Integrative Single-Cell Analysis Reveals Transcriptional and Epigenetic Regulatory Features of Clear Cell Renal Cell Carcinoma

肾透明细胞癌 染色质 生物 表观遗传学 转录组 计算生物学 细胞 表观遗传学 基因 癌症研究 基因表达 遗传学 DNA甲基化 肾细胞癌 医学 病理
作者
Zhenyuan Yu,Yufang Lv,Cheng Su,Wenhao Lu,RuiRui Zhang,Jiaping Li,Bingqian Guo,Haibiao Yan,Deyun Liu,Zhanbin Yang,Hua Mi,Linjian Mo,Yi Guo,Wenyu Feng,Haotian Xu,Wenyi Peng,Jiwen Cheng,Aruo Nan,Zengnan Mo
出处
期刊:Cancer Research [American Association for Cancer Research]
卷期号:83 (5): 700-719 被引量:35
标识
DOI:10.1158/0008-5472.can-22-2224
摘要

Abstract Clear cell renal cell carcinoma (ccRCC) frequently features a high level of tumor heterogeneity. Elucidating the chromatin landscape of ccRCC at the single-cell level could provide a deeper understanding of the functional states and regulatory dynamics underlying the disease. Here, we performed single-cell RNA sequencing (scRNA-seq) and single-cell assay for transposase-accessible chromatin using sequencing (scATAC-seq) on 19 ccRCC samples, and whole-exome sequencing was used to understand the heterogeneity between individuals. Single-cell transcriptome and chromatin accessibility maps of ccRCC were constructed to reveal the regulatory characteristics of different tumor cell subtypes in ccRCC. Two long noncoding RNAs (RP11-661C8.2 and CTB-164N12.1) were identified that promoted the invasion and migration of ccRCC, which was validated with in vitro experiments. Taken together, this study comprehensively characterized the gene expression and DNA regulation landscape of ccRCC, which could provide new insights into the biology and treatment of ccRCC. Significance: A comprehensive analysis of gene expression and DNA regulation in ccRCC using scATAC-seq and scRNA-seq reveals the DNA regulatory programs of ccRCC at the single-cell level.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
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
墨墨Daisy完成签到,获得积分20
刚刚
刚刚
LUCKYLI_QIAN发布了新的文献求助10
刚刚
格纹完成签到,获得积分10
刚刚
1秒前
眼睛这么小完成签到,获得积分10
1秒前
不安香水关注了科研通微信公众号
1秒前
2秒前
3秒前
3秒前
3秒前
3秒前
直率乐瑶完成签到,获得积分20
4秒前
4秒前
勤劳惜天关注了科研通微信公众号
5秒前
5秒前
6秒前
6秒前
6秒前
6秒前
NexusExplorer应助yam采纳,获得10
7秒前
梦雪完成签到,获得积分10
8秒前
斯文败类应助筱娟采纳,获得10
8秒前
Auunes发布了新的文献求助10
9秒前
9秒前
感动书竹发布了新的文献求助10
9秒前
hivivian发布了新的文献求助10
10秒前
哈哈发布了新的文献求助10
10秒前
所所应助Amanda采纳,获得10
10秒前
踏实的惋庭完成签到,获得积分10
11秒前
11秒前
量子星尘发布了新的文献求助10
11秒前
11秒前
科研通AI2S应助紧张的问薇采纳,获得10
11秒前
YY完成签到,获得积分10
11秒前
12秒前
JamesPei应助搞怪的水彤采纳,获得30
12秒前
Y神发布了新的文献求助10
12秒前
JamesPei应助知知采纳,获得10
12秒前
梦雪发布了新的文献求助10
13秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 3000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
Social Work and Social Welfare: An Invitation(7th Edition) 410
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6055565
求助须知:如何正确求助?哪些是违规求助? 7883470
关于积分的说明 16287637
捐赠科研通 5200813
什么是DOI,文献DOI怎么找? 2782822
邀请新用户注册赠送积分活动 1765688
关于科研通互助平台的介绍 1646630