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作为肿瘤学中发育性治疗靶点的节点信号传导

Nodal Signaling as a Developmental Therapeutics Target in Oncology.

作者信息

Kalyan Aparna, Carneiro Benedito A, Chandra Sunandana, Kaplan Jason, Chae Young Kwang, Matsangou Maria, Hendrix Mary J C, Giles Francis

机构信息

Developmental Therapeutics Program, Division of Hematology and Oncology, Northwestern University Feinberg School of Medicine, Olson Pavilion, Chicago, Illinois.

Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, Illinois.

出版信息

Mol Cancer Ther. 2017 May;16(5):787-792. doi: 10.1158/1535-7163.MCT-16-0215.

Abstract

The tumor microenvironment is a vital feature of oncogenesis and tumor progression. There are several parallels between cancer cells and early developmental stem cells, including their plasticity and signaling mechanisms. In early fetal development, Nodal is expressed for endodermal and mesodermal differentiation. This expression has been shown reemerge in the setting of epithelial cancers, such as breast and melanoma. High Nodal expression correlates to an aggressive tumor grade in these malignancies. Nodal signal begins with its interaction with its coreceptor, Cripto-1, leading to activation of Smad2/Smad3 and ultimately downstream transcription and translation. Lefty is the natural inhibitor of Nodal and controls Nodal signaling during fetal development. However, cancer cells lack the presence of Lefty, thus leading to uncontrolled tumor growth. Given this understanding, inhibition of the Nodal pathway offers a new novel therapeutic target in oncology. .

摘要

肿瘤微环境是肿瘤发生和进展的一个重要特征。癌细胞与早期发育干细胞之间存在若干相似之处,包括它们的可塑性和信号传导机制。在胎儿早期发育过程中,Nodal表达用于内胚层和中胚层分化。这种表达已被证明在乳腺癌和黑色素瘤等上皮癌中重新出现。在这些恶性肿瘤中,高Nodal表达与侵袭性肿瘤分级相关。Nodal信号始于其与共受体Cripto-1的相互作用,导致Smad2/Smad3激活,并最终导致下游转录和翻译。Lefty是Nodal的天然抑制剂,在胎儿发育过程中控制Nodal信号传导。然而,癌细胞中缺乏Lefty,从而导致肿瘤生长不受控制。基于这一认识,抑制Nodal通路为肿瘤学提供了一个新的治疗靶点。

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