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[非小细胞肺癌中KRAS突变的研究进展]

[Research Progress of KRAS Mutation in Non-small Cell Lung Cancer].

作者信息

Liu Lei, Wei Suju

机构信息

Department of Medical Oncology, Fourth Hospital of Heibei Medical Medical University, Shijiazhuang 050011, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2018 May 20;21(5):419-424. doi: 10.3779/j.issn.1009-3419.2018.05.11.

DOI:10.3779/j.issn.1009-3419.2018.05.11
PMID:29764594
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5999922/
Abstract

Lung cancer is the leading cause of cancer-related deaths worldwide. Non-small cell lung cancer (NSCLC) accounts for 80%-85% of all patients with lung cancer, the majority of patients with lung cancer at the time of diagnosis is in the advanced stage. The development of target therapy based on has changed the mode of treatment in patients with advanced NSCLC. In NSCLC, epidermal growth factor receptor mutation (EGFR) fusion with echinoderm microtubule-associated protein-like4-anaplastic lymphoma kinase (EML4-ALK) has been shown to be a powerful biomarker. It is well known that KRAS is also NSCLC one of the most common mutations in oncogenes, although more than 20 years ago KRAS mutation was found in NSCLC. At present, although there are many drugs used to treat NSCLC patients with KRAS mutation, there is no selective or specific inhibitor for the direct elimination of KRAS activity. NSCLC patients with KRAS mutation have poor responsiveness to most systemic therapy. However, individualized therapy for activated signaling pathways with targeted drugs has a good effect on the prognosis of NSCLC patients with KRAS mutation. In addition, the prognostic and predictive role of KRAS mutation in NSCLC remains unclear. In this review, we focus on the research progress of NSCLC with KRAS mutation, including molecular biology, clinicopathological features, prognosis and prediction of KRAS mutation, which will help to improve the understanding of NSCLC in KRAS mutation.
.

摘要

肺癌是全球癌症相关死亡的主要原因。非小细胞肺癌(NSCLC)占所有肺癌患者的80%-85%,大多数肺癌患者在诊断时已处于晚期。基于此的靶向治疗发展改变了晚期NSCLC患者的治疗模式。在NSCLC中,表皮生长因子受体突变(EGFR)与棘皮动物微管相关蛋白样4-间变性淋巴瘤激酶(EML4-ALK)融合已被证明是一种强大的生物标志物。众所周知,KRAS也是NSCLC中最常见的致癌基因突变之一,尽管20多年前就在NSCLC中发现了KRAS突变。目前,虽然有许多药物用于治疗KRAS突变的NSCLC患者,但尚无直接消除KRAS活性的选择性或特异性抑制剂。KRAS突变的NSCLC患者对大多数全身治疗反应较差。然而,用靶向药物对激活的信号通路进行个体化治疗对KRAS突变的NSCLC患者的预后有良好效果。此外,KRAS突变在NSCLC中的预后和预测作用仍不清楚。在本综述中,我们聚焦于KRAS突变的NSCLC的研究进展,包括分子生物学、临床病理特征、KRAS突变的预后及预测,这将有助于提高对KRAS突变的NSCLC的认识。

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KRAS mutation-induced upregulation of PD-L1 mediates immune escape in human lung adenocarcinoma.KRAS突变诱导的PD-L1上调介导人肺腺癌的免疫逃逸。
Cancer Immunol Immunother. 2017 Sep;66(9):1175-1187. doi: 10.1007/s00262-017-2005-z. Epub 2017 Apr 27.
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