期刊文献+

微卫星杂合性缺失与甲状腺癌相关性研究

Study on the correlation between the loss of microsatellite heterozygosity and thyroid carcinoma
下载PDF
导出
摘要 目的探讨特定位点微卫星杂合性缺失(LOH)与人甲状腺癌发生、临床病理特征及预后的关系。方法选取THRA1,D2S123,D11S912,BAT-264个位点,应用聚合酶链反应(PCR)和变性聚丙烯酰胺凝胶电泳技术,对30例甲状腺癌中LOH表达情况进行研究,术后随访5年,了解预后。结果THRA1,D2S123,D11S912,BAT-26四个位点LOH的检出率分别为33.3%,26.7%,23.3%和16.7%。术后随访5年,LOH阳性的甲状腺癌较阴性者生存期更长(P<0.05)。结论LOH导致基因组不稳定,在甲状腺肿瘤发生过程中发挥作用。 Objective To investigate the correlation between the loss of microsatellite heterozygosity (LOH) and thyroid carcinoma, and to explore the relationship between the clinical pathological features of thyroid carcinoma and patients' prognoses. Methods The 4 sites including THRA1, D2S123, D11S912, BAT-26 were selected,and polymerase chain reaction (PCR) and denaturing polyacrylamide gel electrophoretic technique were used to detect the expression of LOH in 30 patients with thyroid carcinoma. The patients ' prognoses were evaluated by 5-year follow-up. Results The detection rates of LOH at the 4 sites including THRA1, D2S123, D11 $912, BAT-26 were 33.3% (20/60) ,26.7% (16/60) ,23.3% (14/60) and 16.7% (10/60) respectively. After 5-year follow-up, the survival time in patients with positive LOH was much longer than that of patients with negative LOH( P 〈 0.05). Conclusion LOH leads to the instability of the genome, which may result in the genesis of thyroid caicinoma. The patients with positive LOH have longer survival time.
出处 《河北医药》 CAS 2009年第17期2210-2212,共3页 Hebei Medical Journal
基金 河北省科学技术研究与发展攻关计划项目资助课题(编号:062761203)
关键词 甲状腺肿瘤 微卫星杂合性缺失 聚合酶链反应 thyroid carcinoma LOH PCR
  • 相关文献

参考文献13

  • 1Hundahl S,Cady B,Cunningham MP,et al.Initial results from a prospective cohort study of 5583 cases of thyroid carcinoma treated in the united states during 1996.Cancer (Phila),2000,89:202-217.
  • 2Goretzki PE,Witte J,Dotzenrath C,et al.Geographical differences of thyroid carcinoma and basic molecular principles.Langenbecks Arch Chir Suppl Kongressbd,1998,115:200-202.
  • 3Esteller M,Levine R,Baylin SB,et al.MLH1 promoter hypermethylation is associated with the microsatellite instability phenotype in sporadic endometrial carcinomas.PMID,1998,17:2413-2417.
  • 4翟瑜,苏力,杜权,杨月卿,郭贵军,李保庆,单保恩,王桂琦.食管癌组织3p、18q位点微卫星DNA序列不稳定性的研究[J].诊断学理论与实践,2005,4(2):145-149. 被引量:8
  • 5Catasus L,Machin P,Matias-Guiu X,et al.Microsatellite instability in endometrial carcinomas:clinicopatholoigic correlations in a series of 42 cases.Hum Pathol,1998,29:1160-1164.
  • 6翟瑜,苏力,王桂琦,李保庆,单保恩.微卫星不稳定性与食管癌的关系[J].中华胸心血管外科杂志,2003,19(3):187-189. 被引量:7
  • 7Ionov Y,Peinado MA,Malkhoayans B,et al.Ubiquitous somatic mutation in simple repeated sequences reveal a new mechanism for colonic carcinogenesis.Nature,1993,363:558-561.
  • 8Helland A,Borresen-Dale AL,Peltomaki P,et al.Microsatellite instability in cervical and endometrial carcinomas.Int J Cancer,1997,70:499-501.
  • 9Vaish M,Mishra SK,Mandhani A,et al.Assessment of microsatellite instability in bladder and thyroid malignancies.Teratog Carcinog Mutagen,2003,suppl:255-265.
  • 10Vaish M,Mishra A,Kaushal M,et al.Microsatellite instability and its correlation with clinicopathological features in a series of thyroid tumors prevalent in iodine deficient areas.Exp Mol Med,2004,36:122-129.

二级参考文献41

  • 1李卫东,王亮,王秀琴,张春林,张涛,毛学正,吴旻.食管癌组织染色体位点特异性的杂合性丢失和微卫星DNA序列不稳定[J].中华医学遗传学杂志,1996,13(4):194-197. 被引量:17
  • 2[3]Catasus L, Machin P, Matias-Guiu X, et al. Microsatellite instability in endometrial carcinomas: clinicopatholoigic correlations in a series of 42 cases[J]. Hum Pathol, 1998,29(10):1160-1164.
  • 3[4]Ionov Y, Peinado MA, Malkhosyan S, et al. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis [J]. Nature,1993,363(6429):558-561.
  • 4[5]Helland A, Borresen-Dale AL, Peltomaki P, et al. Microsatellite instability in cervical and endometrial carcinomas[J]. Int J Cancer, 1997,70(5):499-501.
  • 5[6]Meltzer SJ, Yin J, Manin B, et al. Microsatellite instability occurs frequently and in both diploid and aneuploid cell populations of Barrett's-associated esophageal adenocarcinomas [J]. Cancer Res, 1994, 54(13):3379-3382.
  • 6[7]Kulke MH, Thakore KS, Thomas G, et al. Microsatellite instability and hMLH1/hMSH2 expression in Barrett esophagus- associated adenocarcinoma[J]. Cancer, 2001,91(8):1451-1457.
  • 7[8]Nakashima H, Mori M, Mimori K. Microsatellite instability in Japanese esophageal carcinoma [J]. Int J Cancer,1995,64(4):286-289.
  • 8[9]Ogasawara S, Maesawa C, Tamura G. Frequent microsatellite alterations on chromosome 3p in esophageal squamous cell carcinoma[J]. Cancer Res, 1995,55(4):891-894
  • 9[12]Mathew R, Arora S, Mathur M, et al. Esophageal squamous cell carcinomas with DNA replication errors (RER+)are associated with p16/pRb loss and wild-type p53[J]. J Cancer Res Clin Oncol, 2001,127(10):603-612.
  • 10[13]Sanchez-Cespedes M, Monzo M, Rosell R, et al. Detection of chromosome 3p alterations in serum DNA of nonsmall-cell lung cancer patients[J]. Ann Oncol, 1998,9(1):113-116.

共引文献11

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