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人类结直肠癌的表观基因组景观揭示了由 YAP/TAZ 协调的异常泛癌增强子核心。

Epigenomic landscape of human colorectal cancer unveils an aberrant core of pan-cancer enhancers orchestrated by YAP/TAZ.

机构信息

IFOM, the FIRC Institute of Molecular Oncology, Milan, Italy.

Istituto Nazionale Genetica Molecolare INGM 'Romeo ed Enrica Invernizzi', Milan, Italy.

出版信息

Nat Commun. 2021 Apr 20;12(1):2340. doi: 10.1038/s41467-021-22544-y.

Abstract

Cancer is characterized by pervasive epigenetic alterations with enhancer dysfunction orchestrating the aberrant cancer transcriptional programs and transcriptional dependencies. Here, we epigenetically characterize human colorectal cancer (CRC) using de novo chromatin state discovery on a library of different patient-derived organoids. By exploring this resource, we unveil a tumor-specific deregulated enhancerome that is cancer cell-intrinsic and independent of interpatient heterogeneity. We show that the transcriptional coactivators YAP/TAZ act as key regulators of the conserved CRC gained enhancers. The same YAP/TAZ-bound enhancers display active chromatin profiles across diverse human tumors, highlighting a pan-cancer epigenetic rewiring which at single-cell level distinguishes malignant from normal cell populations. YAP/TAZ inhibition in established tumor organoids causes extensive cell death unveiling their essential role in tumor maintenance. This work indicates a common layer of YAP/TAZ-fueled enhancer reprogramming that is key for the cancer cell state and can be exploited for the development of improved therapeutic avenues.

摘要

癌症的特征是普遍存在的表观遗传改变,增强子功能障碍协调异常的癌症转录程序和转录依赖性。在这里,我们使用不同患者来源的类器官文库中的从头染色质状态发现来对人结直肠癌(CRC)进行表观遗传表征。通过探索这个资源,我们揭示了一个肿瘤特异性的失调增强子组,它是肿瘤细胞内在的,独立于患者间异质性的。我们表明,转录共激活因子 YAP/TAZ 是保守的 CRC 获得增强子的关键调节因子。相同的 YAP/TAZ 结合增强子在不同的人类肿瘤中显示出活跃的染色质特征,突出了一种泛癌症的表观遗传重编程,在单细胞水平上区分了恶性和正常细胞群体。在已建立的肿瘤类器官中抑制 YAP/TAZ 会导致广泛的细胞死亡,揭示了它们在肿瘤维持中的关键作用。这项工作表明,YAP/TAZ 驱动的增强子重编程是癌症细胞状态的关键共同层,可用于开发改进的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2c0/8058065/b84b6e9a5c3e/41467_2021_22544_Fig1_HTML.jpg

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