中国生物化学与分子生物学报
中國生物化學與分子生物學報
중국생물화학여분자생물학보
CHINESE JOURNAL OF BIOCHEMISTRY AND MOLECULAR BIOLOGY
2008年
1期
11-19
,共9页
贾小芳%石妮%熊继先%谢锦云%梁宋平
賈小芳%石妮%熊繼先%謝錦雲%樑宋平
가소방%석니%웅계선%사금운%량송평
鼻咽癌%细胞系%质谱%双向凝胶电泳%蛋白质组学
鼻嚥癌%細胞繫%質譜%雙嚮凝膠電泳%蛋白質組學
비인암%세포계%질보%쌍향응효전영%단백질조학
nasopharyngeal carcinoma%cell line%mass spectrometry%2 DE%proteomics
鼻咽癌对我国南部居民的健康造成严重的威胁.为了研究鼻咽癌的发病机理,本研究采用了蛋白质组学技术分析和比较了鼻咽癌细胞系(HNE1和CNE1)与永生化的鼻咽上皮细胞系的蛋白质表达谱.采用双向凝胶电泳分离提取的全细胞蛋白质,通过PDQuest软件分析找出在肿瘤中表达变化的蛋白质点,用基质辅助激光解析电离飞行时间串联质谱(MALDI-TOF/TOF-MS)进行鉴定.共得到了15个在肿瘤细胞系中表达上调和18个在肿瘤细胞系中表达下调的蛋白质,并对其中一些蛋白质的表达进行免疫印迹的验证.这些表达差异的蛋白质与细胞的增殖和调亡、癌症的转移,细胞骨架,信号传导等有关.本研究鉴定了一批可能作为鼻咽癌治疗的药物靶标的蛋白质,并对研究鼻咽癌发病机理提供了相关的线索.
鼻嚥癌對我國南部居民的健康造成嚴重的威脅.為瞭研究鼻嚥癌的髮病機理,本研究採用瞭蛋白質組學技術分析和比較瞭鼻嚥癌細胞繫(HNE1和CNE1)與永生化的鼻嚥上皮細胞繫的蛋白質錶達譜.採用雙嚮凝膠電泳分離提取的全細胞蛋白質,通過PDQuest軟件分析找齣在腫瘤中錶達變化的蛋白質點,用基質輔助激光解析電離飛行時間串聯質譜(MALDI-TOF/TOF-MS)進行鑒定.共得到瞭15箇在腫瘤細胞繫中錶達上調和18箇在腫瘤細胞繫中錶達下調的蛋白質,併對其中一些蛋白質的錶達進行免疫印跡的驗證.這些錶達差異的蛋白質與細胞的增殖和調亡、癌癥的轉移,細胞骨架,信號傳導等有關.本研究鑒定瞭一批可能作為鼻嚥癌治療的藥物靶標的蛋白質,併對研究鼻嚥癌髮病機理提供瞭相關的線索.
비인암대아국남부거민적건강조성엄중적위협.위료연구비인암적발병궤리,본연구채용료단백질조학기술분석화비교료비인암세포계(HNE1화CNE1)여영생화적비인상피세포계적단백질표체보.채용쌍향응효전영분리제취적전세포단백질,통과PDQuest연건분석조출재종류중표체변화적단백질점,용기질보조격광해석전리비행시간천련질보(MALDI-TOF/TOF-MS)진행감정.공득도료15개재종류세포계중표체상조화18개재종류세포계중표체하조적단백질,병대기중일사단백질적표체진행면역인적적험증.저사표체차이적단백질여세포적증식화조망、암증적전이,세포골가,신호전도등유관.본연구감정료일비가능작위비인암치료적약물파표적단백질,병대연구비인암발병궤리제공료상관적선색.
Nasopharyngeal carcinoma (NPC) poses serious health problems in Southern China and yet the molecular mechanism of the carcinogenesis remains unclear. We used modern proteomic technologies to compare the protein expression profiles between the NPC cell lines (HNE1 and CNE1 ) and an immortalized nasopharyngeal epithelial cell line NP69 to identify cancer related proteins. Cell lysates were separated by two-dimensional gel electrophoresis (2 DE ) and analyzed by PDQuest software. The differentially expressed proteins were identified by matrix-assisted laser desorption/ionization tandem time-of-flight mass spectrometry (MALDI-TOF/TOF-MS). We discovered 15 up-regulated proteins and 18 down-regulated proteins in both HNE1 and CNE1 cell lines compared with NP69. These proteins are correlative with various functions, such as cell proliferation, apoptosis, cancer metastasis, metabolism, cytoskeleton and signal transduction. Western blotting analyses were further carried out to verify the differential expression of individual proteins. Several identified proteins in our research might be used as potential molecular markers to understand the molecular mechanism of NPC development and metastasis, and might be used as candidate targets for NPC treatments.