메뉴 건너뛰기




Volumn 33, Issue 9, 2002, Pages 910-914

Renal cell carcinoma: Allelic loss at chromosome 9 using the fluorescent multiplex-polymerase chain reaction technique

Author keywords

Chromosome 9; Loss of heterozygosity; Nuclear grade; Renal cell carcinoma; Tumor stage

Indexed keywords

DNA;

EID: 0036742816     PISSN: 00468177     EISSN: None     Source Type: Journal    
DOI: 10.1053/hupa.2002.126877     Document Type: Article
Times cited : (10)

References (34)
  • 1
    • 0028790326 scopus 로고
    • Terminal deletion of chromosome 3p sequences in nonpapillary renal cell carcinomas: A breakpoint cluster between loci D3S1285 and D3S1603
    • Wilhelm M, Bugert P, Kenck C, et al: Terminal deletion of chromosome 3p sequences in nonpapillary renal cell carcinomas: A breakpoint cluster between loci D3S1285 and D3S1603. Cancer Res 55:5383-5385, 1995
    • (1995) Cancer Res , vol.55 , pp. 5383-5385
    • Wilhelm, M.1    Bugert, P.2    Kenck, C.3
  • 2
    • 0027954044 scopus 로고
    • Mutations of the VHL tumour suppressor gene in renal carcinoma
    • Gnarra JR, Tory K, Weng Y, et al: Mutations of the VHL tumour suppressor gene in renal carcinoma. Nat Gen 7:85-90, 1994
    • (1994) Nat Gen , vol.7 , pp. 85-90
    • Gnarra, J.R.1    Tory, K.2    Weng, Y.3
  • 3
    • 0029944971 scopus 로고    scopus 로고
    • Mutation of the VHL gene is associated exclusively with the development of non-papillary renal cell carcinomas
    • Kenck C, Wilhelm M, Bugert P, et al: Mutation of the VHL gene is associated exclusively with the development of non-papillary renal cell carcinomas. J Pathol 179:157-161, 1996
    • (1996) J Pathol , vol.179 , pp. 157-161
    • Kenck, C.1    Wilhelm, M.2    Bugert, P.3
  • 4
    • 0025975990 scopus 로고
    • Allelotype of renal cell carcinoma
    • Morita R, Ishikawa J, Tsutsumi M, et al: Allelotype of renal cell carcinoma. Cancer Res 51:820-823, 1991
    • (1991) Cancer Res , vol.51 , pp. 820-823
    • Morita, R.1    Ishikawa, J.2    Tsutsumi, M.3
  • 5
    • 0027258065 scopus 로고
    • Tumor suppressor gene allelic loss in human renal cancers
    • Brooks JD, Bova GS, Marshall FF, et al: Tumor suppressor gene allelic loss in human renal cancers. J Urol 150:1278-1283, 1993
    • (1993) J Urol , vol.150 , pp. 1278-1283
    • Brooks, J.D.1    Bova, G.S.2    Marshall, F.F.3
  • 6
    • 0028091126 scopus 로고
    • Molecular genetic investigation of sporadic renal cell carcinoma: Analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22
    • Foster K, Crossey PA, Cairns P, et al: Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22. Br J Cancer 69:230-234, 1994
    • (1994) Br J Cancer , vol.69 , pp. 230-234
    • Foster, K.1    Crossey, P.A.2    Cairns, P.3
  • 7
    • 0025017058 scopus 로고
    • Allelic losses of chromosomes 9, 11, and 17 in human bladder cancer
    • Tsai YC, Nichols PW, Hiti AL, et al: Allelic losses of chromosomes 9, 11, and 17 in human bladder cancer. Cancer Res 50:44-47, 1990
    • (1990) Cancer Res , vol.50 , pp. 44-47
    • Tsai, Y.C.1    Nichols, P.W.2    Hiti, A.L.3
  • 8
    • 0027516042 scopus 로고
    • Initiation of bladder cancer may involve deletion of a tumour-suppressor gene on chromosome 9
    • Cairns P, Shaw ME, Knowles MA: Initiation of bladder cancer may involve deletion of a tumour-suppressor gene on chromosome 9. Oncogene 8:1083-1085, 1993
    • (1993) Oncogene , vol.8 , pp. 1083-1085
    • Cairns, P.1    Shaw, M.E.2    Knowles, M.A.3
  • 9
    • 0028158767 scopus 로고
    • Frequent loss of chromosome 9 in human primary non-small cell lung cancer
    • Merlo A, Gabrielson E, Askin F, et al: Frequent loss of chromosome 9 in human primary non-small cell lung cancer. Cancer Res 54:640-642, 1994
    • (1994) Cancer Res , vol.54 , pp. 640-642
    • Merlo, A.1    Gabrielson, E.2    Askin, F.3
  • 10
    • 0026627965 scopus 로고
    • Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
    • Gailani MR, Bale SJ, Leffell DJ, et al: Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9. Cell 69:111-117, 1992
    • (1992) Cell , vol.69 , pp. 111-117
    • Gailani, M.R.1    Bale, S.J.2    Leffell, D.J.3
  • 11
    • 0028008679 scopus 로고
    • Progression of basal cell carcinoma through loss of chromosome 9q and inactivation of a single p53 allele
