期刊文献+

白血病中PTEN mRNA的表达状态研究

Detection of PTEN mRNA expression in leukemia
下载PDF
导出
摘要 目的利用实时PCR技术检测急性粒细胞白血病(AML)、急性淋巴细胞白血病(ALL)和慢性淋巴细胞白血病(CLL)中的PTEN mRNA的表达状况。方法收集病例AML21例,ALL3例和CLL23例,按照相应的情况进行分组,比较各组PTEN mRNA在不同情况下的表达状态。结果 AML和ALL组的目的基因Ct值没有明显差异(P>0.05),且这两组的Ct值要明显高于CLL组的Ct值(P<0.05),这三个组的Ct值要明显高于对照组的Ct值(P<0.05)。AML组和ALL组的初治组Ct值要高于缓解组的Ct值,CLL组的初治组的Ct值和缓解组的Ct值没有明显差异(P>0.05)。AML、ALL和CLL组的高肿瘤负荷组的Ct值要明显高于低肿瘤负荷组的Ct值(P<0.05)。结论通过实验确定了三种病例的PTEN基因表达状况,为疾病的预判和转归可能提供了辅助的可靠地途径。 Objective The aim of the present study was to detect the expression of PTEN mRNA in AML,ALL and CLL using real time PCR. Methods Case AML(21),ALL(3)and CLL(23)are grouped according to the respective situation. The PTEN mRNA expression status in different situations were compared to find out the difference. Results The gene of AML and ALL Ct values did not differ significantly( P﹥0. 05). These Ct value of two groups was significantly higher than the Ct value of CLL group( P ﹤0. 05). The three groups Ct values were significantly higher than the Ct values( P ﹤0. 05). The Ct values of untreated AML and ALL groups were higher than the Ct values remission group. Meanwhile no significant difference was found in untreated and remittent group of CLL( P ﹥0. 05). The Ct value of the high tumor burden group in AML,ALL and CLL was significantly higher than that of the Ct value of low tumor burden group( P ﹤0. 05). Conclusion Our study indicated that detection of PTEN gene expression may provide a reliable way to predict the outcome of the disease.
作者 丁志勇
出处 《临床和实验医学杂志》 2014年第23期1957-1959,共3页 Journal of Clinical and Experimental Medicine
关键词 CLL AML ALL PTEN 实时PCR 脆性基因 CLL AML ALL PTEN Real fine PCR Brittle gene
  • 相关文献

参考文献10

  • 1PaIamarchuk A,Yan PS,Zanesi N,et ah Tcll protein functions as an inhibitor of de novo DNA methylation in B-cell chronic lymphocytic leukemia(CLL)[J].Proc Natl Acad Sci USA,2012,109(7):2555-2560.
  • 2Takeuchi S,Matsushita M,Zimmermann M,et al.Clinical significance of aberrant DNA methylation in childhood acute lymphoblastic leukemia [J].Leuk Res,2011,35(10):1345-1349.
  • 3沈丽佳,谢思明,殷操,阮萍,姚希.抑癌基因PTEN和FHIT在口腔鳞癌中的表达及其与cyclin D1的相关性[J].第一军医大学学报,2005,25(1):79-82. 被引量:14
  • 4Chen X,Zhang H,Li P,et al.Gene expression of WWOX,FHIT and p73 in acute lymphoblastic leukemia[J].Oncol Lett,2013,6(4):963-969.
  • 5Stam RW,den Boer ML,Passier MM,et al.Silencing of the tumor suppressor gene FHIT is highly characteristic for MLL gene rearranged infant acute lymph leukemia[J].Leukemia,2006,20(2):264-271.
  • 6Bednarek AK,Keck Waggoner CL,Daniel RL,et al.WWOX,the FRA16D gene,behaves as a suppressor of tumor growth [J].Cancer Res,2001,61(22):8068-8073.
  • 7Guler G,Huebner K,Himmetoglu C,et al.Fragile histidine triad pro- tein,WW domain - containing oxidoreductase protein WWOX,and acti- vator protein2 gamma expression levels correlate with basal Phenotype in breast cancer[J].Cancer,2009,115(4):899-908.
  • 8Lewandowska U,Zelazowski M,Sela K,et al.WWOX,the tumour suppressor gene affected in multiple cancers [J].J Physiol Pharmacol,2009,60(6):47-56.
  • 9Ishii H,Vecchione A,Fumkawa Y,et al.Expression of FRA16D/ WWOX and FRA3 B/FHIT genes in hematopoietic malignancies [J].Mol Cancer Res,2003,1(13):940-947.
  • 10周民,岑岭,蒋红.儿童与成人急性淋巴细胞白血病的临床及细胞遗传学比较分析[J].临床荟萃,2007,22(22):1627-1628. 被引量:4

二级参考文献10

  • 1Steck PA, Pershouse MA, Jasser SA, et al. Identification of a candidate tumour suppressor gene, MMAC 1, at chromosome 10q23.3 that is mutated in multiple advanced cancers[J]. Nat Genet, 1997, 15(4):356-62.
  • 2Van Heerden W F, Swart T J, Robson B, et al. FHIT RNA and protein expression in oral squamous cell carcinomas [J]. Anticancer Res, 2001, 21 (4A): 2425-8.
  • 3Chen Q, L.P. Samaranayake LP, Zhou H, et al. Homozygous deletion of the PTEN tumor-suppressor gene is not a feature in oral squamous cell carcinoma[J]. Oral Oncol, 2000, 36(1): 95-9.
  • 4van Heerden WF, Swart T J, Robson B, et al. FHIT RNA and protein expression in oral squamous cell carcinomas [J]. Anticancer Res,2001, 21 (4A): 2425-8.
  • 5Ohta M, Inoue H, Cotticelli M G, et al. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma associated t (3;8) breakpoint, is abnormal in digestive tract cancers [ J ]. Cell, 1996,84(4): 587-97.
  • 6Lee JI, Soria J C, Hassan K. Loss of ghit rxpression is a predictor of poor outcome in tongue cancer [ J ]. Cancer Research, 2001, 61: 837-41.
  • 7Furnari FB, Huang HJ, Cavenee WK. The phosphoinositol phosphatase activity of PTEN mediates a serum-sensitive G1 growth arrest in glioma cells[J]. Cancer Res, 1998, 58(22): 5002-8.
  • 8Barne S, Larry D, Garriso N, et al. Fhit, a putative tumor suppressor in humans, is a dinucleoside 5′, 5"-P1, P3-triphosphate hydrolase [J ].Biochemistry, 1996, 35(36): 11529-35.
  • 9Subol RB,Mick R,Royston I,et al.Clinical importance myeloid antigen expression in adult lymphocytic leukemia[J].N Engl J Med,1997,316(18):1111-1117.
  • 10周传香,高文信,魏秀峰.口腔鳞癌发展过程中抑癌基因PTEN的蛋白表达及意义[J].口腔医学研究,2003,19(5):365-367. 被引量:6

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