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多灶性甲状腺乳头状癌中CD44v6和Survivin的表达及其意义

Significance and expression of CD44v56 and Survivin in multifocal papillary thyroid carcinoma
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摘要 目的探讨多灶性甲状腺乳头状癌(PTC)中CD44v6和Survivin的表达及意义。方法应用免疫组织化学SP法检测47例多灶性PTC中CD44v6和Survivin的表达,并与其癌旁组织及同期122例单灶PTC对照,比较不同临床因素中CD44v6、Survivin表达差异,及CD44v6、Survivin两者在多灶PTC中表达的相关性。结果多灶性PTC占同期PTC的27.8%(47/169),与家族史、淋巴结转移、腺外浸润有关(X^2=4.189,X^2=6.159,X^2=4.079,均P〈0.05),而与性别、年龄、是否是微小癌及癌灶大小无关(均P〉0.05)。多灶性PTC中CD44v6和Survivin阳性表达率为70.2%(33/47)和66.0%(31/47),癌旁组织均为2.1%(1/47),差异均有统计学意义(X^2=47.184,P=0.000;x^2=42.641,P=0.000);CD44v6和Survivin的表达与有无腺外浸润(x^2=4.723,P=0.030;X^2=4.023,P=0.045)、有无淋巴结转移(X^2=5.771,P=0.016;x^2=5.686,P=0.017)有关,而与性别、年龄、家族史、是否是微小癌、病灶数目无关(均P〉0.05);多灶PTC中癌灶间CD44v6和Survivin的表达差异无统计学意义(均P〉0.05);CD44v6和Survivin在多灶PTC中的表达呈正相关(x^2=10.154,P〈0.01)。术后随访5年。9年9个月,两组PTC患者均健在。结论多发癌灶是PTC的临床特征之一,CD44v6和Survivin在多灶性PTC中高表达,与多灶PTC的发生、侵袭和转移密切相关。 Objective To study the relationship between clinical-biological significance and the expression of CD44v6 and Survivin in multifocal papillary thyroid carcinoma (PTC). Methods Immunohistochemical SP method was used to investigate the expression of CD44v6 and Survivin in 47 cases of multifocal PTC and adjacent tissues, and 122 cases of single focal PTC tissues. The expression of CD44v6 and Survivin and the risk factors among different clinical factors were analyzed between solitary PTC and multifocal PTC group. Results Tumor loci were found in 27.8 % (47/169) patients. The patients with muhifocal were characterized by a higher ratio of family history of thymid tumor, lymph node metastasis and extra-thymida] extension (X2 = 4.189, 6.159, 4.079, P 〈0.05), and not related with sex, age, size and the number of the tumors (P 〉0.05). The positive rates of CD44v6 and Survivin were 70.2 % (33/47) and 66.0 % (31/47), respectively, in multifocal PTC, both of which were significantly higher than that in nodular goiter, Hashimoto's thyroiditis and normal thyroid tissues (X2 =47.184, P 〈0.05). Overexpressions of CD44v6 and Survivin in muhifocal PTC were related to the degree of the infiltration(x2 = 4.723, P =0.030; X2 =4.023, P =0.045) and lymph node metastasis (X2 =5.771, P =0.016; )(2 =5.686, P =0.017), and not related with sex, age, family history and the number of the tumors (P 〉0.05). The expression of CD44v6 was correlated positively with Survivin (r =0.514, R2 =10.15, P 〈0.01). There was no significant difference in expressions of CD44v6 and Survivin between muhifocal and single focal PTC (P 〉0.05). By the sept. 2010, the patients with single and mutiple focal PTC were all survival. Conclusion Multifocus is one of the clinical features of PTC. The high expressions of CD44v6 and Survivin in muhifocal PTCs relate to the development, invasion and metastasis.
出处 《肿瘤研究与临床》 CAS 2011年第8期541-544,共4页 Cancer Research and Clinic
关键词 甲状腺肿瘤 乳头状 CD44V6 SURVIVIN Thyroid neoplasms Carcinoma, papillary CD44v6 Survivin
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参考文献12

