메뉴 건너뛰기




Volumn 17, Issue 2, 1998, Pages 106-112

Frequent loss of chromosome 12 in human epithelial ovarian tumors: A chromosomal In situ hybridization study

Author keywords

Chromosomal in situ hybridization; Chromosome 12; Epithelial ovarian tumors

Indexed keywords

ARTICLE; CANCER DIAGNOSIS; CANCER GENETICS; CHROMOSOME 12; CHROMOSOME ANALYSIS; CHROMOSOME LOSS; CLINICAL ARTICLE; DISOMY; DNA PROBE; FEMALE; HUMAN; HUMAN TISSUE; HYSTERECTOMY; IN SITU HYBRIDIZATION; OVARY CANCER; PRIORITY JOURNAL; SALPINGOOOPHORECTOMY;

EID: 0031898929     PISSN: 02771691     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004347-199804000-00002     Document Type: Article
Times cited : (4)

References (34)
  • 1
    • 0001833641 scopus 로고
    • Surface epithelial-stromal tumors of the ovary
    • Kurman RJ (ed). New York: Springer-Verlag
    • Russel, P. Surface epithelial-stromal tumors of the ovary. In: Kurman RJ (ed). Blaustein's Pathology of the Female Genital Tract. New York: Springer-Verlag, 1994:705-82.
    • (1994) Blaustein's Pathology of the Female Genital Tract , pp. 705-782
    • Russel, P.1
  • 2
    • 0028960676 scopus 로고
    • Genetic changes in ovarian cancer
    • Pejovic T. Genetic changes in ovarian cancer. Ann Med 1995;27: 73-8.
    • (1995) Ann Med , vol.27 , pp. 73-78
    • Pejovic, T.1
  • 5
    • 0027099664 scopus 로고
    • Trisomy 12 in pediatric granulosa-stromal cell tumors
    • Schofield DE, Fletcher JA. Trisomy 12 in pediatric granulosa-stromal cell tumors. Am J Pathol 1992;141:1265-9.
    • (1992) Am J Pathol , vol.141 , pp. 1265-1269
    • Schofield, D.E.1    Fletcher, J.A.2
  • 6
    • 0025190797 scopus 로고
    • Chromosome aberrations in metastatic ovarian cancer: Relationship with abnormalities in primary tumors
    • Bello MJ, Rey JA. Chromosome aberrations in metastatic ovarian cancer: relationship with abnormalities in primary tumors. Int J Cancer 1990;45:50-4.
    • (1990) Int J Cancer , vol.45 , pp. 50-54
    • Bello, M.J.1    Rey, J.A.2
  • 9
    • 0028917494 scopus 로고
    • Centromere spreading and centromeric aberrations in ovarian tumors
    • Zhu D, Ma MS, Zhao RZ, Li MY. Centromere spreading and centromeric aberrations in ovarian tumors. Cancer Genet Cytogenet 1995;80:63-5.
    • (1995) Cancer Genet Cytogenet , vol.80 , pp. 63-65
    • Zhu, D.1    Ma, M.S.2    Zhao, R.Z.3    Li, M.Y.4
  • 11
    • 0028282920 scopus 로고
    • Clonal chromosome abnormalities in 54 cases of ovarian carcinoma
    • Thompson FH, Emerson J, Alberts D, et al. Clonal chromosome abnormalities in 54 cases of ovarian carcinoma. Cancer Genet Cytogenet 1994;73:33-45.
    • (1994) Cancer Genet Cytogenet , vol.73 , pp. 33-45
    • Thompson, F.H.1    Emerson, J.2    Alberts, D.3
  • 12
    • 0026579241 scopus 로고
    • Chromosome aberrations in 35 primary ovarian carcinomas
    • Pejovic T, Heim S, Mandahl N, et al. Chromosome aberrations in 35 primary ovarian carcinomas. Genes Chromosomes Cancer 1992;4:58-68.
    • (1992) Genes Chromosomes Cancer , vol.4 , pp. 58-68
    • Pejovic, T.1    Heim, S.2    Mandahl, N.3
  • 13
    • 0026727680 scopus 로고
    • Frequent loss of heterozygosity on chromosome Xp and 13q in human ovarian cancer
    • Yang-Feng TL, Li S, Han H, Schwartz PE. Frequent loss of heterozygosity on chromosome Xp and 13q in human ovarian cancer. Int J Cancer 1992;52:575-80.
    • (1992) Int J Cancer , vol.52 , pp. 575-580
    • Yang-Feng, T.L.1    Li, S.2    Han, H.3    Schwartz, P.E.4
  • 14
    • 0026196872 scopus 로고
    • Detection of numerical chromosomal aberrations using in situ hybridization in paraffin sections of routinely processed bladder cancers
    • Hopman AHN, Hooren van E, Kaa van de CA, Vooijs GP, Ramaekers FCS. Detection of numerical chromosomal aberrations using in situ hybridization in paraffin sections of routinely processed bladder cancers. Mod Pathol 1991;4:503-13.
