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P16 P15及VEGF蛋白在原发性卵巢癌中的表达及临床意义 被引量:7

Expression and clinical significance of P16, P15,and VEGF proteins in primary epithelial ovarian carcinoma
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摘要 目的:探讨P16、P15及血管内皮生长因子(VEGF)在原发性卵巢癌中表达情况及其与临床病理特征的关系。方法:采用免疫组织化学S-P法对170例原发性卵巢癌、60例交界性肿瘤及60例良性肿瘤组织进行P16、P15和VEGF蛋白检测。结果:P16在卵巢癌的表达率为40.0%(68/170),明显低于良性肿瘤组65.0%(39/60)和交界性肿瘤组56.7%(34/60)(P<0.05);P15在卵巢癌组的阳性表达率为45.3%(77/170),显著低于良性肿瘤组68.3%、交界性肿瘤组61.7%(37/60)(P<0.05);VEGF在卵巢癌组的阳性表达率为71.2%(14/170),明显高于良性肿瘤组45.0%(27/60)和交界性肿瘤组53.3%(32/60)(P<0.05)。在卵巢癌组中,P16和P15表达呈正相关(r=0.294,P<0.01),VEGF与P16和P15的表达呈负相关(r值分别为-0.461和-0.251,P<0.01)。三者表达强度与肿瘤分化程度、临床分期、淋巴结转移有显著相关性,肿瘤分化越低、临床分期越高、淋巴结转移者P16、P15阳性表达率越低(P<0.05),VEGF阳性表达率越高(P<0.05)。P16和P15的表达与有无脉管瘤栓无关,VEGF在有脉管瘤栓组的表达高于无脉管瘤栓组。结论:P16和P15的低表达与VEGF蛋白高表达在卵巢癌的发展过程中可能起协同作用,共同促进卵巢癌的恶性发展进程。 Objective:The present study aimed to investigate the expressions of P16, P15, and vascular endothelial growth factor (VEGF) in primary epithelial ovarian carcinoma as well as their relationship with clinicopathological features. Methods:P16, P15, and VEGF proteins were detected in 170 cases of primary epithelial ovarian carcinoma, 60 cases of borderline tumors, and 60 cases of benign tumors by using S-P immunohistochemical staining method. Result:In ovarian carcinoma, the positive expression rate of P16 was 40.0%. This rate was lower than that in benign tumors (65.0%) and borderline tumors (56.7%;P〈0.05). In epithelial ovarian carcinoma, the positive expression rate of P15 was 45.3%. This rate was also lower than that in benign tumors (68.3%) and borderline tumors (61.7%;P〈0.05). In epithelial ovarian carcinoma, the positive expression rate of VEGF was 71.2%. This was higher than that in benign tumors (45.0%) and borderline tumors (53.3%;P〈0.05). In ovarian carcinoma, P16 expression was positively correlated with P15 (r=0.294;P〈0.01), but VEGF expression was negatively correlated with P16 and P15 (r=-0.461;r=-0.251;P〈0.01). The expressions of these three proteins were significantly correlated with the degree of tumor differentiation, clinical stage, and lymph node metastasis. In lymph node metastasis, high clinical stage, or poor differentiation, low positive rates of P16 and P15 were observed (P〈0.05). For VEGF, the positive rate was high. P16 and P15 expressions were not correlated with vascular invasion. VEGF expression was higher in the vascular invasion group than in the non-vascular invasion group. Conclusion:Low P16 and P15 expressions as well as high VEGF expression may exhibit synergistic effects on the development of ovarian carcinoma and simultaneously promote malignant development of ovarian carcinoma.
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2013年第9期521-524,共4页 Chinese Journal of Clinical Oncology
关键词 卵巢肿瘤 P16 P15 VEGF 免疫组织化学 ovarian tumor, P 16, P 15, VEGF, immunohistochemistry
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参考文献15