  • 1Delellis RA,Lioyd RV,Heitz PU,et al.Pathology and genetics of tumors of the endocrine organs.3rd ed.Lyon:IARC Press,2004.
  • 2嵇庆海,王玉龙,郭智.甲状腺癌诊治进展[J].肿瘤研究与临床,2006,18(3):214-216. 被引量:27
  • 3Santoro M,Melillo RM,Fusco A.RET/PTC activation in papillary thyroid carcinoma:European Journal of Endocorinology Prize Lecture.EurJ Endocrinol,2006,155:645-653.
  • 4Shattuck TM,Westra WH,Ladenson PW,et al.Independent clonal origins of distinct tumor foci in multifocal papillary thyroid carcinoma.N EngJ Med,2005,352:2406-2412.
  • 5任晋军,米玉录,孙瑞芳.环氧合酶-2、血管内皮生长因子及上皮钙黏素在甲状腺癌中的表达及其临床意义[J].肿瘤研究与临床,2010,22(6):400-403. 被引量:4
  • 6Sonobe S,Miyamoto H,Nobukawa B,et al.Prognostic value of CD44 isoform expression in thymic epithelial neoplasms.Cancer,2005,103:2015-2022.
  • 7卢秀波,安兆峰,王庆兆,殷德涛,邱新光.Survivin和c-myc在分化型甲状腺癌中的表达及临床意义[J].中华实验外科杂志,2004,21(6):705-706. 被引量:18
  • 8林益凯(综述),赵文和(审校).甲状腺乳头状癌多发病灶的克隆起源研究进展[J].国际肿瘤学杂志,2007,34(9):668-670. 被引量:5
  • 9Chuang CK,Liao SK.Differential expression of CD44 variant isoforms by cell lines and tissue specimens of transitional cell carcinomas.Anticancer Res,2003,23:4635-4639.
  • 10Hoshimoto K,Yamauchi N,Takazawa Y,et al.CD44 variant 6 in endometrioid carcinoma of the uterus:its expression in the adenocarcinoma component is an independent prognostic marker.Pathol Res Pract,2003,199:71-77.

二级参考文献38

  • 1张东伟,杨维良.甲状腺癌基因治疗的现状及展望[J].中华实验外科杂志,2005,22(2):255-256. 被引量:16
  • 2卢秀波,王利,王家祥,娄卫华,余捷凯,郑树.血清蛋白质指纹图谱在甲状腺癌诊断中的应用[J].中华实验外科杂志,2006,23(6):703-705. 被引量:16
  • 3胡礼炳,王国民,张利能,查锡良.膀胱癌细胞中DAPK基因启动子甲基化状态分析[J].中华实验外科杂志,2007,24(4):489-491. 被引量:13
  • 4Feinstein E,Druck T,gastury K,et al.Assignment of DAP1 and DAPK-Genes that positively mediate programmed cell death triggered by IFN-γ-to chromosome regions 5p12.2 and 9q34.1,respectively.Genomics,1995,29:305-307.
  • 5Jin YJ,Blue EK,Gallagher PJ.Control ofdeath-associated protein kinsse(DAPK)activity by phosphorylation and proteasomal degradation.J BiolChem,2006,281:39033-39040.
  • 6Shang T,Joseph J,Hillard CJ,et al.Death-associated protein kinese as a sensor of mitochondrial membrane potentia:l role of lysosome inmitochondrial toxin-induced cell death.J BiolChem,2005,280:34644-34653.
  • 7Kogel D,Reimertz C,Dubm H,et al.The death associated protein(DAP)kinase homologue D1 k/ZIP kinase induces p19ARF and p53-independent apoptosis.Eur J Cancer,2003,39:249-256.
  • 8Hu S,Liu D,Tufano RP,et al.Association of aberrant methylation of tumor suppressorgenes with tumnor aggressiveness and BRAF mutation in papillary thyroid cancer.Int J Cancer,2006,119:2322-2329.
  • 9Yamanaka M,Watanabe M,Yamada Y,et al.Altered mathylation of multiple genes in carcino-genesis of the prostate.Int J CAtncer,2003,106:382-387.
  • 10Bialik S,KimehiA.DAP-kinase as a target fordrug design in cancerand diseases associated with accelerated cell death.Semin Cancer Biol,2004,14:283-294.

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