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肺非小细胞癌淋巴结转移的分子特征反映了淋巴结转移机制

Molecular Features in Lymphatic Metastases Reflect the Metastasis Mechanism of Lymph Nodes With Non-Small-Cell Lung Cancers.

作者信息

Guo Nannan, Chen Yuanyuan, Jing Zhongying, Liu Siyao, Su Junyan, Li Ruilin, Duan Xiaohong, Chen Zhigong, Chen Ping, Yin Rongjiang, Li Shaojun, Tang Jian

机构信息

Department of Thoracic Surgery, Fourth Medical Center of PLA General Hospital, Beijing, China.

Department of Ultrasound, Fourth Medical Center of PLA General Hospital, Beijing, China.

出版信息

Front Bioeng Biotechnol. 2022 Jul 18;10:909388. doi: 10.3389/fbioe.2022.909388. eCollection 2022.

Abstract

Lymphatic metastasis influences clinical treatment and prognosis of patients with non-small-cell lung cancer (NSCLC). There is an urgency to understand the molecular features and mechanisms of lymph node metastasis. We analyzed the molecular features on pairs of the primary tumor and lymphatic metastasis tissue samples from 15 NSCLC patients using targeted next-generation sequencing. The potential metastasis-related genes were screened from our cohort based on cancer cell fraction. After filtering with gene functions, candidate metastasis-related events were validated in the MSK cohort with Fisher's exact test. The molecular signature and tumor mutational burden were similar in paired samples, and the average mutational concordance was 42.0% ± 28.9%. Its metastatic mechanism is potentially a linear progression based on the metastatic seeding theory. Furthermore, mutated ataxia telangiectasia mutated and Rad3-related () and tet methylcytosine dioxygenase 2 () genes were significantly enriched in lymphatic metastases ( ≤ 0.05). Alterations in these two genes could be considered metastasis-related driving events. Mutated and might play an active role in the metastasis of lymph nodes with NSCLC. More case enrollment and long-term follow-up will further verify the clinical significance of these two genes.

摘要

淋巴转移影响非小细胞肺癌(NSCLC)患者的临床治疗和预后。了解淋巴结转移的分子特征和机制迫在眉睫。我们使用靶向二代测序分析了15例NSCLC患者的原发肿瘤和淋巴转移组织样本对的分子特征。基于癌细胞分数从我们的队列中筛选潜在的转移相关基因。经基因功能筛选后,用Fisher精确检验在MSK队列中验证候选转移相关事件。配对样本中的分子特征和肿瘤突变负荷相似,平均突变一致性为42.0%±28.9%。基于转移播种理论,其转移机制可能是线性进展。此外,共济失调毛细血管扩张突变和Rad3相关蛋白()以及四甲基胞嘧啶双加氧酶2()基因的突变在淋巴转移中显著富集(≤0.05)。这两个基因的改变可被视为转移相关驱动事件。突变的和可能在NSCLC淋巴结转移中发挥积极作用。更多病例入组和长期随访将进一步验证这两个基因的临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a54/9341247/ec5de4273089/fbioe-10-909388-g001.jpg

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