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神经调节蛋白1基因()。肺癌治疗中一个潜在的新的可靶向改变。

Neuregulin 1 Gene (). A Potentially New Targetable Alteration for the Treatment of Lung Cancer.

作者信息

Rosas Daniel, Raez Luis E, Russo Alessandro, Rolfo Christian

机构信息

The Internal Medicine Department, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.

Thoracic Oncology Program, Memorial Cancer Institute/Memorial Health Care System, Florida International University (FIU), Miami, FL 33021, USA.

出版信息

Cancers (Basel). 2021 Oct 9;13(20):5038. doi: 10.3390/cancers13205038.

Abstract

Oncogenic gene fusions are hybrid genes that result from structural DNA rearrangements, leading to unregulated cell proliferation by different mechanisms in a wide variety of cancer. This has led to the development of directed therapies to antagonize a variety of mechanisms that lead to cell growth or proliferation. Multiple oncogene fusions are currently targeted in lung cancer treatment, such as those involving and among many others. Neuregulin (NRG) gene fusion has been described in the development of normal tissue as well as in a variety of diseases, such as schizophrenia, Hirschsprung's disease, atrial fibrillation and, most recently, the development of various types of solid tumors, such as renal, gastric, pancreatic, breast, colorectal and, more recently, lung cancer. The mechanism for this is that the chimeric ligand leads to aberrant activation of signaling via PI3K-AKT and MAPK cellular cascades, leading to cell division and proliferation. Details regarding the incidence of these gene rearrangements are lacking. Limited case reports and case series have evaluated their clinicopathologic features and prognostic significance in the lung cancer population. Taking this into account, could become a targetable alteration in selected patients. This review highlights how the knowledge of new molecular mechanisms of fusion may help in gaining new insights into the molecular status of lung cancer patients and unveil a novel targetable molecular marker.

摘要

致癌基因融合是由DNA结构重排产生的杂交基因,通过多种机制导致多种癌症中细胞增殖失控。这促使了定向疗法的发展,以对抗导致细胞生长或增殖的多种机制。目前在肺癌治疗中靶向多种致癌基因融合,例如涉及众多其他基因的融合。神经调节蛋白(NRG)基因融合已在正常组织发育以及多种疾病中被描述,如精神分裂症、先天性巨结肠、心房颤动,以及最近在各种实体瘤的发生中,如肾癌、胃癌、胰腺癌、乳腺癌、结直肠癌,以及最近的肺癌。其机制是嵌合配体通过PI3K-AKT和MAPK细胞级联导致 信号异常激活,从而导致细胞分裂和增殖。缺乏关于这些基因重排发生率的详细信息。有限的病例报告和病例系列评估了它们在肺癌人群中的临床病理特征和预后意义。考虑到这一点, 在特定患者中可能成为一个可靶向的改变。本综述强调了对 融合新分子机制的了解如何有助于深入了解肺癌患者的分子状态,并揭示一种新的可靶向分子标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c8c/8534274/bf40e57f8cec/cancers-13-05038-g001.jpg

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