Effects of IKK16 on proliferation and apoptosis of esophageal carcinoma cell line Eca-109
Sha Shi-y
Abstract
Sha Shi-y
Abstract
OBJECTIVE To investigate the effects of IκB kinase inhibitor IKK16 on proliferation and apoptosis of esophageal carcinoma cell line Eca-109.METHODS The human esophageal cancer cell line Eca109 was cultured in vitro and divided into three groups:blank control group(no drug added),low concentration group(70 nmol·L-1)and high concentration group(200nmol·L-1).Methyl thiazolyl tetrazolium(MTT)method was used to detect the proliferation of Eca109 cells with drug added after 24,48 and 72 hours.Western blot was used to investigate the expression of p65,IκB,caspase-3 and Bcl-2 48 hours later.RESULTS Compared to blank control group,IKK16 in groups of two concentrations could significantly suppress the proliferation of Eca-109 cells,inhibit expression of p65 in nucleus(P0.05),and increase IκB in cytoplasm(P0.05).IKK16 could also obviously increase expression of caspase-3(P0.05)and reduce expression of Bcl-2(P0.05)in a dose dependent manner.CONCLUSION IKK16 can inhibit proliferation and promote apoptosis of Eca109 cells,therefore,it may be considered as apotential therapeutic drug against esophageal carcinoma.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
OBJECTIVE To investigate the effects of IκB kinase inhibitor IKK16 on proliferation and apoptosis of esophageal carcinoma cell line Eca-109.METHODS The human esophageal cancer cell line Eca109 was cultured in vitro and divided into three groups:blank control group(no drug added),low concentration group(70 nmol·L-1)and high concentration group(200nmol·L-1).Methyl thiazolyl tetrazolium(MTT)method was used to detect the proliferation of Eca109 cells with drug added after 24,48 and 72 hours.Western blot was used to investigate the expression of p65,IκB,caspase-3 and Bcl-2 48 hours later.RESULTS Compared to blank control group,IKK16 in groups of two concentrations could significantly suppress the proliferation of Eca-109 cells,inhibit expression of p65 in nucleus(P0.05),and increase IκB in cytoplasm(P0.05).IKK16 could also obviously increase expression of caspase-3(P0.05)and reduce expression of Bcl-2(P0.05)in a dose dependent manner.CONCLUSION IKK16 can inhibit proliferation and promote apoptosis of Eca109 cells,therefore,it may be considered as apotential therapeutic drug against esophageal carcinoma.
Key concepts: Apoptosis, Cell growth, Western blot, Cell culture, In vitro, Molecular biology, Carcinoma, Chemistry