Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma. 2011

Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
Klinik für Frauenheilkunde und Geburtshilfe, Universitätsklinikum Jena, Germany. claudia.backsch@med.uni-jena.de

Chromosomal aberrations are a hallmark of human papillomavirus (HPV)-induced cervical carcinogenesis. The aim of this project was to identify structural chromosomal aberrations which may be characteristic for intraepithelial neoplasias (CIN) and cervical carcinomas (CxCa). Two independent HPV16 immortalized keratinocyte cell lines (HPKIA, HPKII) were used as a cell culture model system for cervical carcinogenesis. Different passages of HPKIA and HPKII were analyzed by multicolor spectral karyotyping. Several chromosomal translocations were identified in HPK cells and were validated by interphase fluorescence in situ hybridization (I-FISH). Three unbalanced whole chromosome arm translocations, der(10;14), der(7;21), and der(7;12), were cell line specific. The presence and frequency of these translocations were then examined by I-FISH in frozen tissue sections from normal cervical epithelia (n=6), CIN2/3 (n=15), and CxCa (n=15). The der(10;14) and der(7;21) were detected in 80% and 53.3% of CIN2/3, and in 60% and 46.7% of CxCa, respectively. The percentage of nuclei with translocations in individual lesions was significantly higher among CxCa. The der(7;12) could only be detected in 27% of CIN2/3. None of the translocations were detected in normal cervical epithelia. The translocated chromosomes may contribute to the clonal expansion of subpopulations in these cases and may thus be of diagnostic relevance.

UI MeSH Term Description Entries
D002294 Carcinoma, Squamous Cell A carcinoma derived from stratified SQUAMOUS EPITHELIAL CELLS. It may also occur in sites where glandular or columnar epithelium is normally present. (From Stedman, 25th ed) Carcinoma, Epidermoid,Carcinoma, Planocellular,Carcinoma, Squamous,Squamous Cell Carcinoma,Carcinomas, Epidermoid,Carcinomas, Planocellular,Carcinomas, Squamous,Carcinomas, Squamous Cell,Epidermoid Carcinoma,Epidermoid Carcinomas,Planocellular Carcinoma,Planocellular Carcinomas,Squamous Carcinoma,Squamous Carcinomas,Squamous Cell Carcinomas
D002583 Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. Cancer of Cervix,Cancer of the Cervix,Cancer of the Uterine Cervix,Cervical Cancer,Cervical Neoplasms,Cervix Cancer,Cervix Neoplasms,Neoplasms, Cervical,Neoplasms, Cervix,Uterine Cervical Cancer,Cancer, Cervical,Cancer, Cervix,Cancer, Uterine Cervical,Cervical Cancer, Uterine,Cervical Cancers,Cervical Neoplasm,Cervical Neoplasm, Uterine,Cervix Neoplasm,Neoplasm, Cervix,Neoplasm, Uterine Cervical,Uterine Cervical Cancers,Uterine Cervical Neoplasm
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014178 Translocation, Genetic A type of chromosome aberration characterized by CHROMOSOME BREAKAGE and transfer of the broken-off portion to another location, often to a different chromosome. Chromosomal Translocation,Translocation, Chromosomal,Chromosomal Translocations,Genetic Translocation,Genetic Translocations,Translocations, Chromosomal,Translocations, Genetic
D014407 Tumor Cells, Cultured Cells grown in vitro from neoplastic tissue. If they can be established as a TUMOR CELL LINE, they can be propagated in cell culture indefinitely. Cultured Tumor Cells,Neoplastic Cells, Cultured,Cultured Neoplastic Cells,Cell, Cultured Neoplastic,Cell, Cultured Tumor,Cells, Cultured Neoplastic,Cells, Cultured Tumor,Cultured Neoplastic Cell,Cultured Tumor Cell,Neoplastic Cell, Cultured,Tumor Cell, Cultured
D017404 In Situ Hybridization, Fluorescence A type of IN SITU HYBRIDIZATION in which target sequences are stained with fluorescent dye so their location and size can be determined using fluorescence microscopy. This staining is sufficiently distinct that the hybridization signal can be seen both in metaphase spreads and in interphase nuclei. FISH Technique,Fluorescent in Situ Hybridization,Hybridization in Situ, Fluorescence,FISH Technic,Hybridization in Situ, Fluorescent,In Situ Hybridization, Fluorescent,FISH Technics,FISH Techniques,Technic, FISH,Technics, FISH,Technique, FISH,Techniques, FISH
D045744 Cell Line, Tumor A cell line derived from cultured tumor cells. Tumor Cell Line,Cell Lines, Tumor,Line, Tumor Cell,Lines, Tumor Cell,Tumor Cell Lines
D052162 Human papillomavirus 16 A type of ALPHAPAPILLOMAVIRUS especially associated with malignant tumors of the CERVIX and the RESPIRATORY MUCOSA. HPV 16,HPV16,Human papillomavirus - 16,Human papillomavirus type 16,human papillomavirus type 16 HPV 16,human papillomavirus type 16 HPV16,HPV-16,HPV 16s,HPV16s
D059785 Karyotype The full set of CHROMOSOMES presented as a systematized array of METAPHASE chromosomes from a photomicrograph of a single CELL NUCLEUS arranged in pairs in descending order of size and according to the position of the CENTROMERE. (From Stedman, 25th ed) Karyotypes

Related Publications

Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
January 1988, Journal of medical genetics,
Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
November 2015, International immunopharmacology,
Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
October 2014, Gynecologic oncology,
Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
May 1999, Cancer genetics and cytogenetics,
Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
May 1997, Cancer letters,
Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
February 1993, The British journal of ophthalmology,
Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
May 2005, American journal of medical genetics. Part A,
Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
January 1984, Cytogenetics and cell genetics,
Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
July 1990, Cancer genetics and cytogenetics,
Claudia Backsch, and Birgit Pauly, and Melanie Liesenfeld, and Cornelia Scheungraber, and Mieczyslaw Gajda, and Kristin Mrasek, and Thomas Liehr, and Andreas Clad, and Evelin Schrock, and Ingo B Runnebaum, and Matthias Dürst
June 2010, Cancer genetics and cytogenetics,
Copied contents to your clipboard!