E-cadherin expression in the tumor microenvironment of advanced epidermal growth factor receptor-mutant lung adenocarcinoma and the association with prognosis

被引:6
|
作者
Chang, Yu-Ping [1 ]
Huang, Gong-Kai [2 ,3 ]
Chen, Yung-Che [1 ,4 ]
Huang, Kuo-Tung [1 ]
Chen, Yu-Mu [1 ]
Lin, Chiung-Yu [1 ]
Huang, Chao-Cheng [2 ,5 ]
Lin, Meng-Chih [1 ]
Wang, Chin-Chou [1 ,4 ,6 ]
机构
[1] Chang Gung Univ, Kaohsiung Chang Gung Mem Hosp, Dept Internal Med,Coll Med, Div Pulm & Crit Care Med, Kaohsiung, Taiwan
[2] Chang Gung Univ, Kaohsiung Chang Gung Mem Hosp, Dept Pathol, Coll Med, Kaohsiung, Taiwan
[3] Chang Gung Univ, Kaohsiung Chang Gung Mem Hosp, Dept Lab Med, Coll Med, Kaohsiung, Taiwan
[4] Chang Gung Univ, Kaohsiung Chang Gung Mem Hosp, Dept Resp Therapy, Coll Med, Kaohsiung, Taiwan
[5] Chang Gung Univ, Kaohsiung Chang Gung Mem Hosp, Dept Pathol,Coll Med, Biobank & Tissue Bank, Kaohsiung, Taiwan
[6] Chang Gung Univ Sci & Technol, Dept Resp Care, Chiayi, Taiwan
关键词
Adenocarcinoma; E-cadherin; Epidermal growth factor receptor (EGFR); Lung cancer; Programmed death-ligand 1 (PD-L1); Tumor-infiltrating lymphocytes; Vimentin; TO-MESENCHYMAL TRANSITION; HIGH PD-L1 EXPRESSION; BRAIN METASTASES; EGFR MUTATIONS; BETA-CATENIN; CANCER; MOLECULES; SURVIVAL; IMPACT; CHEMOTHERAPY;
D O I
10.1186/s12885-023-10980-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThe expression of programmed death-ligand 1 (PD-L1), tumor-infiltrating lymphocytes (TILs), E-cadherin, and vimentin in lung cancer tumor microenvironment is known to impact patient survival or response to therapy. The expression of these biomarkers may also differ between primary lung tumors and brain metastatic tumors. In this study, we investigated the interaction between these biomarkers in lung tumors with or without concomitant brain metastasis and the interaction with paired brain metastatic tumors.MethodsThe study included 48 patients with stage IV epidermal growth factor receptor (EGFR)-mutant lung adenocarcinoma. Sixteen of the forty-eight patients were diagnosed with brain metastasis, while the remaining thirty-two were not. All sixteen patients with brain metastasis had brain tumors. The expression of PD-L1, TILs (CD8(+) T lymphocytes and FOXP3(+) regulatory T lymphocytes), E-cadherin, and vimentin were evaluated using immunohistochemical (IHC) staining.ResultsPatients with brain metastasis exhibited a higher frequency of exon 19 deletion and uncommon EGFR mutations, a higher lung tumor vimentin score, worse progression-free survival (PFS), and overall survival (OS) than patients without brain metastasis. IHC staining showed no difference between paired lung and brain tumors. Patients with low PD-L1 expression had better PFS and OS. After multivariate analysis, higher body mass index, the presence of brain metastasis, bone metastasis, and uncommon EGFR mutations were correlated with worse PFS, while the presence of brain metastasis and high lung tumor E-cadherin score was associated with worse OS.ConclusionsIn patients with stage IV EGFR-mutant lung adenocarcinoma, high E-cadherin expression in the lung tumor might be associated with worse OS. Vimentin expression in the lung tumor was positively related to the risk of brain metastasis.
