P-406 Prognostic significance of Bax and Fas ligand in erionite andasbestos induced Turkish malignant pleural mesothelioma

Lung Cancer ◽  
2005 ◽  
Vol 49 ◽  
pp. S222
Author(s):  
N. Kokturk ◽  
S. Emri ◽  
P. Firat ◽  
H. Akay ◽  
C. Kadilar ◽  
...  
Lung Cancer ◽  
2005 ◽  
Vol 50 (2) ◽  
pp. 189-198 ◽  
Author(s):  
Nurdan Kokturk ◽  
Pinar Firat ◽  
Hadi Akay ◽  
Cem Kadilar ◽  
Can Ozturk ◽  
...  

Oncotarget ◽  
2017 ◽  
Vol 8 (28) ◽  
pp. 46425-46435 ◽  
Author(s):  
Long Tian ◽  
Rujun Zeng ◽  
Xin Wang ◽  
Cheng Shen ◽  
Yutian Lai ◽  
...  

2014 ◽  
Vol 32 (15_suppl) ◽  
pp. 7580-7580
Author(s):  
Steven Chuan-Hao Kao ◽  
Michaela Kirschner ◽  
Mark P. Molloy ◽  
Stephen John Clarke ◽  
Sjaak A. Burgers ◽  
...  

Lung Cancer ◽  
2015 ◽  
Vol 90 (1) ◽  
pp. 111-117 ◽  
Author(s):  
Tomoko Yamagishi ◽  
Nobukazu Fujimoto ◽  
Hideyuki Nishi ◽  
Yosuke Miyamoto ◽  
Naofumi Hara ◽  
...  

2020 ◽  
Vol 12 ◽  
pp. 175883592096236
Author(s):  
Liu Jin ◽  
Weiling Gu ◽  
Xueqin Li ◽  
Liang Xie ◽  
Linhong Wang ◽  
...  

Background: The prognostic value of programmed death-ligand 1 (PD-L1) expression in patients with malignant pleural mesothelioma (MPM) has been controversial according to previous investigations. Therefore, we conducted a meta-analysis to assess the potential prognostic significance of PD-L1 expression in MPM. Methods: PubMed, Embase, Web of Science, Scopus, and the Cochrane Library were thoroughly searched for relevant original articles published before 9 April 2020. The pooled hazard ratios (HRs) and 95% confidence intervals (CIs) of overall survival (OS) and progression-free survival (PFS) were calculated. The results of the meta-analysis were verified using The Cancer Genome Atlas (TCGA) dataset. Results: In total 16 studies were included in our meta-analysis. A high PD-L1 expression was associated with a poor OS (HR = 1.53, 95% CI = 1.28–1.83, p < 0.001), but not a grave PFS (HR = 1.07, 95% CI = 0.82–1.39, p = 0.643) in MPM. Furthermore, the PD-L1 expression correlated with the sarcomatoid + biphasic type of MPM (odds ratio = 4.32, 95% CI = 2.16–8.64, p < 0.001). TCGA data indicated that PD-L1 was a significant prognostic factor for OS (HR = 2.069, 95% CI = 1.136–3.769, p = 0.0175), but not for PFS (HR = 1.205, 95% CI = 0.572–2.539, p = 0.624), which was in accordance with the results of the meta-analysis. Conclusion: A high PD-L1 expression is a significant prognostic factor for poor OS of patients with MPM. We therefore suggest that PD-L1 expression levels can be used to predict the clinical outcomes of patients with MPM in the future.


2017 ◽  
Author(s):  
Ajay Dhakal ◽  
Saraswati Pokharel ◽  
Katy Wang ◽  
Todd Demmy ◽  
Chukwumere E. Nwogu ◽  
...  

Cells ◽  
2019 ◽  
Vol 8 (9) ◽  
pp. 1091 ◽  
Author(s):  
Gregor Vlacic ◽  
Mir A. Hoda ◽  
Thomas Klikovits ◽  
Katharina Sinn ◽  
Elisabeth Gschwandtner ◽  
...  

Malignant pleural mesothelioma (MPM) is a devastating malignancy with limited therapeutic options. Fibroblast growth factor receptors (FGFR) and their ligands were shown to contribute to MPM aggressiveness and it was suggested that subgroups of MPM patients could benefit from FGFR-targeted inhibitors. In the current investigation, we determined the expression of all four FGFRs (FGFR1–FGFR4) by immunohistochemistry in tissue samples from 94 MPM patients. From 13 of these patients, we were able to establish stable cell lines, which were subjected to FGFR1–4 staining, transcript analysis by quantitative RT-PCR, and treatment with the FGFR inhibitor infigratinib. While FGFR1 and FGFR2 were widely expressed in MPM tissue and cell lines, FGFR3 and FGFR4 showed more restricted expression. FGFR1 and FGFR2 showed no correlation with clinicopathologic data or patient survival, but presence of FGFR3 in 42% and of FGFR4 in 7% of patients correlated with shorter overall survival. Immunostaining in cell lines was more homogenous than in the corresponding tissue samples. Neither transcript nor protein expression of FGFR1–4 correlated with response to infigratinib treatment in MPM cell lines. We conclude that FGFR3 and FGFR4, but not FGFR1 or FGFR2, have prognostic significance in MPM and that FGFR expression is not sufficient to predict FGFR inhibitor response in MPM cell lines.


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