  • 1Siegel R, Ward E, Brawley O, et al. Cancer statistics, 2011: the im-pact of eliminating socioeconomic and racial disparities on prema-ture cancer deaths Q]. CA Cancer J Clin, 2011,61(4) :212-236.
  • 2Jemal A, Siegel R, Xu J, et al. Cancer statistics, 2010[J]. CA CancerJGlin, 2010, 60(5):277-300.
  • 3Kamb A, Gruis NA, Weaver—Feldhaus J, et al. A cell cycle regula-tor potentially involved in genesis of many tumor types[]]. Science,1994, 264(5157):436-440.
  • 4Lee MH, Yang HY. Negative regulators of cyclin—dependent kinas-es and their roles in cancers [J]. Cell Mol Life Sci, 2001, 58(12—13):1907-1922.
  • 5Larsen CJ. Contribution of the dual coding capacity of thepi 6INK4a/MTS 1/CDKN2 locus to human malignancies [J]. ProgCell Cycle Res, 1997, 3:109—124.
  • 6Jha AK, Nikbakht M, Jain V, et al. pl6(INK4a) and pl5(INK4b)gene promoter methylation in cervical cancer patients [J]. OncolLett, 2012,3(6):1331-1335.
  • 7Ko E, Kim Y, Kim SJ, et al. Promoter hypermethylation of the pl6gene is associated with poor prognosis in recurrent early—stage he-patocellular carcinomaj]. Cancer Epidemiol Biomarkers Prev, 2008,17(9):2260-2267.
  • 8Li G, Ji Y, Liu C, et al. Reduced levels of pl5INK4b, pl6INK4a,p21cipl and p27kipl in pancreatic carcinoma[J]. Mol Med Rep,2012,5(4):1106-1110.
  • 9Bai P, Xiao X, Zou J, et al. Expression of pl4(ARF), pl5(INK4b),pl6(INK4a) and skp2 increases during esophageal squamous cellcancer progression[J]. Exp Ther Med, 2012, 3(6):1026-1032.
  • 10Surowiak P, Materna V,Maciejczyk A, et al. Decreased expressionof pi6 in ovarian cancers represents an unfavourable prognostic fac-tor]]]. Histol Histopathol, 2008, 23 (5):531-538.

同被引文献70

  • 1王喜梅,刘逢吉,湛丽,孙雷,郑仁恕,张众.子宫颈腺癌中HPV16/18感染对p16^(Ink4a)、Rb蛋白表达的影响[J].临床与实验病理学杂志,2006,22(3):320-324. 被引量:5
  • 2郑金锋,马淑芳,耿明,曹永成,刘莹.p16和p15及PCNA在子宫颈癌组织中的表达及临床病理意义[J].中华肿瘤防治杂志,2007,14(4):291-293. 被引量:15
  • 3杨吉成 宋礼华 周建华.医用细胞工程[M].上海:上海交通大学出版社,2001.92.
  • 4Syroid DE, Mayeox PR, Burrola PG, et al. Cell death in theSchwann cell lineage and its regulation byneuregulin [J]. Proc Natl Acad Sci USA, 1996,93( 17):9229-9234.
  • 5Hess C J, Errami A, BerkhofJ, et al. Con- current methylation of promoters from tumor associated genes predicts outcome in acute myeloid leukemia[J]. Leuk Ly- mphoma, 2008, 49(6): 1132-1141.
  • 6Takeshima M, Saitoh M, Kusano K, et al. High frequency of hypermethylation of p14, p15 and p16 in oral precan cerous lesions associated with betelquid chewing in Sri Lanka[J]. J Oral Pathol Med, 2008, 37(8):475-479.
  • 7JHA A K, NIKBAKHT M, JAIN V,et al. pl6(INK4a) and pl5(INK4b) gene promoter methylation in cervical cancer patients[J]. Oncol Lett, 2012, 3(6) : 1331 - 1335.
  • 8KO E, KIM Y, KIM S J, et al. Promoter hypermethylation of thepi 6 gene is associated with poor prognosis in recurrent early - stagehepatocellular carcinoma[ J]. Cancer Epidemiol Biomarkers Prev,2008,17(9) : 2260 -2267.
  • 9U G, JI Y,LIU C,et al. Reduced levels of pl5INK4b,pl6INK4a, p21cipl and p27kipl in pancreatic carcinoma [ J ].Mol Med Rep, 2012, 5(4) : 1106-1110.
  • 10BAI P, XIAO X,ZOU J,et al. Expression of pl4(ARF),pl5(INK4b) , pl6 ( INK4a) and skp2 increases during esophagealsquamous cellcancer progression [ J ]. Exp Ther Med, 2012,3(6): 1026 -1032.

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