NRG/ErbB signaling: on the trail of a molecular fingerprint in mucinous carcinoma.

IF 4.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Domenico Trombetta, Federico Pio Fabrizio, Massimo Di Maio, Paola Parente, Laura Melocchi, Maurizio Martini, Angelo Sparaneo, Tiziana Pia Latiano, Paolo Graziano, Giulio Rossi, Lucia Anna Muscarella
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引用次数: 0

Abstract

Introduction: Human neuregulins (NRG) are small epidermal growth factor ligands, involved inthe activation of ErbBs receptors. Among genomic aberrations, the NRG fusionsare one of the most intriguing genetic markers reported in the latest years,due to their agnostic and potentially predictive features. Mucinous carcinomashowed a higher rate of mutations in downstream effectors of NRG/ErbBactivation, thus suggesting that RAS/MAPK and PIK3K/AKT pathway are involved inmucinous phenotype development and aggressiveness.

Areacovered: Epidemiological data on the spectrum ofall NRG/ErbBs and downstream effectors alterations in mucinous carcinoma of digestivetract, ovary, lung, and pancreato-biliary tract, as well as their correlationwith respective immunological and molecular background are discussed. Peer-reviewedpublications on high-quality international from PubMed and data from scientificofficial sites were used to update the current literature.

Expertopinion: Recent scientific advances highlightthe predictive and prognostic role of the NRGs/ErbBs network deregulation incancer; anyhow its role is not well investigated in solid tumors with mucinousfeatures. Although the mucin-rich cancers have a considerably greater rate ofmutations in therapeutically critical pathways than non-mucinous ones, commonmucinous pathways have not yet been found.

NRG/ErbB信号:黏液癌的分子指纹图谱。
人神经调节因子(NRG)是一种小的表皮生长因子配体,参与erbb受体的激活。在基因组畸变中,NRG融合是近年来报道的最有趣的遗传标记之一,因为它们具有不可知论和潜在的预测性特征。在粘液癌中,NRG/ erbb激活的下游效应物的突变率更高,这表明RAS/MAPK和PIK3K/AKT通路参与了粘液表型的发展和侵袭性。涵盖领域:本文讨论了消化道、卵巢、肺和胰胆道黏液癌中所有NRG/ erbb和下游效应物谱变化的流行病学数据,以及它们与各自免疫学和分子背景的相关性。来自PubMed的同行评议的高质量国际出版物和来自科学官方网站的数据被用来更新当前的文献。观点:最近的科学进展强调了NRGs/ErbBs网络解除管制对癌症的预测和预后作用;然而,它在具有黏液特征的实体瘤中的作用尚未得到很好的研究。尽管富含黏液蛋白的癌症在治疗关键途径上的突变率比非黏液蛋白的癌症高得多,但尚未发现常见的黏液途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.90
自引率
1.70%
发文量
58
审稿时长
3 months
期刊介绍: The journal evaluates molecules, signalling pathways, receptors and other therapeutic targets and their potential as candidates for drug development. Articles in this journal focus on the molecular level and early preclinical studies. Articles should not include clinical information including specific drugs and clinical trials. The Editors welcome: Reviews covering novel disease targets at the molecular level and information on early preclinical studies and their implications for future drug development. Articles should not include clinical information including specific drugs and clinical trials. Original research papers reporting results of target selection and validation studies and basic mechanism of action studies for investigative and marketed drugs. The audience consists of scientists, managers and decision makers in the pharmaceutical industry, academic researchers working in the field of molecular medicine and others closely involved in R&D.
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