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Title:
Association of H3K9me3 and H3K27me3 repressive histone marks with breast cancer subtypes in the Nursesâ Health Study | Breast Cancer Research and Treatment
Description:
Repressive histone tail modifications have been associated with molecular breast cancer subtypes. We investigated whether histone 3 lysine 9 trimethylation (H3K9me3) and histone 3 lysine 27 trimethylation (H3K27me3) were associated with tumor features and subtypes while adjusting for prospectively collected reproductive and lifestyle breast cancer risk factors. We have tissue microarray data with immunohistochemical marker information on 804 incident cases of invasive breast cancer diagnosed from 1976â2000 in the Nursesâ Health Study. Tissue microarray sections were stained for global H3K9me3 and H3K27me3, and scored into four categories. Multivariate odds ratios (OR) and 95 % confidence intervals (CI) were calculated using logistic regression models for tumor features and subtypes, adjusting for breast cancer risk factors. While there were no significant associations between H3K9me3 and tumor features, H3K27me3 was significantly associated with lower grade tumors compared to high grade tumors in the multivariate model (OR = 1.95, 95 % CI 1.35â2.81, p = 0.0004). H3K27me3 was suggestively associated with estrogen receptor-positive (ER+) tumors (OR = 1.47, 95 % CI 0.97â2.23, p = 0.07). In subtype analyses, H3K27me3 was positively associated with the luminal A subtype compared to all other subtypes (OR = 1.42, 95 % CI 1.14â1.77, p = 0.002), and was inversely associated with HER2-type (OR = 0.58, 95 % CI 0.37â0.91, p = 0.02) and basal-like breast cancer (OR = 0.52, 95 % CI 0.36â0.76, p = 0.0006). In the largest immunohistochemical examination of H3K9me3 and H3K27me3 in breast cancer, we found that H3K27me3 positivity, but not H3K9me3, was associated with lower grade tumors and the luminal A subtype after adjusting for reproductive and lifestyle breast cancer risk factors.
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cancer, breast, pubmed, article, google, scholar, cas, hkme, central, van, histone, study, subtypes, risk, data, health, receptor, res, nature, factors, tamimi, tumor, expression, ezh, usa, analysis, nurses, molecular, trimethylation, grade, access, natl, doinature, privacy, cookies, content, research, association, repressive, epidemiology, hazra, lysine, reproductive, global, estrogen, luminal, triplenegative, clin, liu, oncol,
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month download article/chapter triple-negative breast cancer hr-positive her2-negative stem/progenitor cell signature full article pdf de-identified data sets progesterone receptor status estrogen receptor-positive breast cancer risk breast cancer risk familial breast cancer pathology tissue-chromatin immunoprecipitation privacy choices/manage cookies state cancer registries garcia-closas independent prognostic factor breast epithelial cells hormonal risk factors millikan rc human breast tumours single nucleotide polymorphisms breast cancer defined aggressive breast cancer inflammatory breast cancer androgen receptor expression breast cancer prognosis lakhani sr gene expression patterns cancer prev res reproductive risk factors van de vijver breast cancer subtypes polycomb complex prc2 human investigations committee protect human subjects nursesâ health study harvard medical school institutional review boards breast cancer associations alter gene expression largest immunohistochemical examination dna hypermethylation module tumour dna ploidy tissue microarray sections renal cell carcinoma van de rijn van leeuwen fe van den ouweland high ezh2 expression bmc cancer 13
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headline:Association of H3K9me3 and H3K27me3 repressive histone marks with breast cancer subtypes in the Nursesâ Health Study
description:Repressive histone tail modifications have been associated with molecular breast cancer subtypes. We investigated whether histone 3 lysine 9 trimethylation (H3K9me3) and histone 3 lysine 27 trimethylation (H3K27me3) were associated with tumor features and subtypes while adjusting for prospectively collected reproductive and lifestyle breast cancer risk factors. We have tissue microarray data with immunohistochemical marker information on 804 incident cases of invasive breast cancer diagnosed from 1976â2000 in the Nursesâ Health Study. Tissue microarray sections were stained for global H3K9me3 and H3K27me3, and scored into four categories. Multivariate odds ratios (OR) and 95 % confidence intervals (CI) were calculated using logistic regression models for tumor features and subtypes, adjusting for breast cancer risk factors. While there were no significant associations between H3K9me3 and tumor features, H3K27me3 was significantly associated with lower grade tumors compared to high grade tumors in the multivariate model (OR = 1.95, 95 % CI 1.35â2.81, p = 0.0004). H3K27me3 was suggestively associated with estrogen receptor-positive (ER+) tumors (OR = 1.47, 95 % CI 0.97â2.23, p = 0.07). In subtype analyses, H3K27me3 was positively associated with the luminal A subtype compared to all other subtypes (OR = 1.42, 95 % CI 1.14â1.77, p = 0.002), and was inversely associated with HER2-type (OR = 0.58, 95 % CI 0.37â0.91, p = 0.02) and basal-like breast cancer (OR = 0.52, 95 % CI 0.36â0.76, p = 0.0006). In the largest immunohistochemical examination of H3K9me3 and H3K27me3 in breast cancer, we found that H3K27me3 positivity, but not H3K9me3, was associated with lower grade tumors and the luminal A subtype after adjusting for reproductive and lifestyle breast cancer risk factors.
datePublished:2014-09-16T00:00:00Z
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H3K9me3
H3K27me3
Histone methylation
Breast cancer
Subtype
Risk factor
Oncology
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headline:Association of H3K9me3 and H3K27me3 repressive histone marks with breast cancer subtypes in the Nursesâ Health Study
description:Repressive histone tail modifications have been associated with molecular breast cancer subtypes. We investigated whether histone 3 lysine 9 trimethylation (H3K9me3) and histone 3 lysine 27 trimethylation (H3K27me3) were associated with tumor features and subtypes while adjusting for prospectively collected reproductive and lifestyle breast cancer risk factors. We have tissue microarray data with immunohistochemical marker information on 804 incident cases of invasive breast cancer diagnosed from 1976â2000 in the Nursesâ Health Study. Tissue microarray sections were stained for global H3K9me3 and H3K27me3, and scored into four categories. Multivariate odds ratios (OR) and 95 % confidence intervals (CI) were calculated using logistic regression models for tumor features and subtypes, adjusting for breast cancer risk factors. While there were no significant associations between H3K9me3 and tumor features, H3K27me3 was significantly associated with lower grade tumors compared to high grade tumors in the multivariate model (OR = 1.95, 95 % CI 1.35â2.81, p = 0.0004). H3K27me3 was suggestively associated with estrogen receptor-positive (ER+) tumors (OR = 1.47, 95 % CI 0.97â2.23, p = 0.07). In subtype analyses, H3K27me3 was positively associated with the luminal A subtype compared to all other subtypes (OR = 1.42, 95 % CI 1.14â1.77, p = 0.002), and was inversely associated with HER2-type (OR = 0.58, 95 % CI 0.37â0.91, p = 0.02) and basal-like breast cancer (OR = 0.52, 95 % CI 0.36â0.76, p = 0.0006). In the largest immunohistochemical examination of H3K9me3 and H3K27me3 in breast cancer, we found that H3K27me3 positivity, but not H3K9me3, was associated with lower grade tumors and the luminal A subtype after adjusting for reproductive and lifestyle breast cancer risk factors.
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H3K9me3
H3K27me3
Histone methylation
Breast cancer
Subtype
Risk factor
Oncology
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- https://doi.org/10.1371%2Fjournal.pgen.1000054's financial summary
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