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姜黄素诱导人成骨肉瘤MG-63细胞凋亡过程中核基质蛋白表达的变化 被引量:2

CHANGES OF NUCLEAR MATRIX PROTEINS DURING APOPTOSIS OF HUMAN OSTEOSARCOMA MG-63 CELLS INDUCED BY CURCUMIN
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摘要 应用选择性抽提、整装透射电镜观察和双向聚丙烯酰胺凝胶电泳与质谱鉴定技术研究细胞凋亡诱导物姜黄素处理前后人成骨肉瘤MG-63细胞核基质-中间纤维系统的构型变化.及其核基质蛋白表达的差异。经姜黄素处理后.MG-63细胞的核基质和中间纤维比对照组明显稀疏,且分布更加不均匀,并分别与核纤层连系,形成趋于断裂但相对还较为完整的网状结构:双向凝胶电泳分析显示在姜黄素诱导MG-63细胞凋亡前后存在27个差异表达的核基质蛋白,经质谱鉴定了其中的21个蛋白.在凋亡的MG-63细胞中表达上调的蛋白鉴定为:DNA聚合酶zeta等7种蛋白:表达下调的蛋白质为:Prohibitin等14种蛋白。其中首次在核基质中发现的蛋白质有17个。因此,在MG-63细胞凋亡过程中不仅其核基质-中间纤维系统构型产生了典型的的凋亡特征性变化.而且伴有核基质蛋白表达的差异。由此证实了与肿瘤细胞凋亡诱导相关特异核基质蛋白的存在及其对肿瘤细胞凋亡诱导的调控作用.从而对揭示核基质构型及其蛋白组成与细胞凋亡的关系和阐明细胞凋亡过程中的基因表达调控机理.均具有重要意义。 Human osteosarcoma MG-63 cells were induced into apoptosis by curcumin (Cur) . Its nuclear matrix proteins were selectively extracted, and subjected to two dimensional gel electrophoresis analysis. The resulted protein patterns were analyzed by Melanie software. There were 27 spots changed remarkably during the apoptosis induced by curcumin, 21 of which were identified. There were seven up-regulated proteins including DNA polymerase zeta and forteen down-regulated proteins including Prohibitin. This study suggests that the induced apoptosis of carcinoma cells is accompanied with changes of nuclear matrix proteins, and confirms the presence of some specific nuclear matrix proteins associated with carcinoma cell growth, apoptosis and the associated signal transduction pathways in induced apoptosis of carcinoma cells. It provides proofs and a new way to study the mechanisms of gene expression carcinogenesis which reveal the relationship between configuration and composition of nuclear matrix and cell apoptosis. Besides, this study provides several potential target proteins for cancer diagnosis and cancer therapy.
出处 《分子细胞生物学报》 CSCD 北大核心 2008年第6期473-481,共9页 Journal of Molecular Cell Biology
基金 国家自然科学基金项目(30470877)~~
关键词 人成骨肉瘤细胞 细胞凋亡 姜黄素 核基质-中间纤维系统 核基质蛋白 Human osteosarcoma. Apoptosis. Curcumin. Nuclear matrix-intermediate filament. Nuclear matrix protein
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  • 1Tsutsui KM, Sano K & Tsutsui K, Dynamic view of the nuclear matrix. Acta Med Okayama, 2005, 59(4) : 113-120.
  • 2Radichev I, Parashkevova A & Annchkova B, Initiation of fraction. Journal of cellular physiology, 2005, 203: 71-77.
  • 3Larovaia OV, Akopov SB, Nikolaev LG, Sverdlov ED & Razin SV, Induction of transcription within chromosomal DNA loops flanked by MAR elements causes an association of loop DNA with the nuclear matrix. Nucleic Acids Research, 2005, 33(13): 4157-4163.
  • 4Otake Y, Mims A & Femandes D J, Merbarone induces activation of caspase-activated DNase and eccision chromosomal DNA loops from the nuclear matrix. Mol Pharmacol. 2006, 69(4) : 1 477-1 485.
  • 5李念,邵淑丽.姜黄素诱导肿瘤细胞凋亡机制的研究进展[J].高师理科学刊,2007,27(1):27-30. 被引量:13
  • 6Peng XX, Ye XT & Wang SY, Identification of novel immunogenic proteins of shigella flexneri 2a by proteomic methodologies. Vaccine, 2004, 22:2 750-2 756.
  • 7Bosman FT, The nuclear matrix in pathology. Virchows Arch, 1999, 435 (4): 391- 399.
  • 8Zhang QX, Ding Y, Li Z, Le XP , Zhang W, Sun L & Shi HR. Comparison of nuclear matrix proteins between gastric cancer and normal gastric tissue. World J Gastroenterol, 2004, 10(12) : 1 819- 1 821.
  • 9Mgbonyebi OP, Russo J & Russo IH. Roscovitine induces cell death and morphological changes indicative of apoptosis in MDA-MB-231 breast cancer cells. Cancer Research. 1999, 59: 1 903-1 910.
  • 10Flusberg DA, Numaguchi Y & Ingber DE. Cooperative control of Akt phosphorylation, bcl-2 expression, and apoptosis by cytoskeletal microfilaments and microtubules in capillary endothelial cells. Molecular Biology of the Cell, 2001 , 12:3 087-3 094.

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  • 1王振义,孙关林,陈竺.诱导分化疗法应用的现状[J].中华血液学杂志,1994,15(2):105-107. 被引量:28
  • 2杨彤涛,牛子长,李存孝,黄立军,高杰,马保安,范清宇,周勇.表没食子儿茶素-3-没食子酸酯抑制骨肉瘤细胞增殖及其机制[J].实用医学杂志,2007,23(10):1449-1451. 被引量:7
  • 3陶海,蔡林.多西紫杉醇联合顺铂在人骨肉瘤化疗中的作用[J].中国矫形外科杂志,2007,15(11):856-859. 被引量:2
  • 4Nishikawa M, Otsuki T, Ota A, et al. Induction of tumor-specific immune response by gene transfer of Hsp70-cell-penetrating peptide fusion protein to tumors in mice [J]. Mol Ther, 2010, 18 (2) : 421 428.
  • 5Kotoglou P, Kalaitzakis A, Vezyraki P, et al. HspT0 translocates to the nuclei and nucleoli, binds to XRCC1 and PARP-1, and protects HeLa cells from single-strand DNA breaks [J]. Cell Stress Chaperones, 2009, 14(4) : 391-406.
  • 6Chen Y, Zhao M, Wang S, et al. A novel role for DYXICI, a chaperone protein for both Hsp70 and Hsp90, in breast cancer[J]. J Cancer Res Clin Oncol, 2009, 135(9) : 1265-1276.
  • 7Maehara Y, Oki E, Abe T, et al. Overexpression of the heat shock protein HSP70 family and p53 protein and prognosis for patients with gastric cancer[J]. Oncology, 2000, 58 (2) : 144-151.
  • 8Li H, Sui C, Kong F, et al. Expression of HSPT0 clinical outcome proteins in human liver cancer: Potential effects on and JNK-related [J]. Dig Liver Dis, 2007, 39 (7) : 663-670.
  • 9Kumar S, Deepak P, Acharya A. Hsp70 induces Thl polarization through tumor-associated macrophages in a T-cell lymphoma [J]. Neoplasma, 2007, 54(2) : 113-122.
  • 10Tanimura S, Hirano AI, Hashizume J, et al. Anticancer drugs up- regulate HspBP1 and thereby antagonize the prosurvival function of Hsp70 in tumorcells[J]. J Biol Chem, 2007, 282(49): 35430- 35439.

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