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Low and Maternal-specific Expression of p57^(KIP2) in Hydatidiform Mole and Its Clinical Implication

Low and Maternal-specific Expression of p57^(KIP2) in Hydatidiform Mole and Its Clinical Implication
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摘要 Summary: In situ hybridization was applied to locate and detect the expression of p57 KIP2 in hydatidiform mole (5 cases of partial hydatidiform mole and 18 cases of complete hydatidiform mole) and normal villi (23 cases). The positive signals of p57 KIP2 expression were analyzed by HPIAS-1000 Image-Analysis System. p57 KIP2 was highly expressed in normal villi but showed distinct low expression in hydatidiform mole (P<0.01). Furthermore, the locus of low expression of p57 KIP2 accorded with the place where lesion of trophoblast occurred. Detection of p57 KIP2 made it possible to study the genetics of hydatidiform mole at the transcriptional level. Low expression of p57 KIP2 could be a molecular marker in hydatidiform mole and a target for therapy. Summary: In situ hybridization was applied to locate and detect the expression of p57 KIP2 in hydatidiform mole (5 cases of partial hydatidiform mole and 18 cases of complete hydatidiform mole) and normal villi (23 cases). The positive signals of p57 KIP2 expression were analyzed by HPIAS-1000 Image-Analysis System. p57 KIP2 was highly expressed in normal villi but showed distinct low expression in hydatidiform mole (P<0.01). Furthermore, the locus of low expression of p57 KIP2 accorded with the place where lesion of trophoblast occurred. Detection of p57 KIP2 made it possible to study the genetics of hydatidiform mole at the transcriptional level. Low expression of p57 KIP2 could be a molecular marker in hydatidiform mole and a target for therapy.
出处 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2002年第2期121-122,157,共3页 华中科技大学学报(医学英德文版)
关键词 p57 KIP2 hydatidiform mole in situ hybridization p57 KIP2 hydatidiform mole in situ hybridization
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  • 1[1]Hartmann W, Waha A, Koch A et al. p57(KIP2) is not mutated in hepatoblastoma but shows increased tran scriptional activity in a comparative analysis of the three imprinted genes p57 (KIP2), IGF2, and H19. Am J Pathol, 2000,157(4): 1393
  • 2[2]Berek J S. Novak's Gynecology. 2th eds. Baltimore:Williams & Wilkins, 1996. 487
  • 3[3]Hatada I, Inazawa J, Abe T et al. Genomic imprinting of human p57Ku2 and its reduced expression in Wilm's tu-mors. Hum Mol Genet, 1996, 5(6): 783
  • 4[4]Kondo M, Matsuoka S, Uchida K et al. Selective mater nal-allele loss in human lung cancers of the maternally expressed p57KIP2 gene at 1 1p15.5. Oncogene, 1996,21,12(6): 1365
  • 5[5]Overall M L, Spencer J, Bakker M et al. p57K1P2 is ex-pressed in Wilms' tumor with LOH of 11p15.5. Genes Chromosomes Cancer, 1996,17(1 ): 56
  • 6[6]Hu R J, LeeM P, Johnson L Aet al. A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues. Hum Mol Genet, 1996,5(11):1743
  • 7[7]Goshen R, Ben-Rafael Z, Gonik B et al. The role of ge-nomic imprinting in implantation. Fertil Steril, 1994,62(5):903

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