引用
收藏
页数:11
相关论文
共 50 条
  • [21] Expression of calcium sensing receptor and E-cadherin correlated with survival of lung adenocarcinoma
    Wen, Liyuan
    Sun, Lichun
    Xi, Yuhui
    Chen, Xuesong
    Xing, Ying
    Sun, Weiling
    Meng, Qingwei
    Cai, Li
    THORACIC CANCER, 2015, 6 (06) : 754 - 760
  • [22] Expression and tyrosine phosphorylation of E-cadherin, β- and γ-catenin, and epidermal growth factor receptor in cervical cancer cells
    Moon, HS
    Choi, EA
    Park, HY
    Choi, JY
    Chung, HW
    Kim, JI
    Park, WI
    GYNECOLOGIC ONCOLOGY, 2001, 81 (03) : 355 - 359
  • [23] Infections in Patients with Advanced-stage Epidermal Growth Factor Receptor-mutant Lung Cancer e a Post-hoc Analysis of a Randomised Trial
    Sahu, H.
    Patil, V. M.
    Menon, N.
    Singh, A. K.
    Biswas, S.
    Janu, A.
    Chakraborty, N.
    Prabhash, K.
    Noronha, V.
    CLINICAL ONCOLOGY, 2023, 35 (12) : 811 - 812
  • [24] Highly Active Antitumor Therapy (HAATT) for Epidermal Growth Factor Receptor-Mutant Lung Cancer
    Chmielecki, Juliann
    Pao, William
    CLINICAL CANCER RESEARCH, 2010, 16 (22) : 5371 - 5373
  • [25] IMMUNOHISTOCHEMICAL EVALUATION OF E-CADHERIN AND EPIDERMAL GROWTH-FACTOR RECEPTOR IN NONSMALL CELL LUNG-CANCER
    SORSCHER, SM
    RUSSACK, V
    GRAZIANO, S
    CAGLE, M
    FERAMISCO, JR
    GREEN, MR
    MODERN PATHOLOGY, 1995, 8 (04) : 450 - 455
  • [26] Association of Serum Epidermal Growth Factor Receptor (EGFR) Expression with Treatment Response and Survival in Patients with Advanced Adenocarcinoma Lung
    Mohan, A.
    Masroor, M.
    Ansari, A.
    Saxena, A.
    Luthra, K.
    Jain, D.
    Pandey, R.
    Kumar, R.
    Khilnani, G. C.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2018, 197
  • [27] Distinct E-cadherin signaling complexes regulate epidermal growth factor receptor and cell growth
    Hein, PW
    Kinch, MS
    MOLECULAR BIOLOGY OF THE CELL, 1998, 9 : 49A - 49A
  • [28] Safety and Success of Repeat Lung Needle Biopsies in Patients with Epidermal Growth Factor Receptor-Mutant Lung Cancer
    Fintelmann, Florian J.
    Troschel, Fabian M.
    Kuklinski, Martin W.
    McDermott, Shaunagh
    Petranovic, Milena
    Digumarthy, Subba R.
    Sharma, Amita
    Troschel, Amelie S.
    Price, Melissa C.
    Hariri, Lida P.
    Gilman, Matthew D.
    Shepard, Joanne O.
    Sequist, Lecia V.
    Piotrowska, Zofia
    ONCOLOGIST, 2019, 24 (12): : 1570 - 1576
  • [29] EPIDERMAL GROWTH FACTOR RECEPTOR (EGFR) MUTATIONS IN ADVANCED LUNG ADENOCARCINOMA
    Chai, Chee Shee
    Liam, Chong-Kin
    RESPIROLOGY, 2015, 20 : 89 - 89
  • [30] Soluble E-cadherin promotes cell survival by activating epidermal growth factor receptor
    Inge, Landon J.
    Barwe, Sonali P.
    D'Ambrosio, Julia
    Gopal, Jegan
    Lu, Kan
    Ryazantsev, Sergey
    Rajasekaran, Sigrid A.
    Rajasekaran, Ayyappan K.
    EXPERIMENTAL CELL RESEARCH, 2011, 317 (06) : 838 - 848