    • van der Riet P, Karp D, Farmer E, et al: Progression of basal cell carcinoma through loss of chromosome 9q and inactivation of a single p53 allele. Cancer Res 54:25-27, 1994
    • (1994) Cancer Res , vol.54 , pp. 25-27
    • Van der Riet, P.1    Karp, D.2    Farmer, E.3
  • 12
    • 0031881427 scopus 로고    scopus 로고
    • Mutations in the human homologue of the Drosophila patched gene in esophageal squamous cell carcinoma
    • Maesawa C, Tamura G, Iwaya T, et al: Mutations in the human homologue of the Drosophila patched gene in esophageal squamous cell carcinoma. Genes Chromosomes Cancer 21:276-279, 1998
    • (1998) Genes Chromosomes Cancer , vol.21 , pp. 276-279
    • Maesawa, C.1    Tamura, G.2    Iwaya, T.3
  • 13
    • 0031036694 scopus 로고    scopus 로고
    • Sporadic medulloblastomas contain PTCH mutations
    • Raffel C, Jenkins RB, Frederick L, et al: Sporadic medulloblastomas contain PTCH mutations. Cancer Res 57:842-845, 1997
    • (1997) Cancer Res , vol.57 , pp. 842-845
    • Raffel, C.1    Jenkins, R.B.2    Frederick, L.3
  • 14
    • 15644373337 scopus 로고    scopus 로고
    • Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors
    • Xie J, Johnson RL, Zhang X, et al: Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors. Cancer Res 57:2369-2372, 1997
    • (1997) Cancer Res , vol.57 , pp. 2369-2372
    • Xie, J.1    Johnson, R.L.2    Zhang, X.3
  • 15
    • 0031717394 scopus 로고    scopus 로고
    • Dinucleotide repeat polymorphism within the tumor suppressor gene PTCH at 9q22
    • Louhelainen J, Lindstrom E, Hemminki K, et al: Dinucleotide repeat polymorphism within the tumor suppressor gene PTCH at 9q22. Clin Genet 54:239-241, 1998
    • (1998) Clin Genet , vol.54 , pp. 239-241
    • Louhelainen, J.1    Lindstrom, E.2    Hemminki, K.3
  • 19
    • 0028868209 scopus 로고
    • Localization of tumor suppressor loci on chromosome 9 in primary human renal cell carcinomas
    • Cairns P, Tokino K, Eby Y, et al: Localization of tumor suppressor loci on chromosome 9 in primary human renal cell carcinomas. Cancer Res 55:224-227, 1995
    • (1995) Cancer Res , vol.55 , pp. 224-227
    • Cairns, P.1    Tokino, K.2    Eby, Y.3
  • 20
    • 0030848639 scopus 로고    scopus 로고
    • Loss of heterozygosity at chromosomes 8p, 9p, and 14q is associated with stage and grade of non-papillary renal cell carcinomas
    • Schullerus D, Herbers J, Chudek J, et al: Loss of heterozygosity at chromosomes 8p, 9p, and 14q is associated with stage and grade of non-papillary renal cell carcinomas. J Pathol 183:151-155, 1997
    • (1997) J Pathol , vol.183 , pp. 151-155
    • Schullerus, D.1    Herbers, J.2    Chudek, J.3
  • 21
    • 0034746254 scopus 로고    scopus 로고
    • CDKNA2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas: Evidence for a second tumor suppressor gene proximal to CDKN2A
    • Schraml P, Struckmann K, Bednar R, et al: CDKNA2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas: Evidence for a second tumor suppressor gene proximal to CDKN2A. Am J Pathol 158:593-601, 2001
    • (2001) Am J Pathol , vol.158 , pp. 593-601
    • Schraml, P.1    Struckmann, K.2    Bednar, R.3
  • 22
    • 0032878968 scopus 로고    scopus 로고
    • Characteristic loss of heterozygosity in chromosome 3P and low frequency of replication errors in sporadic renal cell carcinoma
    • Chino K, Esumi M, Ishida H, et al: Characteristic loss of heterozygosity in chromosome 3P and low frequency of replication errors in sporadic renal cell carcinoma. J Urol 162:614-618, 1999
    • (1999) J Urol , vol.162 , pp. 614-618
    • Chino, K.1    Esumi, M.2    Ishida, H.3
  • 23
    • 0034322262 scopus 로고    scopus 로고
    • Genetic alterations in metastatic renal cell carcinoma detected by comparative genomic hybridization: Correlation with clinical and histological data
    • Junker K, Moravek P, Podhola M, et al: Genetic alterations in metastatic renal cell carcinoma detected by comparative genomic hybridization: Correlation with clinical and histological data. Int J Oncol 17:903-908, 2000
    • (2000) Int J Oncol , vol.17 , pp. 903-908
    • Junker, K.1    Moravek, P.2    Podhola, M.3
  • 24
    • 0029091503 scopus 로고
