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PTEN和FHIT在上皮性卵巢肿瘤中的表达及其临床意义 被引量:7

Expression levels and clinical significance of PTEN and FHIT in epithelial ovarian tumors
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摘要 目的:探讨PTEN和FHIT蛋白在上皮性卵巢肿瘤中的表达及意义。方法:收集该院85例上皮性卵巢肿瘤的妇科手术石蜡标本(51例卵巢癌、16例卵巢交界性肿瘤、18例卵巢良性肿瘤),另收集同期其他条件类似的10例正常卵巢组织作对照,采用免疫组织化学SP法检测组织中FHIT和PTEN表达。结果:FHIT在10例正常卵巢组织、18例良性上皮性卵巢肿瘤和16例交界性肿瘤中均呈阳性表达,在上皮性卵巢癌中,其阴性表达率(37.3%,19/51)明显高于良性卵巢肿瘤和交界性卵巢肿瘤,其差异均有统计学意义(P<0.05)。FHIT蛋白阴性表达率在伴淋巴结转移组和不伴淋巴结转移组比较差异也有统计学意义(P<0.05);FHIT蛋白的阴性表达率与病理类型及临床分期无关。卵巢交界性肿瘤和卵巢癌组织中PTEN蛋白表达显著低于卵巢良性肿瘤和正常卵巢组织,其差异均有统计学意义(P<0.05);PTEN蛋白表达与卵巢癌组织分化程度呈正相关(P<0.01),与临床病理分期负相关(P<0.05)。结论:PTEN基因和FHIT基因表达降低或缺失在卵巢癌的发生、侵袭和转移中可能起重要作用,PTEN和FHIT联合检测有助于卵巢肿瘤的早期诊断、早期治疗及生物学行为的评估。 Objective: To explore the expression levels and clinical significance of PTEN and FHIT in epithelial ovarian tumors. Methods: Surgical specimens in paraffin of 95 cases (51 cases of ovarian cancer, 16 cases of borderline ovarian tumor, 18 cases of benign ovarian tumors, 10 cases of normal ovarian tissue) were collected, the expression levels of FHIT and PTEN were detected by immunohistochemical SP method. Results: FHIT expressed in 10 cases of normal ovarian tissue, 18 cases of benign ovarian tumor and 16 cases of borderline ovarian tumor, the negative expression rate in ovarian cancer was significantly higher than those in benign ovariar/tumor and borderline ovarian tumor ( P 〈 0. 05 ) . There was significant difference in negative expression rate of FHIT protein between lymphatic metastasis group and non - lymphatic metastasis group ( P 〈 0. 05 ) ; negative expression rate of FHIT protein was not related to pathological types and clinical staging. The expression levels of PTEN protein in borderline ovarian tumor and ovarian cancer were significantly lower than those in benign ovarian tumor and normal ovarian tissue ( P 〈 0. 05 ) . There was a positive correlation between PTEN protein expression and differentiation grades of ovarian cancer (P 〈 0. 01 ), and there was a negative correlation between PTEN protein expression and clinical pathological staging ( P 〈 0. 05 ) . Conclusion : Low expression levels and expression deletion of PTEN gene and FHIT gene play an important role in the oncogenesis, invasion and metastasis of ovarian cancer, combined detection of PTEN and FHIT contribute to early diagnosis, early treatment and assessment of biological behaviors.
出处 《中国妇幼保健》 CAS 北大核心 2010年第5期654-656,共3页 Maternal and Child Health Care of China
基金 广东省深圳市福田区公益性科研项目〔FTWS001〕
关键词 卵巢癌 PTEN FHIT 免疫组织化学 Ovarian cancer PTEN FHIT Immunohistochemistry
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参考文献9

  • 1Steck PA, Pershouse MA, Jasse SA et al. Identification of a candidate tumour suppressor gene, MMACI at chromosome 10q23.3 that is mutated in multple advanced cancer [J].NatGenet, 1997, 15 (4) : 356.
  • 2Ohta M, Inoue H, Cotticelli MG et al. The human FHIT gene, spanning the ehromosome 3P14.2 fragile site and renal cell carcinoma associated transloeation breakpoint, is abnormal in digestive tract cancer [J]. Cell, 1996, 84:587.
  • 3Hao XP, Willis JE, Pretlow TG et al. Loss of fragile histidine triad expression in coloretal carcinomas and premalignant lesions [J]. Cancer Res, 2000, 60 (1): 18.
  • 4Downes CP, Perera N, Ross Set al. Substrate specificity and acute regulation of the tumour suppressor phosphatase, PTEN[J].Biochem SocSymp, 2007, 7d (1): 69.
  • 5Kurose R, Zhou XP, Araki T et al. Frequent loss of PTEN expression in linked to elevated phosphorylated Alt levels, but not associated with p27 and cyelin D1 expression, in primary epithelial ovarian carcinomas [J]. Am J Pathol, 2001 , 158:2097.
  • 6Schondorf T, Ebert MP. Hypermethylation of the PTEN gene in ovarian cancer lins[J]. Cancer Let, 2004, 207 (2) : 215.
  • 7Chang KW, Kao SY, Tzeng RJ et al. Multiple molecular alterations of FHIT in beta- associated oral carcinoma [ J] . Pathol, 2002, 196 (3) : 300.
  • 8Zochbauer - Muller S, Fong KM, Maitra A el al. 5CpG island methylation of the FHIT gene is correlated with loss of gene expression in lung and breast cancer [J]. Cancer Res, 2001, 61 (9) : 3581.
  • 9张淑红,张向宁.脆性位点抑癌基因FHIT和WWOX蛋白与卵巢上皮癌的相关性[J].实用医药杂志,2008,25(7):786-789. 被引量:10

二级参考文献6

  • 1Paige A J, Taylor K J, Taylor C, et al. WWOX:a candidate tumor suppressor gene involoved in multiple tumor types. Proc natl Acad Sci, 2001,98:11417.
  • 2Krummel K, Denison S, Calhoun E, et al. The common fragile site FRA16D and its associated gene WWOX are highly conserved in the mouse at FRa8El. Genes Chrom Cancer, 2002, 34:154.
  • 3Bednerek AK, Laflin K J, Daniel RL, et al. WWOX,a novel WW domain - containing protein mapping to human chromosome 16q^23.3-24.1, a region frenquently affected in breast cancer. Cancer Res, 2000,60(8):2140.
  • 4Maitra A, Wistuber Ⅱ, Washington C, et al. High-resolution chromosome 3p alletotyping of breast carcinomas and precursur lesions denmonstrates frequent loss of heterozigosity and discontinuous pattern of allele loss. Im J Pathol, 2001,159(1):119.
  • 5Kannan K, Munirajan A.K, Bhuvarahamurthy V, et al. FHIT gene mutations and single nucleotide polymorphism in Indian oral and cervical squamous cell carcinomas. Oral Oncology, 2000,36:189.
  • 6Croce CM, Sozzi Gand Huebner K. Role of FHIT in human cancer. J Clin Oncol, 1999,17(5):1618.

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