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中期因子蛋白表达与子宫内膜腺癌进展的关系 被引量:3

Relationship between midkine protein expression and the progression of endometrial adenocarcinoma
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摘要 目的探讨中期因子(midkineMK)蛋白在子宫内膜腺癌中的表达和进展的关系。方法采用免疫组织化学EnVision法检测72例子宫内膜腺癌组织、15例子宫内膜非典型增生和20例正常子宫内膜组织中MK蛋白的表达情况,并结合患者临床及病理资料进行分析。结果子宫内膜腺癌、子宫内膜非典型增生、正常子宫内膜组织中MK蛋白阳性表达率分别为63.9%、33.3%、15.0%,子宫内膜腺癌中MK蛋白阳性率明显高于子宫内膜非典型增生(P<0.01)和正常子宫内膜(P<0.01)。随着肌层浸润深度、TNM分期的增加,MK蛋白的阳性率显著上升(P<0.01、P<0.05);有淋巴结转移组MK阳性率明显高于无淋巴结转移组(P<0.05);MK蛋白阳性的患者总的生存率低于阴性者(P<0.05)。结论MK蛋白在子宫内膜腺癌恶性进程中表达上调,有望成为子宫内膜腺癌恶性度评估和判断预后的有价值指标。 Objective To investigate the expression of midkine(MK) protein and its correlation with the progression of endometrial adenocarcinoma. Methods Immunohistochemical staining(EnVision)was used to detect the expression of MK protein in 72 cases of endometrial adenocarcinoma, 15 cases of uterine atypical endometrial hyperplasia and 20 cases of normal endometrium. Results The expression rates of MK protein in endometrial adenocareinoma, uterine atypical endometrial hyperplasia and normal endometrium were 63.9%, 33.3% and 15.0% respectively. The positive rate of MK protein in endometrial adenocarcinoma was higher than that in uterine atypical endometrial hyperplasia( P 〈 0.01 )and normal endometrium( P 〈 0.01 ). With the increasing of myometrium invasion depth and TNM grade, the positive rate of MK protein expression increased( P 〈 0.01, P 〈 0.05). The expression rate of MK protein in lymph node metastatic group was higher than those without metastasis( P 〈 0.05). The overall survival rates in patients with MK protein positive were lower than those in patients with MK protein negative( P 〈 0.05). Conclusion The expression rates of MK protein is increased during the malignant progresion in endometrial adenocarcinoma. It might be valuable index to evaluate the degree of malignancy and prognosis of patients in endometrial adenocarcinoma.
出处 《实用肿瘤学杂志》 CAS 2007年第6期519-521,共3页 Practical Oncology Journal
关键词 子宫内膜肿瘤 腺癌 中期因子 转移 预后 Endometrial neoplasms Adenocarcinoma Midkine Metastasis Prognosis
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  • 1金冬雁(译),分子克隆实验指南(第2版),1993年,55页
  • 2Ikenmtsu S, Yano A, Aridome K, et al. Serum midkine levels are increased in patients with various types of carcinomas [ J ]. Br J Cancer ,2000,83 ( 6 ) :701-706.
  • 3Konishi N, Nakamura M, Nakaoka S, et al. Immunohistchemical analysis of midkine expression in human protate carcinoma [ J ].Omcology, 1999,57 ( 3 ) :253-257.
  • 4Kato M , Shinozawa T, Kato S, et al. Increased midkine expression in hepatocellular carcinoma[ J ]. Aech Pathol Lab Med, 2000,124(6) :848-852.
  • 5Muramatsu H, Shirhama H, Yonezawa S,et al. Midkine,a retinoic acidinducible growth/differetiation factor: immunochemical evidence for the function and distribution [ J ]. Dev Biol, 1993 ; 159( 2 ) : 392-402.
  • 6Sakitani H , Tsutsumi M, Kadomatsu K, et al. Overepression of midkine in lung tumors induced by N-nitrosobis (2-hydroxyropy) amine in rats and its increase with progression [ J ]. Carcinogenrsis,1999,20 ( 3 ) :465-469.
  • 7Acenero M J, Gonzalez JF, Gallego MG,et al. Vascular enumeration as a significator for invasive brest carcinoma [ J ]. J Clin Oncol,1998,16 ( 5 ) : 1684-1688.
  • 8Muramatsu H,Song XJ,Koide N,et al.Enzyme-linked immunoassay for midkine,and its application to evaluation of midkine levels in developing mouse brain and sera from patients with hepatocellular carcinomas.J Biochem,1996,119:1171-1175.
  • 9薛泳涛,黄文晋,石斌,陈镔复,鞠躬.MK表达载体的构建及在大肠杆菌中的表达[J].生物化学与生物物理进展,1998,25(1):56-60. 被引量:20
  • 10罗祥基,殷正丰,吴孟超.中期因子及其与肿瘤的关系[J].临床与实验病理学杂志,1999,15(5):441-443. 被引量:27

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  • 1王志启,王建六,郭健,魏丽惠.内分泌辅助治疗子宫内膜癌的临床意义[J].中华医学杂志,2005,85(34):2414-2419. 被引量:21
  • 2原丹丹,李福琴,董春花,刘倩.中期因子在卵巢上皮性肿瘤中的表达及临床意义[J].哈尔滨医科大学学报,2006,40(6):464-466. 被引量:8
  • 3赵治国,史飞涛,周明锴,崔静,付刚,刘占举.胃癌组织中MK、VEGF表达的意义[J].世界华人消化杂志,2006,14(36):3517-3520. 被引量:7
  • 4Livak KJ,Schmittgen TD.Analysis of relative gene exression data using real 2 time quamtitative PCR and the 2 C-Delta C method.Methods,2001,25:402-408.
  • 5Jeon YT,Park IA,Kim YB,et al.Steroid receptor expressions in endometrial cancer:clinical significance and epidemiological implication.Cancer Lett,2006,239:198-204.
  • 6Ruan M,Ji T,Wu Z,et al.Evaluation of exp ression of midkine in oral squamous cell carcinoma and its correlation with tumour angiogenesis.Int J Oral Maxillofac Surg,2007,36:159-164.
  • 7Maehara H,Kaname T,Yanagi K,et al.Midkine as a novel target for antibody therapy in osteosarcoma.Biochem Biophys Res Commun,2007,358:757-762.
  • 8MURAMATSU H,SHIRAHAMA H,YONEZAWA S,et a1.Midkine,a retinoic acid-inducible growth/differentiation factor.immunochemical evidence for thefunction and distrilbution[J].Dcv Bio1,1993,159(2):392-402.
  • 9LIVAK KJ,SCHMITTGEN TD.Analysis of relative gene ex ression data using real-time quantitative PCR and the 2 (-Delta Delta C[T] ) method[J].Methods,2001,25 (4):402-408.
  • 10JEON YT,PARK IA,KIM YB,et al.Steroid receptor expressions in endometrial cancer:clinical significance and epidemiological implication[J].Cancer Lett,2006,239(2):198-204.

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