    • (1991) Mod Pathol , vol.4 , pp. 503-513
    • Hopman, A.H.N.1    Van Hooren, E.2    Van De Kaa, C.A.3    Vooijs, G.P.4    Ramaekers, F.C.S.5
  • 15
    • 0025142691 scopus 로고
    • Trisomy 12 is an consistent chromosomal aberration in benign ovarian tumors
    • Pejovic T, Heim S, Mandahl N, et al. Trisomy 12 is an consistent chromosomal aberration in benign ovarian tumors. Genes Chromosomes Cancer 1990;2:48-52.
    • (1990) Genes Chromosomes Cancer , vol.2 , pp. 48-52
    • Pejovic, T.1    Heim, S.2    Mandahl, N.3
  • 16
    • 0003308295 scopus 로고
    • International histological classification and staging of tumors. No. 9
    • Geneva: World Health Organization
    • Serov SF, Scully RE, Sobin LH. International histological classification and staging of tumors. No. 9. In: Histologic Typing of Ovarian Tumors. Geneva: World Health Organization, 1973.
    • (1973) Histologic Typing of Ovarian Tumors
    • Serov, S.F.1    Scully, R.E.2    Sobin, L.H.3
  • 17
    • 0026545381 scopus 로고
    • Optimization of non-isotopic in situ hybridization of formalin-fixed, paraffin-embedded material using digoxigenin-labelled probes and transgenic tissues
    • Fleming KA, Evans M, Ryley KC, Franklin D, Lovell-Badge RH, Morey AL. Optimization of non-isotopic in situ hybridization of formalin-fixed, paraffin-embedded material using digoxigenin-labelled probes and transgenic tissues. J Pathol 1992;167:9-17.
    • (1992) J Pathol , vol.167 , pp. 9-17
    • Fleming, K.A.1    Evans, M.2    Ryley, K.C.3    Franklin, D.4    Lovell-Badge, R.H.5    Morey, A.L.6
  • 18
    • 0027390348 scopus 로고
    • Localization of plasminogen activator inhibitor-1 production in inflammed appendix by in situ mRNA hybridization
    • Whawel SA, Wang Y, Fleming KA, Thompson EM, Thompson JN. Localization of plasminogen activator inhibitor-1 production in inflammed appendix by in situ mRNA hybridization. J Urol 1993;169:67-71.
    • (1993) J Urol , vol.169 , pp. 67-71
    • Whawel, S.A.1    Wang, Y.2    Fleming, K.A.3    Thompson, E.M.4    Thompson, J.N.5
  • 21
    • 0028099486 scopus 로고
    • Fluorescent in situ hybridization in routinely processed bone marrow aspirate clot and core biopsy sections
    • Miranda RN, Mark HFL, Medeiros LF. Fluorescent in situ hybridization in routinely processed bone marrow aspirate clot and core biopsy sections. Am J Pathol 1994;145:1309-14.
    • (1994) Am J Pathol , vol.145 , pp. 1309-1314
    • Miranda, R.N.1    Mark, H.F.L.2    Medeiros, L.F.3
  • 22
    • 0023949872 scopus 로고
    • In situ hybridization as a tool to study numerical chromosome aberrations using in solid bladder tumors
    • Hopman AHN, Ramaekers FCS, Raap AK. In situ hybridization as a tool to study numerical chromosome aberrations using in solid bladder tumors. Histochemistry 1988;8:307-16.
    • (1988) Histochemistry , vol.8 , pp. 307-316
    • Hopman, A.H.N.1    Ramaekers, F.C.S.2    Raap, A.K.3
  • 23
    • 0027448202 scopus 로고
    • Interphase cytogenetics in paraffin sections of lung tumors by non-isoptopic in situ hybridization
    • Kim SY, Lee JS, Ro JY, Gay ML, Hong WK, Hittelman WN. Interphase cytogenetics in paraffin sections of lung tumors by non-isoptopic in situ hybridization. Am J Pathol 1993;142:307-17.
    • (1993) Am J Pathol , vol.142 , pp. 307-317
    • Kim, S.Y.1    Lee, J.S.2    Ro, J.Y.3    Gay, M.L.4    Hong, W.K.5    Hittelman, W.N.6
  • 25
    • 0028234259 scopus 로고
    • Thick-section fluorescence in situ hybridization on formalin-fixed, paraffin-embedded archival tissue provides a histogenetic profile
    • Thompson CT, Leboit PE, Nederlof PM, Gray JW. Thick-section fluorescence in situ hybridization on formalin-fixed, paraffin-embedded archival tissue provides a histogenetic profile. Am J Pathol 1994:144:237-43.
    • (1994) Am J Pathol , vol.144 , pp. 237-243