    • Frequency of homozygous deletion at p16/CDKN2 in primary human tumours
    • Cairns P, Polascik TJ, Eby Y, et al: Frequency of homozygous deletion at p16/CDKN2 in primary human tumours. Nat Genet 11:210-212, 1995
    • (1995) Nat Genet , vol.11 , pp. 210-212
    • Cairns, P.1    Polascik, T.J.2    Eby, Y.3
  • 25
    • 0026483716 scopus 로고
    • Homozygous deletions within human chromosome band 9p21 in melanoma
    • Fountain JW, Karayiorgou M, Ernstoff MS, et al: Homozygous deletions within human chromosome band 9p21 in melanoma. Proc Nat Acad Sci USA 89:10557-10561, 1992
    • (1992) Proc Nat Acad Sci USA , vol.89 , pp. 10557-10561
    • Fountain, J.W.1    Karayiorgou, M.2    Ernstoff, M.S.3
  • 26
    • 0343674751 scopus 로고    scopus 로고
    • Allelic loss at the D9S171 locus on chromosome 9p13 is associated with progression of papillary renal cell carcinoma
    • Schraml P, Muller D, Bednar R, et al: Allelic loss at the D9S171 locus on chromosome 9p13 is associated with progression of papillary renal cell carcinoma. J Pathol 190:457-461, 2000
    • (2000) J Pathol , vol.190 , pp. 457-461
    • Schraml, P.1    Muller, D.2    Bednar, R.3
  • 27
    • 15844386165 scopus 로고    scopus 로고
    • Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome
    • Hahn H, Wicking C, Zaphiropoulous PG, et al: Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell 85:841-851, 1996
    • (1996) Cell , vol.85 , pp. 841-851
    • Hahn, H.1    Wicking, C.2    Zaphiropoulous, P.G.3
  • 28
    • 15844381336 scopus 로고    scopus 로고
    • Human homolog of patched, a candidate gene for the basal cell nervus syndrome
    • Johnson RL, Rothman AL, Xie J, et al: Human homolog of patched, a candidate gene for the basal cell nervus syndrome. Science 272:1668-1671, 1996
    • (1996) Science , vol.272 , pp. 1668-1671
    • Johnson, R.L.1    Rothman, A.L.2    Xie, J.3
  • 29
    • 0030239754 scopus 로고    scopus 로고
    • Is human patched the gatekeeper of common skin cancers?
    • letter; comment
    • Sidransky D: Is human patched the gatekeeper of common skin cancers? [letter; comment]. Nat Genet 14:7-8, 1996
    • (1996) Nat Genet , vol.14 , pp. 7-8
    • Sidransky, D.1
  • 30
    • 0030990735 scopus 로고    scopus 로고
    • Human patched (PTCH) mRNA is overexpressed consistently in tumor cells of both familial and sporadic basal cell carcinoma
    • Unden AB, Zaphiropoulos PG, Bruce K, et al: Human patched (PTCH) mRNA is overexpressed consistently in tumor cells of both familial and sporadic basal cell carcinoma. Cancer Res 57: 2336-2340, 1997
    • (1997) Cancer Res , vol.57 , pp. 2336-2340
    • Unden, A.B.1    Zaphiropoulos, P.G.2    Bruce, K.3
  • 31
    • 1842330252 scopus 로고    scopus 로고
    • Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: Support for a gatekeeper mechanism in skin tumorigenesis
    • Vorechovsky I, Unden AB, Sandstedt B, et al: Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: Support for a gatekeeper mechanism in skin tumorigenesis. Cancer Res 57:4677-4681, 1997
    • (1997) Cancer Res , vol.57 , pp. 4677-4681
    • Vorechovsky, I.1    Unden, A.B.2    Sandstedt, B.3
  • 32
    • 0030913169 scopus 로고    scopus 로고
    • Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched
    • Pietsch T, Waha A, Koch A, et al: Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched. Cancer Res 57:2085-2088, 1997
    • (1997) Cancer Res , vol.57 , pp. 2085-2088
    • Pietsch, T.1    Waha, A.2    Koch, A.3
  • 33
    • 0030738693 scopus 로고    scopus 로고
    • Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system
    • Wolter M, Reifenberger J, Sommer C, et al: Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system. Cancer Res 57:2581-2585, 1997
    • (1997) Cancer Res , vol.57 , pp. 2581-2585
    • Wolter, M.1    Reifenberger, J.2    Sommer, C.3
  • 34
    • 0030874617 scopus 로고    scopus 로고
    • Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours
    • Vorechovsky I, Tingby O, Hartman M, et al: Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours. Oncogene 15:361-366, 1997
    • (1997) Oncogene , vol.15 , pp. 361-366
    • Vorechovsky, I.1    Tingby, O.2    Hartman, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.