Clinical features and molecular genetics associated with brain metastasis in suspected early-stage non-small cell lung cancer

被引:3
作者
Kim, Kangjoon [1 ,3 ]
Lee, Jibeom [2 ]
Lee, Jeong-Yun [2 ]
Yong, Seung Hyun [1 ]
Kim, Eun Young [1 ]
Jung, Ji Ye [1 ]
Kang, Young Ae [1 ]
Park, Moo Suk [1 ]
Kim, Young Sam [1 ]
Oh, Chang-Myung [2 ]
Lee, Sang Hoon [1 ]
机构
[1] Yonsei Univ, Severance Hosp, Dept Internal Med, Div Pulm & Crit Care Med,Coll Med, Seoul, South Korea
[2] Gwangju Inst Sci & Technol, Dept Biomed Sci & Engn, Gwangju, South Korea
[3] Chung Ang Univ, Coll Med, Dept Internal Medicine, Gwangmyeong Hosp,Div Pulm Allergy & Crit Care Med, Gwangmyeong, South Korea
基金
新加坡国家研究基金会;
关键词
early stage lung cancer; non-small cell lung cancer; brain metastasis; magnetic resonance imaging; UNC79; SCREENING TRIAL; EXPRESSION; PROGNOSIS; DIAGNOSIS; PROTEINS; SURVIVAL; INTACT;
D O I
10.3389/fonc.2023.1148475
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
IntroductionRegarding whether brain magnetic resonance imaging (MRI) should be routine in patients with suspected early-stage lung cancer, guideline recommendations are inconsistent. Therefore, we performed this study to evaluate the incidence of and risk factors for brain metastasis (BM) in patients with suspected early-stage non-small-cell lung cancer (NSCLC). MethodsA review of the medical charts of consecutive NSCLC patients diagnosed between January 2006 and May 2020 was performed. We identified 1,382 NSCLC patients with clinical staging of T1/2aN0M0 (excluding BM), and investigated the incidence, clinical predictors, and prognosis of BM in the cohort. We also performed RNA-sequencing differential expression analysis using transcriptome of 8 patients, using DESeq2 package (version 1.32.0) with R (version 4.1.0). ResultsAmong 1,382 patients, nine hundred forty-nine patients (68.7%) underwent brain MRI during staging, and 34 patients (3.6%) were shown to have BM. Firth's bias-reduced logistic regression showed that tumor size (OR 1.056; 95% CI 1.009-1.106, p=0.018) was the only predictor of BM, and pathologic type was not a predictor of BM in our cohort (p>0.05). The median overall survival for patients with brain metastasis was 5.5 years, which is better than previously reported in the literature. RNA-sequencing differential expression analysis revealed the top 10 significantly upregulated genes and top 10 significantly downregulated genes. Among the genes involved in BM, Unc-79 homolog, non-selective sodium leak channel (NALCN) channel complex subunit (UNC79) was the most highly expressed gene in the lung adenocarcinoma tissues from the BM group, and an in vitro assay using A549 cells revealed that the NALCN inhibitor suppressed lung cancer cell proliferation and migration. ConclusionsGiven the incidence and favorable outcome of BM in patients with suspected early-stage NSCLC, selective screening with brain MRI may be considered, especially in patients with high-risk features.
引用
收藏
页数:12
相关论文
共 54 条
[31]   Survival and neurologic outcomes in a randomized trial of motexafin gadolinium and whole-brain radiation therapy in brain metastases [J].
Mehta, MP ;
Rodrigus, P ;
Terhaard, CHJ ;
Rao, A ;
Suh, J ;
Roa, W ;
Soukami, L ;
Bezjak, A ;
Leibenhaut, M ;
Komaki, R ;
Schultz, C ;
Timmerman, R ;
Curran, W ;
Smith, J ;
Phan, SC ;
Miller, RA ;
Renschler, MF .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (13) :2529-2536
[32]   Risk of brain metastases in T1-3N0 NSCLC: a population-based analysis [J].
