Liu Jing,Tang Yiting,Zhou Jundong,Zhang Shuyu,Cao Han,Wu Jinchang,Luo Judong,Chen Guanglie,Cao Jianping*.Inhibition effect of proteasome inhibitor MG132 combined with X-ray irradiation on cell growth, metastasis and cycle distribution of human lung adenocarcinoma cells[J].Chinese Journal of Radiological Medicine and Protection,2014,34(1):8-12
Inhibition effect of proteasome inhibitor MG132 combined with X-ray irradiation on cell growth, metastasis and cycle distribution of human lung adenocarcinoma cells
Received:April 26, 2013  
DOI:10.3760/cma.j.issn.0254-5098.2014.01.003
KeyWords:Proteasome inhibitor  MG132  Lung adenocarcinoma  Cell growth  Metastasis  Cell cycle arrest
FundProject:国家自然科学基金(81372433,81172597,81102078);江苏省高校重大科研项目(11KJA310001)
Author NameAffiliationE-mail
Liu Jing School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou 215123, China  
Tang Yiting School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou 215123, China  
Zhou Jundong 南京医科大学附属苏州医院放疗科  
Zhang Shuyu School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou 215123, China  
Cao Han School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou 215123, China  
Wu Jinchang 南京医科大学附属苏州医院放疗科  
Luo Judong School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou 215123, China  
Chen Guanglie School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou 215123, China  
Cao Jianping* School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou 215123, China jpcao@suda.edu.cn 
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Abstract::
      Objective To study the effects of proteasome inhibitor MG132 on the growth, metastasis, and cell cycle distribution of human lung adenocarcinoma cells A549 irradiated by X-rays. Methods After treatment of MG132 and irradiation, cell proliferation was detected by MTT assay. Survival was measured by clonogenic assay. Cell migration ability was detected by the Scratch migration assay. Cell invasion ability was detected by transwell migration assay. Cell cycle distribution were analyzed by flow cytometry assay. Protein expression was detected by Western blot assay. Results MG132 alone inhibited cell growth in a dose-and time-dependent manner. MG132 in combination with radiation significantly suppressed the growth, migration and invasion of A549 cells compared to the control(F=554.78, 954.64,P<0.01). MG132 enhanced radiation-induced G1-arrest(t=4.44, 12.41, 3.52, 6.72, P<0.05). The G1 cell cycle distribution rate of MG132 plus RT group was increased to (71.05±4.17)%. The expressions of MMP-2, MMP-9 and Cyclin D1 were significantly suppressed by MG132 in combination with radiation, while the expression of P53 was up-regulated. Conclusions MG132 inhibits cell growth, migration and invasion ability, and induces G1 cell cycle arrest of A549 cells treated with MG132 in combination with radiation, in which the down-regulation of MMPs and Cyclin D1 and up-regulation of P53 may be involved.
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