PCOLCE deletion and expression analyses in uterine leiomyomata

Cancer Genetics and Cytogenetics

Volumn 137, Issue 2, 2002, Pages 133-137

  Ligon, Azra H ^a,b   Scott, Ian C ^c   Takahara, Kazuhiko ^c   Greenspan, Daniel S ^c   Morton, Cynthia C ^a  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 7; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FLUORESCENCE; GENE DELETION; GENE EXPRESSION; GENE MAPPING; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; KARYOTYPE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; UTERUS MYOMA;

EXTRACELLULAR MATRIX PROTEINS; FEMALE; GENE DELETION; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, NEOPLASTIC; GLYCOPROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LEIOMYOMA; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER; UTERINE NEOPLASMS;

EID: 0036752172     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(02)00547-2     Document Type: Article

References (20)

1. Cramer S.F., Patel A. The frequency of uterine leiomyomas. Am J Clin Pathol. 94:1990;435-438.
2. Nilbert M., Heim S. Uterine leiomyoma cytogenetics. Genes Chromosomes Cancer. 2:1990;3-13.
3. Rein M.S., Friedman A.J., Barbieri R.L., Pavelka K., Fletcher J.A., Morton C.C. Cytogenetic abnormalities in uterine leiomyomata. Obstet Gynecol. 77:1991;923-926.
4. Schoenberg Fejzo M., Yoon S.-J., Montgomery K.T., Rein M.S., Weremowicz S., Krauter K.S., Dorman T.E., Fletcher J.A., Mao J.-I., Moir D.T., Kucherlapati R.S., Morton C.C. Identification of a YAC spanning the translocation breakpoints in uterine leiomyomata, pulmonary chondroid hamartoma, and lipoma. physical mapping of the 12q14-15 breakpoint region in uterine leiomyomata Genomics. 26:1995;265-271.
5. Kazmierczak B., Bol S., Wanschura S., Bartnitzke S., Bullerdiek J. PAC clone containing the HMGI(Y) gene spans the breakpoint of a 6p21 translocation in a uterine leiomyoma cell line. Genes Chromosomes Cancer. 17:1996;191-193.
6. Hess J.L. Chromosomes translocation in benign tumors. the HMGI proteins Am J Clin Pathol. 109:1998;251-261.
7. Sargent M.S., Weremowicz S., Rein M.S., Morton C.C. Translocations in 7q22 define a critical region in uterine leiomyomata. Cancer Genet Cytogenet. 77:1994;65-68.
8. Takahara K., Kessler E., Biniaminov L., Brusel M., Eddy R.L., Jani-Sait S., Shows T.B., Greenspan D.S. Type I procollagen COOH-terminal proteinase enhancer protein. identification, primary structure, and chromosomal localization of the cognate human gene (PCOLCE) J Biol Chem. 269:1994;26280-26285.
9. Kessler E., Adar R. Type I procollagen C-proteinase from mouse fibroblasts. Purification and demonstration of a 55-kDa enhancer glycoprotein. Eur J Biochem. 186:1989;115-121.
10. Scott I.C., Clark T.G., Takahara K., Hoffman G.G., Greenspan D.S. Structural organization and expression patterns of the human and mouse genes for the type I procollagen COOH-terminal proteinase enhancer protein. Genomics. 55:1999;229-234.
11. Masuda M., Igarashi H., Kano M., Yoshikura H. Effects of procollagen C-proteinase enhancer protein on the growth of cultured rat fibroblasts revealed by an excisable retroviral vector. Cell Growth Differ. 9:1998;381-391.
12. Limon J., Dal Cin P., Sandberg A.A. Application of long-term collagenase disaggregation for the cytogenetic analysis of human solid tumors. Cancer Genet Cytogenet. 23:1986;305-313.
13. Chirgwin J.M., Przybyla A.E., MacDonald R.J., Rutter W.J. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry. 18:1979;5294-5299.
14. Ney P.A., Andrews N.C., Jane S.M., Safer B., Purucker M.E., Weremowicz S., Morton C.C., Goff S.C., Orkin S.H., Nienhuis A.W. Purification of the human NF-E2 complex. cDNA cloning of the hematopoietic cell-specific subunit and evident for an associated partner Mol Cell Biol. 13(9):1993;5604-5612.
15. Vachon G., Cohen B., Pfeifle C., McGuffin M.E., Botas J., Coheb S.M. Homeotic genes of the bithorax complex repress limb development in the abdomen of the Drosophila embryo through the target gene Distalless. Cell. 71:1992;437-450.
16. Osborne L.R., Herbrick J.A., Greavette T., Heng H.H., Tsui L.C., Scherer S.W. PMS2-related genes flank rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7. Genomics. 45:1997;402-406.
17. Yi J., Beckerle M.C. The human TRIP6 gene encodes a LIM domain protein and maps to chromosome 7q22, a region associated with tumorigenesis. Genomics. 49:1998;314-316.
18. Tsui L.-C., Donis-Keller H., Grzeschik K.-H. Report of the second international workshop on human chromosome 7 mapping. 1994. Cytogenet Cell Genet. 71:1995;1-13.
19. Zeng W.R., Scherer S.W., Koutsilieris M., Huizenga J.J., Filteau F., Tsui L.-C., Nepveu A. Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas. Oncogene. 14:1997;2355-2365.
20. Ishiai M., Dean F.B., Okumura K., Abe M., Moon K.Y., Amin A.A., Kagotani K., Taguchi H., Murakami Y., Hanaoka F., O'Donnell M., Hurwitz J., Eki T. Isolation of human and fission yeast homologues of the budding yeast origin recognition complex subunit ORC5. human homologue ORC5L maps to 7q22 Genomics. 46:1997;294-298.