Milano, Michael T. ;
Bates, James E. ;
Budnik, Justin ;
Qiu, Haoming ;
Hardy, Sara ;
Cummings, Michael A. ;
Baumgart, Megan A. ;
Maggiore, Ronald J. ;
Mulford, Deborah A. ;
Usuki, Kenneth Y. .
LUNG CANCER MANAGEMENT, 2020, 9 (01)
[33]  
Nagano Makoto, 2012, Int J Cell Biol, V2012, P310616, DOI 10.1155/2012/310616
[34]   Identification of key modules and hub genes for small-cell lung carcinoma and large-cell neuroendocrine lung carcinoma by weighted gene co-expression network analysis of clinical tissue-proteomes [J].
Nakamura, Haruhiko ;
Fujii, Kiyonaga ;
Gupta, Vipul ;
Hata, Hiroko ;
Koizumu, Hirotaka ;
Hoshikawa, Masahiro ;
Naruki, Saeko ;
Miyata, Yuka ;
Takahashi, Ikuya ;
Miyazawa, Tomoyuki ;
Sakai, Hiroki ;
Tsumoto, Kouhei ;
Takagi, Masayuki ;
Saji, Hisashi ;
Nishimura, Toshihide .
PLOS ONE, 2019, 14 (06)
[35]  
Network NCC, NONSM CELL LUNG CANC
[36]   Twist1-induced epithelial-mesenchymal transition according to microsatellite instability status in colon cancer cells [J].
Oh, Bo Young ;
Kim, So-Young ;
Lee, Yeo Song ;
Hong, Hye Kyung ;
Kim, Tae Won ;
Kim, Seok Hyung ;
Lee, Woo Yong ;
Cho, Yong Beom .
ONCOTARGET, 2016, 7 (35) :57066-57076
[37]   The MIntAct project-IntAct as a common curation platform for 11 molecular interaction databases [J].
Orchard, Sandra ;
Ammari, Mais ;
Aranda, Bruno ;
Breuza, Lionel ;
Briganti, Leonardo ;
Broackes-Carter, Fiona ;
Campbell, Nancy H. ;
Chavali, Gayatri ;
Chen, Carol ;
del-Toro, Noemi ;
Duesbury, Margaret ;
Dumousseau, Marine ;
Galeota, Eugenia ;
Hinz, Ursula ;
Iannuccelli, Marta ;
Jagannathan, Sruthi ;
Jimenez, Rafael ;
Khadake, Jyoti ;
Lagreid, Astrid ;
Licata, Luana ;
Lovering, Ruth C. ;
Meldal, Birgit ;
Melidoni, Anna N. ;
Milagros, Mila ;
Peluso, Daniele ;
Perfetto, Livia ;
Porras, Pablo ;
Raghunath, Arathi ;
Ricard-Blum, Sylvie ;
Roechert, Bernd ;
Stutz, Andre ;
Tognolli, Michael ;
van Roey, Kim ;
Cesareni, Gianni ;
Hermjakob, Henning .
NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) :D358-D363
[38]   Promotion of Cancer Cell Invasiveness and Metastasis Emergence Caused by Olfactory Receptor Stimulation [J].
Sanz, Guenhael ;
Leray, Isabelle ;
Dewaele, Aurelie ;
Sobilo, Julien ;
Lerondel, Stephanie ;
Bouet, Stephan ;
Grebert, Denise ;
Monnerie, Regine ;
Pajot-Augy, Edith ;
Mir, Lluis M. .
PLOS ONE, 2014, 9 (01)
[39]   Cytoscape: A software environment for integrated models of biomolecular interaction networks [J].
Shannon, P ;
Markiel, A ;
Ozier, O ;
Baliga, NS ;
Wang, JT ;
Ramage, D ;
Amin, N ;
Schwikowski, B ;
Ideker, T .
GENOME RESEARCH, 2003, 13 (11) :2498-2504
[40]   Mechanisms and Functions of Chemerin in Cancer: Potential Roles in Therapeutic Intervention [J].
Shin, Woo Jae ;
Zabel, Brian A. ;
Pachynski, Russell K. .
FRONTIERS IN IMMUNOLOGY, 2018, 9