Abstract 2125: Roles of KAT6A and KAT6B in the biology of estrogen positive breast cancer

癌症研究 癌症 生物 基因表达 乳腺癌 雌激素受体 细胞生长 癌细胞 细胞培养 基因 遗传学
作者
Isabelle Meaux,Dimitri Gorge-Bernat,A Garcia De La Paz,Catherine Geslin,Laurent Debussche,Jürgen Moll,Christophe Henry
出处
期刊:Cancer Research [American Association for Cancer Research]
卷期号:81 (13_Supplement): 2125-2125
标识
DOI:10.1158/1538-7445.am2021-2125
摘要

Abstract KAT6A and KAT6B are histone acetyl transferase (HAT) that are controlling gene expression by transferring acetyl groups to histones. Yu et al (Oncogene, 2017 36, 2910-2918) have shown that KAT6A has a role in breast cancer development by activating the ERα promoter and was found frequently amplified in 11% and is overexpressed in 15% of breast cancers. Altogether, these data support KAT6A as an attractive target in estrogen receptor driven breast cancer. KAT6B is a close homolog that shares 91% identity in the acetyl coA binding site. While the prevalence of gene amplification for KAT6B in breast cancer is only 1-2%, it is often overexpressed. In this study, we are exploring how KAT6A and KAT6B are contributing to ERα expression and the growth of KAT6A amplified breast cancer cell lines. To decipher each protein's role, we have designed specific siRNA against KAT6A and KAT6B and we tested their action either individually or in combination in the KAT6A gene amplified breast cancer cell lines T-47D, CAM-1 and ZR-75. Following treatment of T-47D, CAMA-1 and ZR75 cell lines with KAT6A or B siRNA we observed a decrease of ERα gene and protein expression for all siRNAs. The effect was more pronounced when using KAT6A over KAT6B and the effect of both siRNA A/B were additive. Phenotypically, the impact on cell line proliferation by applying clonogenic and incucyte assays, mirrors what is observed on ERα gene and protein expression. The effect on cellular proliferation of KAT6A is more prominent than KAT6B silencing, while the combined KAT6A + KAT6B silencing being more impactful than KAT6A silencing alone. In conclusion, our data show that KAT6A and KAT6B share similar function in the control of ER gene and protein expression. This study suggests that KAT6A and KAT6B may be paralogs, one compensating for the loss of the other. This translates into a more pronounced antiproliferative effect when both genes are silenced concomitantly. Citation Format: Isabelle Meaux, Dimitri Gorge-Bernat, Angele Paz, Catherine Geslin, Laurent Debussche, Jürgen Moll, Christophe Henry. Roles of KAT6A and KAT6B in the biology of estrogen positive breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2125.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
menghuigucha完成签到,获得积分10
3秒前
5秒前
桐桐应助sian采纳,获得10
5秒前
星辰大海应助tmuguoli采纳,获得10
6秒前
醉熏的天薇完成签到,获得积分10
6秒前
啊啊啊完成签到,获得积分10
6秒前
111发布了新的文献求助10
6秒前
华仔应助menghuigucha采纳,获得10
7秒前
想看不眠日记完成签到,获得积分10
8秒前
WXR0721完成签到 ,获得积分10
8秒前
寒食应助西瘡采纳,获得30
8秒前
天天快乐应助大力日记本采纳,获得10
8秒前
桂花酒酿完成签到,获得积分10
9秒前
斯文败类应助keyantong采纳,获得10
12秒前
13秒前
13秒前
14秒前
Lucas应助cccyyy采纳,获得10
15秒前
16秒前
简单绯应助聪明的宛菡采纳,获得10
17秒前
wanci应助111采纳,获得10
17秒前
songzi完成签到,获得积分20
18秒前
18秒前
mawanyu发布了新的文献求助10
20秒前
20秒前
优雅梦曼发布了新的文献求助50
20秒前
linan发布了新的文献求助10
21秒前
22秒前
小白发布了新的文献求助50
22秒前
xw完成签到,获得积分10
25秒前
27秒前
27秒前
27秒前
27秒前
LZCCC完成签到,获得积分10
28秒前
Leo完成签到,获得积分10
28秒前
活力的曼柔完成签到,获得积分20
29秒前
w_完成签到,获得积分10
30秒前
汉堡包应助coral采纳,获得10
30秒前
30秒前
高分求助中
Rock-Forming Minerals, Volume 3C, Sheet Silicates: Clay Minerals 2000
The late Devonian Standard Conodont Zonation 2000
Nickel superalloy market size, share, growth, trends, and forecast 2023-2030 2000
The Lali Section: An Excellent Reference Section for Upper - Devonian in South China 1500
Very-high-order BVD Schemes Using β-variable THINC Method 930
The Healthy Socialist Life in Maoist China 600
Development of general formulas for bolted flanges, by E.O. Waters [and others] 600
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3266638
求助须知:如何正确求助?哪些是违规求助? 2906358
关于积分的说明 8337686
捐赠科研通 2576748
什么是DOI,文献DOI怎么找? 1400715
科研通“疑难数据库(出版商)”最低求助积分说明 654888
邀请新用户注册赠送积分活动 633770