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神经内分泌肿瘤中的Notch信号通路

Notch Signaling in Neuroendocrine Tumors.

作者信息

Crabtree Judy S, Singleton Ciera S, Miele Lucio

机构信息

Department of Genetics, Louisiana State University Health Sciences Center, New Orleans, LA, USA; Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA, USA.

Department of Genetics, Louisiana State University Health Sciences Center , New Orleans, LA , USA.

出版信息

Front Oncol. 2016 Apr 14;6:94. doi: 10.3389/fonc.2016.00094. eCollection 2016.

DOI:10.3389/fonc.2016.00094
PMID:27148486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4830836/
Abstract

Carcinoids and neuroendocrine tumors (NETs) are a heterogeneous group of tumors that arise from the neuroendocrine cells of the GI tract, endocrine pancreas, and the respiratory system. NETs remain significantly understudied with respect to molecular mechanisms of pathogenesis, particularly the role of cell fate signaling systems such as Notch. The abundance of literature on the Notch pathway is a testament to its complexity in different cellular environments. Notch receptors can function as oncogenes in some contexts and tumor suppressors in others. The genetic heterogeneity of NETs suggests that to fully understand the roles and the potential therapeutic implications of Notch signaling in NETs, a comprehensive analysis of Notch expression patterns and potential roles across all NET subtypes is required.

摘要

类癌和神经内分泌肿瘤(NETs)是一组异质性肿瘤,起源于胃肠道、内分泌胰腺和呼吸系统的神经内分泌细胞。就发病机制的分子机制而言,NETs仍未得到充分研究,尤其是细胞命运信号系统(如Notch)的作用。关于Notch通路的大量文献证明了其在不同细胞环境中的复杂性。Notch受体在某些情况下可作为癌基因发挥作用,而在其他情况下则可作为肿瘤抑制因子。NETs的基因异质性表明,要全面了解Notch信号在NETs中的作用及其潜在的治疗意义,需要对所有NET亚型的Notch表达模式和潜在作用进行综合分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08a/4830836/6f8b47ff3011/fonc-06-00094-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08a/4830836/0ed54e59187d/fonc-06-00094-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08a/4830836/6f8b47ff3011/fonc-06-00094-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08a/4830836/0ed54e59187d/fonc-06-00094-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08a/4830836/6f8b47ff3011/fonc-06-00094-g002.jpg

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Int J Cancer. 2016 Feb 15;138(4):927-38. doi: 10.1002/ijc.29835. Epub 2015 Sep 25.
2
A DLL3-targeted antibody-drug conjugate eradicates high-grade pulmonary neuroendocrine tumor-initiating cells in vivo.一种靶向DLL3的抗体药物偶联物可在体内根除高级别肺神经内分泌肿瘤起始细胞。
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Comprehensive genomic profiles of small cell lung cancer.
神经内分泌转化作为肺癌靶向治疗耐药的一种机制:新出现的机制及其治疗意义
Cancers (Basel). 2025 Jan 15;17(2):260. doi: 10.3390/cancers17020260.
4
Relationship between the expressions of DLL3, ASC1, TTF-1 and Ki-67: First steps of precision medicine at SCLC.DLL3、ASC1、TTF-1 和 Ki-67 的表达关系:小细胞肺癌精准医学的初探。
Oncotarget. 2024 Oct 11;15:750-763. doi: 10.18632/oncotarget.28660.
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An Overview of Altered Pathways Associated with Sensitivity to Platinum-Based Chemotherapy in Neuroendocrine Tumors: Strengths and Prospects.神经内分泌肿瘤铂类化疗敏感性相关改变途径概述:优势与前景。
Int J Mol Sci. 2024 Aug 6;25(16):8568. doi: 10.3390/ijms25168568.
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Oncogene. 2024 Sep;43(38):2885-2899. doi: 10.1038/s41388-024-03125-x. Epub 2024 Aug 18.
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