    • Thompson, C.T.1    Leboit, P.E.2    Nederlof, P.M.3    Gray, J.W.4
  • 27
    • 0026458680 scopus 로고
    • Verification of isochromosome 12p and identification of other chromosome 12 aberrations in gonadal and extragonadal human germ cell tumors by bicolor double fluorescence in situ hybridization
    • Suijkerbuijk RF, Looijenga L, de Jong B, Oosterhuis JW, Cassiman JJ, Geurts van Kessel A. Verification of isochromosome 12p and identification of other chromosome 12 aberrations in gonadal and extragonadal human germ cell tumors by bicolor double fluorescence in situ hybridization. Cancer Genet Cytogenet 1992;63: 8-16.
    • (1992) Cancer Genet Cytogenet , vol.63 , pp. 8-16
    • Suijkerbuijk, R.F.1    Looijenga, L.2    De Jong, B.3    Oosterhuis, J.W.4    Cassiman, J.J.5    Van Geurts Kessel, A.6
  • 28
    • 0028142025 scopus 로고
    • Evaluation of 20 archival prostate tumor specimens by fluorescence in situ hybridization (FISH)
    • Brothman AR, Watson MJ, Zhu XL, Williams BJ, Rohr LR. Evaluation of 20 archival prostate tumor specimens by fluorescence in situ hybridization (FISH). Cancer Genet Cytogenet 1994; 75:40-4.
    • (1994) Cancer Genet Cytogenet , vol.75 , pp. 40-44
    • Brothman, A.R.1    Watson, M.J.2    Zhu, X.L.3    Williams, B.J.4    Rohr, L.R.5
  • 30
    • 0028961450 scopus 로고
    • Translocation t(12;16)(q13′1) in myxoid liposarcoma and round cell liposarcoma: Molecular and cytogenetic analysis
    • Knight JC, Renwick PJ, Dal Cin P, van den Berghe H, Fletcher CDM. Translocation t(12;16)(q13′1) in myxoid liposarcoma and round cell liposarcoma: Molecular and cytogenetic analysis. Cancer Res 1995;55:24-7.
    • (1995) Cancer Res , vol.55 , pp. 24-27
    • Knight, J.C.1    Renwick, P.J.2    Dal Cin, P.3    Van Den Berghe, H.4    Fletcher, C.D.M.5
  • 31
    • 0028949488 scopus 로고
    • Identification of a YAC spanning the translocation breakpoints in uterial leiomyomata, pulmonary chondroid hamartoma, and lipoma: Physical mapping of the 12q14-q15 breakpoint region in uterine leiomyomata
    • Fejzo MS, Yoon SJ, Montgomery KT, et al. Identification of a YAC spanning the translocation breakpoints in uterial leiomyomata, pulmonary chondroid hamartoma, and lipoma: physical mapping of the 12q14-q15 breakpoint region in uterine leiomyomata. Genomics 1995;26:265-71.
    • (1995) Genomics , vol.26 , pp. 265-271
    • Fejzo, M.S.1    Yoon, S.J.2    Montgomery, K.T.3
  • 32
    • 0028853347 scopus 로고
    • Identification of the chromosome 12 translocation breakpoint region of a pleiomorphic salivary gland adenoma with t(1;12)(p22;q15) as the sole cytogenetic abnormality
    • Kools PF, Wanschura S, Schoenmakers EF, et al. Identification of the chromosome 12 translocation breakpoint region of a pleiomorphic salivary gland adenoma with t(1;12)(p22;q15) as the sole cytogenetic abnormality. Cancer Gener Cytogenet 1995;79:1-7.
    • (1995) Cancer Gener Cytogenet , vol.79 , pp. 1-7
    • Kools, P.F.1    Wanschura, S.2    Schoenmakers, E.F.3
  • 33
    • 0028986932 scopus 로고
    • P27Kip1: Chromosomal mapping to 12p12-12p13.1 and abscence of mutation in human tumors
    • Ponce-Castaneda MV, Lee MH, Latres E, et al. p27Kip1: Chromosomal mapping to 12p12-12p13.1 and abscence of mutation in human tumors. Cancer Res 1995;55:1211-1214.
    • (1995) Cancer Res , vol.55 , pp. 1211-1214
    • Ponce-Castaneda, M.V.1    Lee, M.H.2    Latres, E.3
  • 34
    • 0028239486 scopus 로고
    • Suppression of tumorigenicity of human prostate cancer cell by introduction of human chromosome del(12)(q13)
    • Berube NG, Speevak MD, Chevrette M. Suppression of tumorigenicity of human prostate cancer cell by introduction of human chromosome del(12)(q13). Cancer Res 1994;54:3077-81.
    • (1994) Cancer Res , vol.54 , pp. 3077-3081
    • Berube, N.G.1    Speevak, M.D.2    Chevrette, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.