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量化 Tip60(Kat5)可分层乳腺癌。

Quantifying Tip60 (Kat5) stratifies breast cancer.

机构信息

Discipline of Surgery, School of Medicine, Lambe institute for Translational Research, National University of Ireland, Galway, Ireland.

School of Mathematics, Statistics and Applied Mathematics, National University of Ireland, Galway, Ireland.

出版信息

Sci Rep. 2019 Mar 7;9(1):3819. doi: 10.1038/s41598-019-40221-5.

Abstract

Breast cancer is stratified into four distinct clinical subtypes, using three key biomarkers (Her2/Neu gene status, Estrogen and Progesterone receptor status). However, each subtype is a heterogeneous group, displaying significant variation in survival rates and treatment response. New biomarkers are required to provide more precise stratification of breast cancer cohorts to inform personalised treatment options/predict outcomes. Tip60 is a member of the MYST sub-family of histone acetyltransferases (HATs), and is directly involved in genome maintenance, gene regulation and DNA damage response/repair pathways (key chemotherapeutic influencing mechanisms). We aimed to determine if quantifying Tip60 staining patterns improved breast cancer stratification. We defined Tip60 protein in vivo, quantifying location (cytoplasmic, nuclear), percent of cells and staining intensity in a breast cancer tissue microarray (n = 337). A significant association of specific Tip60 staining patterns with breast cancer subtype, ER or PR status and Tumour grade was found. Importantly, low Tip60 mRNA expression correlated with poor overall survival and relapse free survival. We found Tip60 is a biomarker able to stratify breast cancer patients, and low Tip60 expression is a significant risk factor indicating a higher chance of disease reoccurrence. This work highlights Tip60 regulation as a key factor influencing the development of breast cancer.

摘要

乳腺癌分为四个不同的临床亚型,使用三个关键的生物标志物(Her2/neu 基因状态、雌激素和孕激素受体状态)。然而,每个亚型都是一个异质群体,在生存率和治疗反应方面存在显著差异。需要新的生物标志物来更精确地对乳腺癌队列进行分层,以提供个性化的治疗选择/预测结果。Tip60 是组蛋白乙酰转移酶(HATs)的 MYST 亚家族的成员,直接参与基因组维护、基因调控和 DNA 损伤反应/修复途径(关键的化疗影响机制)。我们旨在确定定量 Tip60 染色模式是否能改善乳腺癌的分层。我们在乳腺癌组织微阵列中(n=337)定义了 Tip60 蛋白的体内位置(细胞质、核)、细胞百分比和染色强度。发现特定的 Tip60 染色模式与乳腺癌亚型、ER 或 PR 状态和肿瘤分级之间存在显著关联。重要的是,低 Tip60mRNA 表达与总生存和无病生存不良相关。我们发现 Tip60 是一种能够对乳腺癌患者进行分层的生物标志物,低表达 Tip60 是疾病复发的一个重要危险因素,表明复发的可能性更高。这项工作强调了 Tip60 调节作为影响乳腺癌发展的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa47/6405843/3da48cb2e8ad/41598_2019_40221_Fig1_HTML.jpg

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