Induction of Human-Lung-Cancer-A549-Cell Apoptosis by 4-Hydroperoxy-2-decenoic Acid Ethyl Ester through Intracellular ROS Accumulation and the Induction of Proapoptotic CHOP Expression

2018 ◽  
Vol 66 (41) ◽  
pp. 10741-10747 ◽  
Author(s):  
Tetsuro Kamiya ◽  
Momoko Watanabe ◽  
Hirokazu Hara ◽  
Yukari Mitsugi ◽  
Eiji Yamaguchi ◽  
...  
2003 ◽  
Vol 50 (6) ◽  
pp. 771-781 ◽  
Author(s):  
Yi-Ming MU ◽  
Koichi OBA ◽  
Toshihiko YANASE ◽  
Takeshi ITO ◽  
Kenji ASHIDA ◽  
...  

PROTEOMICS ◽  
2006 ◽  
Vol 6 (3) ◽  
pp. 826-835 ◽  
Author(s):  
Hung Wu ◽  
Ching-Liang Pan ◽  
Yun-Chin Yao ◽  
Shau-Shin Chang ◽  
Shun-Lai Li ◽  
...  

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

2018 ◽  
Vol 106 ◽  
pp. 292-302 ◽  
Author(s):  
Arkadiusz Czerwonka ◽  
Katarzyna Kaławaj ◽  
Adrianna Sławińska-Brych ◽  
Marta K. Lemieszek ◽  
Magdalena Bartnik ◽  
...  

Data in Brief ◽  
2020 ◽  
Vol 30 ◽  
pp. 105497
Author(s):  
Quan Dang Nguyen ◽  
Phung Minh Truong ◽  
Thao Nguyen Thanh Vo ◽  
Truc Dao Xuan Chu ◽  
Chuong Hoang Nguyen

2020 ◽  
Vol 840 ◽  
pp. 277-283
Author(s):  
Melanny Ika Sulistyowaty ◽  
Galih Satrio Putra ◽  
Tutuk Budiati ◽  
Katsuyoshi Matsunami

Some benzylidenehydrazides (3a-e) have been synthesized in three reaction steps from anthranilic acid in good yields, about 70% - 99%. The structures of the synthesized compounds were analyzed using spectroscopic methods. The compounds were evaluated its activity against human lung cancer, A549 cell line by MTT method and studied its molecular docking onto the protein tyrosine kinase (PDB ID: 1M17) by using Molegro® vs. 5.5. The data showed that N-(2-(2-(4-nitrobenzylidene)hydrazinecarbonyl)phenyl)benzamide (3d) which synthesized in 70% yield and has the highest activity on inhibiting the growth of A549 cell line with IC50 10.9μg/mL, which was linier with our in silico study. Compound 3d has the smallest RS value -94.44 kcal/mol, lower than selected Ligand, Erlotinib.


Pharmacology ◽  
2017 ◽  
Vol 100 (5-6) ◽  
pp. 283-291 ◽  
Author(s):  
Zhicheng Huang ◽  
Changliang Yang ◽  
Shuangyan Sun ◽  
Yingji Nan ◽  
Zhiguo Lang ◽  
...  

Lung cancer is one of the major causes of cancer morbidity and mortality around the world, and the resistance to cisplatin is a critical issue to chemotherapy in lung cancer patients. Transforming growth factor β (TGF-β) signal pathway abnormality is widely observed in drug resistance during lung cancer chemotherapy. Here, we investigated the effects of heat-shock protein 27 (HSP27) in the TGF-β-induced cisplatin resistance in lung cancer cell. In this study, our results indicated that the mRNA and protein expression of HSP27 were significantly increased in human lung cancer tissues. TGF-β induced the mRNA and protein expression of HSP27 in human lung cancer cell (A549). Treatment of TGF-β-induced cisplatin resistance in A549 cell through blocking the cisplatin-induced apoptosis and cell death, which characterized as the increasing of cell viability and decreasing of PARP and caspase3 cleavage in the cisplatin-treated cell. Knockdown of SMAD3 attenuated the TGF-β-induced HSP27 expression and restored the TGF-β-induced cisplatin resistance in A549 cell. Additionally, the knockdown of HSP27 blocked TGF-β-induced cisplatin resistance via decreasing cell viability and increasing cell apoptosis in A549 cell. These data therefore suggested that HSP27 is critical to lung cancer progression and TGF-β-induced cisplatin resistance in human lung cancer cell, and may provide an effective clinical strategy in lung cancer patients with resistance to chemotherapy.


2013 ◽  
Vol 91 (4) ◽  
pp. 244-251 ◽  
Author(s):  
Feng-xia Wang ◽  
Ning Wu ◽  
Jian-teng Wei ◽  
Jia Liu ◽  
Jin Zhao ◽  
...  

Eupolyphaga sinensis Walker is an important insect used in Chinese traditional medicine. In this study, we purified a 72-kDa anticancer protein, designated as EPS72, from this species using ammonium sulfate precipitation, ultrafiltration, CM Sepharose Fast Flow cation exchange, Q Sepharose High Performance (HP) anion exchange, Butyl Sepharose HP hydrophobic chromatography, and Superdex 75 gel filtration chromatographic techniques. EPS72 exhibited a potent anticancer activity against the human lung cancer A549 cell line (IC50, 18.76 μg/mL). Further study showed that EPS72 could induce A549 cell detachment and apoptosis, inhibit cell adhesion to fibronectin and collagen IV, and restrain cell migration and invasion. Moreover, EPS72 significantly decreased the expression of β1-integrin. This study suggests that EPS72 could potentially be developed as a novel anticancer therapeutic agent due to its possible antimetastatic activity.


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