jarboe, Elke A, Albro, James, Camp, Nicola J, Doherty, Jennifer A
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BMJ Publishing Group 2023
Materias:	Cancer Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643667/ https://www.ncbi.nlm.nih.gov/pubmed/35534206 http://dx.doi.org/10.1136/jmedgenet-2021-108402

Ejemplares similares

Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap
por: McCuaig, Jeanna M, et al.
Publicado: (2018)

New paradigms for BRCA1/BRCA2 testing in women with ovarian cancer: results of the Genetic Testing in Epithelial Ovarian Cancer (GTEOC) study
por: Plaskocinska, Inga, et al.
Publicado: (2016)

Comprehensive epithelial tubo-ovarian cancer risk prediction model incorporating genetic and epidemiological risk factors
por: Lee, Andrew, et al.
Publicado: (2022)

A risk prediction algorithm for ovarian cancer incorporating BRCA1, BRCA2, common alleles and other familial effects
por: Jervis, Sarah, et al.
Publicado: (2015)

MSH2 is the very young onset ovarian cancer predisposition gene, not BRCA1
por: Flaum, Nicola, et al.
Publicado: (2023)

Assessment of mismatch repair deficiency in ovarian cancer
por: Crosbie, Emma J, et al.
Publicado: (2021)

Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer
por: Song, Honglin, et al.
Publicado: (2021)

17β-estradiol upregulates GREB1 and accelerates ovarian tumor progression in vivo
por: Laviolette, Laura A, et al.
Publicado: (2014)

Evaluation of polygenic risk scores for ovarian cancer risk prediction in a prospective cohort study
por: Yang, Xin, et al.
Publicado: (2018)

Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma
por: Potjer, Thomas P, et al.
Publicado: (2021)

Colorectal cancer intrinsic subtypes predict chemotherapy benefit, deficient mismatch repair and epithelial-to-mesenchymal transition
por: Roepman, Paul, et al.
Publicado: (2014)

Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants
por: Puntervoll, Hanne Eknes, et al.
Publicado: (2013)

Intake of dietary flavonoids and risk of epithelial ovarian cancer(1)(2)(3)(4)
por: Cassidy, Aedín, et al.
Publicado: (2014)

High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families
por: Helgadottir, Hildur, et al.
Publicado: (2014)

The avoiding late diagnosis of ovarian cancer (ALDO) project; a pilot national surveillance programme for women with pathogenic germline variants in BRCA1 and BRCA2
por: Philpott, Sue, et al.
Publicado: (2023)

Methylation status of oestrogen receptor-α gene promoter sequences in human ovarian epithelial cell lines
por: O'Doherty, A M, et al.
Publicado: (2002)

Transcript capture and ultradeep long-read RNA sequencing (CAPLRseq) to diagnose HNPCC/Lynch syndrome
por: Schwenk, Vincent, et al.
Publicado: (2023)

Significance of lymphovascular space invasion in epithelial ovarian cancer
por: Matsuo, Koji, et al.
Publicado: (2012)

Recurrent moderate‐risk mutations in Finnish breast and ovarian cancer patients
por: Nurmi, Anna, et al.
Publicado: (2019)

LncRNA SRA mediates cell migration, invasion, and progression of ovarian cancer via NOTCH signaling and epithelial–mesenchymal transition
por: Kim, Lee Kyung, et al.
Publicado: (2021)

Improving Short- and Long-Term Genetic Gain by Accounting for Within-Family Variance in Optimal Cross-Selection
por: Allier, Antoine, et al.
Publicado: (2019)

Endometrial Cancers Harboring Mutated Fibroblast Growth Factor Receptor 2 Protein Are Successfully Treated With a New Small Tyrosine Kinase Inhibitor in an Orthotopic Mouse Model
por: Taurin, Sebastien, et al.
Publicado: (2018)

An estrogen-induced endometrial hyperplasia mouse model recapitulating human disease progression and genetic aberrations
por: Yang, Chieh-Hsiang, et al.
Publicado: (2015)

Identification of novel cyclin gene fusion transcripts in endometrioid ovarian carcinomas
por: Agostini, Antonio, et al.
Publicado: (2018)

High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer
por: Evans, D Gareth, et al.
Publicado: (2022)

Distinct methylation profile of mucinous ovarian carcinoma reveals susceptibility to proteasome inhibitors
por: Liew, Phui‐Ly, et al.
Publicado: (2018)

GOLPH3 induces epithelial–mesenchymal transition via Wnt/β‐catenin signaling pathway in epithelial ovarian cancer
por: Sun, Jing, et al.
Publicado: (2017)

Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility
por: Weren, Robbert D A, et al.
Publicado: (2018)

Expression of Tissue Factor in Epithelial Ovarian Carcinoma Is Involved in the Development of Venous Thromboembolism
por: Sakurai, Manabu, et al.
Publicado: (2017)

LGR5 promotes epithelial ovarian cancer proliferation, metastasis, and epithelial–mesenchymal transition through the Notch1 signaling pathway
por: Liu, Wenxue, et al.
Publicado: (2018)

Characterization of the Potential Role of NTPCR in Epithelial Ovarian Cancer by Integrating Transcriptomic and Metabolomic Analysis
por: Shang, Hongkai, et al.
Publicado: (2021)

Germline mutations in WNK2 could be associated with serrated polyposis syndrome
por: Soares de Lima, Yasmin, et al.
Publicado: (2023)

Integrated Analysis of Prognostic and Immune Associated Integrin Family in Ovarian Cancer
por: Wu, Anqi, et al.
Publicado: (2020)

Multiple synchronous sites of origin of vestibular schwannomas in neurofibromatosis Type 2
por: Stivaros, Stavros M, et al.
Publicado: (2015)

Epithelial ovarian cancer subtypes attributable to smoking in the Norwegian Women and Cancer Study, 2012
por: Licaj, Idlir, et al.
Publicado: (2016)

Identification of Potential Biomarkers in Association With Progression and Prognosis in Epithelial Ovarian Cancer by Integrated Bioinformatics Analysis
por: Liu, Jinhui, et al.
Publicado: (2019)

The actin bundling activity of ITPKA mainly accounts for its migration-promoting effect in lung cancer cells
por: Küster, Lukas, et al.
Publicado: (2023)

Integrated molecular profiling of patient‐derived ovarian cancer models identifies clinically relevant signatures and tumor vulnerabilities
por: Lupia, Michela, et al.
Publicado: (2022)

Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD
por: Andrews, Katrina A, et al.
Publicado: (2018)

Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions
por: Barrett, Jennifer H, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_2deodg6s4oged42c3qmguk1gkt