期刊文献+

Bub1和Mad2蛋白在子宫内膜癌中的表达及意义

Expression and Clinical Significance of Bub1 and Mad2 Protein in Endometrial Carcinoma
下载PDF
导出
摘要 目的探讨苯并咪唑出芽抑制解除同源物蛋白-1(Bub1)和有丝分裂阻滞缺陷蛋白-2(Mad2)在人子宫内膜癌中的表达情况。方法采用免疫组织化学SP法分别检测72例子宫内膜癌组织(A组)、40例子宫内膜不典型增生组织(B组)和40例人正常子宫内膜组织(C组)中Bub1和Mad2蛋白的表达情况,并分析其与子宫内膜癌患者的临床分期、病理分级和淋巴结转移的关系。结果 (1)Bub1蛋白在A,B,C组的阳性表达率分别为27.78%,57.50%,85.00%,3组间比较差别有统计学意义(P<0.05);A组中,不同临床分期或病理分级患者的Bub1蛋白阳性表达率差别有统计学意义(P<0.05),有、无淋巴结转移患者的阳性表达率差别无统计学意义(P>0.05)。(2)Mad2蛋白在A,B,C组的阳性表达率分别为86.11%,57.50%,22.50%,3组间比较差别有统计学意义(P<0.05);A组中,不同病理分级患者的Mad2蛋白阳性表达率差别有统计学意义(P<0.05),不同临床分期及有、无淋巴结转移患者的Mad2蛋白阳性表达率差别无统计学意义(P>0.05)。(3)Bub1和Mad2蛋白在子宫内膜癌组织中的表达呈负相关(r=-0.448,P<0.01)。结论 Bub1和Mad2蛋白相互作用,在子宫内膜癌的发生、发展过程中可能起重要作用。 Objective To investigate the expression and clinical significance of budding uninhibit ed by benzimidazoles-1(gub1) and mitotic arrest deficient-2 (Mad2) protein in endometrium, complex hyperplasia and endometrial carcinoma. Methods The expression of Bubl and Mad2 protein in 72 cases of endometriat carcinoma(group A), 40 cases of complex endometrial hyperplasia(group B) and 40 cases of endometrial(group C) were detected by Immunohistochemistal SP method, and the relationship between the expression of Bubl, Mad2 protein and the clinical stage, pathological classification and lymph node metastasis of endometrial carcinoma patients was analysed. Results (1) The positive rate of Bubl in A, B, C groups were 27.78%, 57.50%, 85.00% respectively, positive expression rate between the three groups was statistically significant (P〈0. 05). In group A, different clinical stage or pathologic stage in patients,the positive expression rate was statistically significant difference (P〈0.05). In group A,with or without lymph node metastasis in patients, the positive expression rate was no statistically significant difference (P〈0. 05). (2) The positive rate of Mad2 in A, B, C groups were 86. 11%, 57. 50%, 22.50% respectively, positive expression rate between the three groups was statistically significant (P〈0.05). In group A,different pathological grading in patients,the positive expression rate was statis- tically significant difference (P〈0.05). In group A,different clinical stages and with or without lymph node metastases in patients, the positive expression rate there was no statistically significant difference (P〉0.05). (3)The expression of Bubl and Mad2 protein negatively correlated in endometrial carcinoma (r=0. 448, P〈0.01). Conclusion The interaction of Bubl with Mad2 proteins may play an important role in the pathological process of endometrial carcinoma.
出处 《福建医科大学学报》 2013年第2期98-101,共4页 Journal of Fujian Medical University
关键词 子宫内膜肿瘤 蛋白质类 有丝分裂纺锤体 endometrial neoplasms oncogene proteins mitotic spindle apparatus
  • 相关文献

参考文献10

  • 1Ito D, Saito Y, Matsumoto T. Centromere-tethered Mpsl pornbe homolog (Mphl) kinase is a sufficient marker for re cruitment of the spindle checkpoint protein Bubl, but not Madl[J]. Proc Natl Acad Sci USA, 2012,109(1):209-214.
  • 2李志琴,章静波.细胞周期调控与肿瘤(2)[J].癌症进展,2004,2(2):146-150. 被引量:17
  • 3Gao F, Ponte J F, Papageorgis P, et al. hBubl deficiency triggers a novel p53 mediated early apoptotic checkpoint path- way in mitotic spindle damaged cells[J]. Cancer Biol Ther, 2009,8(7):627-635.
  • 4马哲,刘力.子宫内膜癌DNA倍体、SPF的检测及其临床意义的研究[J].中国妇幼保健,2006,21(22):3173-3175. 被引量:1
  • 5Todorovic-Rakovic N. Genome-based versus gene-based theory of cancer: possible implications {or clinical practicc[J]. Bio- sc, 2011,36(4) :719-724.
  • 6Du J, Du Q, Zhang Y, etal. Expression of cell-cycle regulato ry proteins BUBR1, MAD2, Aurora A, cyclin A and eyclin E in invasive ductal breast carcinomas[J]. Histol Histopatho, 2011,26(6) :761-768.
  • 7Kabeehe L, Compton D A. Checkpoint independent stabiliza- tion of kinetochore-microtubule attachments by Mad2 in hu- mancells[J]. CurrBio, 2012,22(7)~638 644.
  • 8Sotillo R, Hernando E, Diaz-Rodriguez E, et al. Mad2 over- expression promotes aneuploidy and tumorigenesis in mice [J]. Cancer Cell, 2007,11 (1) : 9 23.
  • 9Ge S, Skaar J R, Pagano M. APC/C- and Mad2 mediated degradation of Cdc20 during spindle checkpoint activation [J]. Cell Cycle, 2009,8(1):167-171.
  • 10Saitoh S, Kobayashi Y, Ogiyama Y, etal. Dual regulation of Mad2 localization on kinetochores by Bubl and DamI/DASH that ensure proper spindle interaction [J]. Mol Biol Cel, 2008,19(9) :3885-3897.

二级参考文献5

共引文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部