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BRD3 作为表观遗传调控因子在结直肠癌中发挥抑瘤作用。

Tumor suppressive role of the epigenetic master regulator BRD3 in colorectal cancer.

机构信息

Department of Surgery, Kyushu University Beppu Hospital, Beppu, Japan.

Department of Gastroenterological Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

出版信息

Cancer Sci. 2024 Jun;115(6):1866-1880. doi: 10.1111/cas.16129. Epub 2024 Mar 17.

Abstract

Bromodomain and extraterminal domain (BET) family proteins are epigenetic master regulators of gene expression via recognition of acetylated histones and recruitment of transcription factors and co-activators to chromatin. Hence, BET family proteins have emerged as promising therapeutic targets in cancer. In this study, we examined the functional role of bromodomain containing 3 (BRD3), a BET family protein, in colorectal cancer (CRC). In vitro and vivo analyses using BRD3-knockdown or BRD3-overexpressing CRC cells showed that BRD3 suppressed tumor growth and cell cycle G1/S transition and induced p21 expression. Clinical analysis of CRC datasets from our hospital or The Cancer Genome Atlas revealed that BET family genes, including BRD3, were overexpressed in tumor tissues. In immunohistochemical analyses, BRD3 was observed mainly in the nucleus of CRC cells. According to single-cell RNA sequencing in untreated CRC tissues, BRD3 was highly expressed in malignant epithelial cells, and cell cycle checkpoint-related pathways were enriched in the epithelial cells with high BRD3 expression. Spatial transcriptomic and single-cell RNA sequencing analyses of CRC tissues showed that BRD3 expression was positively associated with high p21 expression. Furthermore, overexpression of BRD3 combined with knockdown of, a driver gene in the BRD family, showed strong inhibition of CRC cells in vitro. In conclusion, we demonstrated a novel tumor suppressive role of BRD3 that inhibits tumor growth by cell cycle inhibition in part via induction of p21 expression. BRD3 activation might be a novel therapeutic approach for CRC.

摘要

溴结构域和末端结构域(BET)家族蛋白通过识别乙酰化组蛋白并募集转录因子和共激活因子到染色质,成为表观遗传基因表达的主要调控因子。因此,BET 家族蛋白已成为癌症治疗的有前途的靶点。在这项研究中,我们研究了溴结构域包含蛋白 3(BRD3)在结直肠癌(CRC)中的功能作用。使用 BRD3 敲低或过表达 CRC 细胞的体外和体内分析表明,BRD3 抑制肿瘤生长和细胞周期 G1/S 过渡,并诱导 p21 表达。对来自我们医院或癌症基因组图谱的 CRC 数据集的临床分析表明,BET 家族基因,包括 BRD3,在肿瘤组织中过度表达。在免疫组织化学分析中,BRD3 主要观察到在 CRC 细胞的核内。根据未经处理的 CRC 组织的单细胞 RNA 测序,BRD3 在恶性上皮细胞中高度表达,并且细胞周期检查点相关途径在高 BRD3 表达的上皮细胞中富集。CRC 组织的空间转录组和单细胞 RNA 测序分析表明,BRD3 表达与高 p21 表达呈正相关。此外,BRD3 的过表达与 BRD 家族的驱动基因的敲低相结合,在体外强烈抑制 CRC 细胞。总之,我们证明了 BRD3 的一种新的肿瘤抑制作用,通过诱导 p21 表达部分抑制肿瘤生长。BRD3 的激活可能是 CRC 的一种新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28f8/11145117/948d2ae23d4b/CAS-115-1866-g004.jpg

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