scholarly journals Chemotherapeutic Agents Increase PD-L1 Expression in A549 Lung Cancer Cell Line

Author(s):  
Haniye Ajdary ◽  
Sahar Safaei ◽  
Shahryar Hashemzadeh ◽  
Tohid Kazemi ◽  
Dariush Shanehbandi ◽  
...  

Abstract Introduction: With the highest mortality rate, lung cancer is one of the most prevalent malignancies worldwide. Increasing PD-L1 expression is one of the mechanisms of ineffective anti-tumor response and immune evasion, which causes poor prognosis and survival rate. Chemotherapy has its own limitations such as drug resistance and the escape of cancer cells from the immune system. The current research aimed to assess the effects of common chemotherapy agents used in lung cancer on PD-L1 expression in tumor cells in order to help for selecting appropriate treatment regimens to increase patient survival. Methods First, A549 cells were cultured, and the expression of PD-L1 on this cell line was measured by qRT-PCR. Then, the viability of cancer cells was examined by MTT test. PD-L1 gene expression was measured by qRT-PCR in A549 cell line, after treatment with chemotherapy agents. Results PD-L1 gene expression was increased after 24 and 48 hours after treatment with cisplatin, docetaxel, paclitaxel and carboplatin. The IC50 of the mentioned drugs 24 hours after treatment were evaluated 27, 38.79, 18.66, and 54.17 µg/ml respectively. Conclusion The current study shows that PD-L1 expression increases in response to carboplatin, docetaxel, cisplatin, and paclitaxel in A549 cell line. This indicates that chemotherapy agents cause immune evasion by increasing PD-L1 expression on cancer cells, which makes these cells resistant to the immune system. The results also showed that carboplatin, docetaxel, cisplatin, and paclitaxel at 48 hours after treatment had a greater effect on increasing PD-L1 expression than 24 hours after treatment.

RSC Advances ◽  
2016 ◽  
Vol 6 (40) ◽  
pp. 33631-33635 ◽  
Author(s):  
A. Sofia Silva ◽  
Marta C. Silva ◽  
Sónia P. Miguel ◽  
Vasco D. B. Bonifácio ◽  
Ilídio J. Correia ◽  
...  

Gold nanoparticles (GNPs) were POxylated with fluorescent oligomers, synthesized in supercritical CO2, and conjugated with a laminin fragment. Particle design strongly impacts on probes uptake by the A549 cell line.


2018 ◽  
Vol 14 (5) ◽  
pp. 1822
Author(s):  
Wai-Kin Yu ◽  
Yuen-San Chan ◽  
Weimao Wang ◽  
Chi-chun Fong ◽  
Tak-Chun Yip ◽  
...  

2019 ◽  
Author(s):  
Sorush Niknamian

Currently, epigenetic changes are considered to be one of the most important factors in the incidence of cancer and its metastasis to various tissues. It has been shown that CD44v6 and Nm23-H1 genes play a crucial role in the metastasis of various cancers. However, no study has been done on the effect of epigenetic factors on the expression of CD44v6 and Nm23-H1 genes in the lung cancer cell line, A549.Therefore, the present study investigated the role of a histone deacetylase inhibitor, valproic acid, on the expression of CD44v6 and Nm23-H1 genes and proteins in the A549 cell line. In this study, the A549 cell line was treated with valproic acid at concentrations of 2.2 mM, 4.5 mM, and 9 mM. We then investigated the expression of CD44v6 and Nm23-H1 genes and proteins, as well as the expression of MMP-2 and MMP-9 genes and caspase-3 activity. The results showed that valproic acid significantly decreased the expression of CD44v6 gene and protein and MMP-2 and MMP-9 genes, but increased the expression of Nm23H1 gene and protein and the activity of caspase-3 (p˂ 0.05). Our results showed that histone deacetylases affected the expression of CD44v6, Nm23-H1, MMP-2, and MMP-9, which are involved in metastasis. Therefore, the use of histone deacetylase inhibitors can be effective in the suppression of metastases and the treatment of lung cancer.


2019 ◽  
Vol 32 (2) ◽  
pp. 297-302 ◽  
Author(s):  
Bharath Samannan ◽  
Jothi Selvam ◽  
Jeyabalan Thavasikani

A novel hybrid composite, namely {[VIV+PMo11O40]⊂[β-CD]} which shows the high percent of apoptosis of MTT assay of A549 cell line (lung cancer) in different concentrations. The composite has been characterized using techniques such as FT-IR, EPR, SEM, EDS and X-ray diffraction. The anticancer (lung cancer A549 cell line) was investigated using direct microscopic observations for drug treated cell line and IC50 value of 1.93. The apoptosis of 45.37 % cell death in cell line of minimum concentration (3.12 μg/mL) shows the good viability of β-CD-POM against lung cancer A549 cell line.


2016 ◽  
Vol 13 (2) ◽  
pp. 1019-1023 ◽  
Author(s):  
Ping Mao ◽  
Ershao Zhang ◽  
Yang Chen ◽  
Likun Liu ◽  
Daqing Rong ◽  
...  

2020 ◽  
Vol 21 (1) ◽  
pp. 49-54
Author(s):  
Parichart Boueroy ◽  
Thidarut Boonmars ◽  
Somdej Kanokmedhakul ◽  
Sorujsiri Chareonsudjai ◽  
Ratsami Lekphrom ◽  
...  

2017 ◽  
Vol 11 (6) ◽  
pp. 578-583
Author(s):  
Samer Hasan Hussein-Al-Ali ◽  
Mothanna Al-Qubaisi ◽  
Abdullah Rasedee ◽  
Mohd Zobir Hussein

Sign in / Sign up

Export Citation Format

Share Document