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A Case Report of a Rare Sarcomatoid Poorly Differentiated Adenocarcinoma Harboring Concurrent Mutations in the ROS1, EGFR, ARID1A, and NFKBIA Genes in the Lung
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作者 Jinlin Du Lanlan Li +3 位作者 Shiqi Song Siqin Chen yaxian yang Jian Huang 《Journal of Cancer Therapy》 2024年第5期231-237,共7页
ROS1 and EGFR are primary oncogenic drivers in non-small cell lung cancer (NSCLC) pathogenesis. However, EGFR mutations and ROS1 fusions are generally mutually exclusive in NSCLC, leading to a negligible probability o... ROS1 and EGFR are primary oncogenic drivers in non-small cell lung cancer (NSCLC) pathogenesis. However, EGFR mutations and ROS1 fusions are generally mutually exclusive in NSCLC, leading to a negligible probability of their co-occurrence. Consequently, clinical data and treatment strategies for their simultaneous presence are remarkably scarce. This report details the first recorded case of a sarcomatoid, poorly differentiated lung adenocarcinoma harboring both a ROS1 fusion and an EGFR mutation, alongside ARID1A and NFKBIA gene mutations. Moreover, this case study encompasses a review of instances featuring concurrent ROS1 and EGFR mutations. The identified genetic alterations in ROS1, EGFR, ARID1A, and NFKBIA are pivotal in the etiology of NSCLC. These mutations significantly influence disease progression and are essential for the development of personalized therapeutic approaches. Recognizing the unique genetic profiles in patients permits healthcare providers to devise customized treatment regimens that target these specific mutations, thereby enhancing patient outcomes in NSCLC. 展开更多
关键词 Non-Small Cell Lung Cancer ROS1 EGFR SARCOMATOID
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BRAF突变在非小细胞肺癌中的研究进展
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作者 邓李变 杨雅娴 黄剑 《中国肺癌杂志》 CAS CSCD 北大核心 2024年第1期73-80,共8页
鼠类肉瘤病毒癌基因同源物(V-Raf murine sarcoma viral oncogene homolog B,BRAF)突变是非小细胞肺癌(non-small cell lung cancer,NSCLC)的重要驱动基因之一。BRAF基因编码丝氨酸/苏氨酸蛋白激酶,BRAF突变通常导致其编码蛋白质的活化... 鼠类肉瘤病毒癌基因同源物(V-Raf murine sarcoma viral oncogene homolog B,BRAF)突变是非小细胞肺癌(non-small cell lung cancer,NSCLC)的重要驱动基因之一。BRAF基因编码丝氨酸/苏氨酸蛋白激酶,BRAF突变通常导致其编码蛋白质的活化,从而导致丝裂原活化蛋白激酶激酶(mitogen-activated protein kinase kinase,MEK)信号传导途径的激活。针对BRAF突变或其下游MEK靶向药物的临床应用,为BRAF突变的NSCLC提供了更为针对性及有效的治疗。然而这些方案也存在获益持续时间短、BRAF非V600突变治疗效果差、易耐药等问题,需要新的复合治疗方案来改善。本文就BRAF基因结构特点、相关信号通路、突变类型,尤其是BRAF突变和NSCLC的临床病理联系及治疗进展等方面进行综述,为临床医生选择更有效的治疗方案提供依据。 展开更多
关键词 肺肿瘤 BRAF基因 靶向治疗
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Tunable triangular and honeycomb plasma structures in dielectric barrier discharge with mesh-liquid electrodes 被引量:2
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作者 范伟丽 侯笑含 +7 位作者 田淼 高匡雅 贺亚峰 杨亚贤 刘倩 姚静锋 刘富成 袁承勋 《Plasma Science and Technology》 SCIE EI CAS CSCD 2022年第1期61-69,共9页
We demonstrate a method to generate tunable triangular and honeycomb plasma structures via dielectric barrier discharge with uniquely designed mesh-liquid electrodes.A rapid reconfiguration between the triangular latt... We demonstrate a method to generate tunable triangular and honeycomb plasma structures via dielectric barrier discharge with uniquely designed mesh-liquid electrodes.A rapid reconfiguration between the triangular lattice and honeycomb lattice has been realized.Novel structures comprised of triangular plasma elements have been observed and a robust angular reorientation of the triangular plasma elements withθ=π/3 is suggested.An active control on the geometrical shape,size and angular orientation of the plasma elements has been achieved.Moreover,the formation mechanism of different plasma structures is studied by spatial-temporal resolved measurements using a high-speed camera.The photonic band diagrams of the plasma structures are calculated by use of finite element method and two large omnidirectional band gaps have been obtained for honeycomb lattices,demonstrating that such plasma structures can be potentially used as plasma photonic crystals to manipulate the propagation of microwaves.The results may offer new strategies for engineering the band gaps and provide enlightenments on designing new types of 2D and possibly 3D metamaterials in other fields. 展开更多
关键词 dielectric barrier discharge triangular lattice honeycomb lattice photonic band diagrams plasma photonic crystals
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