PCC and COBRA-FISH a new tool to characterize primary cervical carcinomas: To assess hall-marks and stage specificity

Cancer Letters

Volumn 287, Issue 1, 2010, Pages 67-74

  Darroudi, Firouz ^a   Bergs, Judith W J ^b   Bezrookove, Vladimir ^a   Buist, Marrije R ^b   Stalpers, Lukas J ^b   Franken, Nicolaas A P ^b  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

Chemically induced PCC; Chromosomal abnormalities; COBRA FISH; Primary cervical cancer; Stage specificity

Indexed keywords

ARTICLE; CANCER GROWTH; CANCER STAGING; CHROMOSOME LOSS; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC GAIN; HUMAN; HUMAN TISSUE; KARYOTYPE; METAPHASE; NUMERICAL CHROMOSOME ABERRATION; PREMATURE CHROMOSOME CONDENSATION; PRIORITY JOURNAL; STRUCTURAL CHROMOSOME ABERRATION; TETRAPLOIDY; TRIPLOIDY; UTERINE CERVIX BIOPSY; UTERINE CERVIX CARCINOMA;

ADENOCARCINOMA; CARCINOMA, SQUAMOUS CELL; CELL LINE, TUMOR; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; NEOPLASM STAGING; UTERINE CERVICAL NEOPLASMS;

EID: 72049102604     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.canlet.2009.05.034     Document Type: Article

References (35)

1. Mitelman F. Recurrent chromosome aberrations in cancer. Mutat. Res. 462 (2000) 247-253
2. Hagmar L., Stromberg U., Tinnerberg H., and Mikoczy Z. The usefulness of cytogenetic biomarkers as intermediate endpoints in carcinogenesis. Int. J. Hyg. Environ. Health 204 (2001) 43-47
3. Tallini G., Dorfman H., Brys P., Dal Cin P., De W.I., Fletcher C.D., Jonson K., Mandahl N., Mertens F., Mitelman F., Rosai J., Rydholm A., Samson I., Sciot R., Van den B.H., Vanni R., and Willen H. Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the chromosomes and morphology (CHAMP) collaborative study group. J. Pathol. 196 (2002) 194-203
4. Boffetta P., van der Hel O., Norppa H., Fabianova E., Fucic A., Gundy S., Lazutka J., Cebulska-Wasilewska A., Puskailerova D., Znaor A., Kelecsenyi Z., Kurtinaitis J., Rachtan J., Forni A., Vermeulen R., and Bonassi S. Chromosomal aberrations and cancer risk: results of a cohort study from Central Europe. Am. J. Epidemiol. 165 (2007) 36-43
5. Mitelman F., Johansson B., Mandahl N., and Mertens F. Clinical significance of cytogenetic findings in solid tumors. Cancer Genet. Cytogenet. 95 (1997) 1-8
6. Ried T., Liyanage M., du Manoir S., Heselmeyer K., Auer G., Macville M., and Schrock E. Tumor cytogenetics revisited: comparative genomic hybridization and spectral karyotyping. J. Mol. Med. 75 (1997) 801-814
7. Pinkel D., Segraves R., Sudar D., Clark S., Poole I., Kowbel D., Collins C., Kuo W.L., Chen C., Zhai Y., Dairkee S.H., Ljung B.M., Gray J.W., and Albertson D.G. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat. Genet. 20 (1998) 207-211
8. Koopman L.A., Szuhai K., van Eendenburg J.D., Bezrookove V., Kenter G.G., Schuuring E., Tanke H., and Fleuren G.J. Recurrent integration of human papillomaviruses 16, 45, and 67 near translocation breakpoints in new cervical cancer cell lines. Cancer Res. 59 (1999) 5615-5624
9. Fujimoto T., Nishikawa A., Iwasaki M., Akutagawa N., Teramoto M., and Kudo R. Gene expression profiling in two morphologically different uterine cervical carcinoma cell lines derived from a single donor using a human cancer cDNA array. Gynecol. Oncol. 93 (2004) 446-453
10. Heselmeyer K., Schrock E., du Manoir S., Blegen H., Shah K., Steinbeck R., Auer G., and Ried T. Gain of chromosome 3q defines the transition from severe dysplasia to invasive carcinoma of the uterine cervix. Proc. Natl. Acad. Sci. (USA) 93 (1996) 479-484
11. Heselmeyer K., Macville M., Schröck E., Blegen H., Hellström A.C., Shah K., Auer G., and Ried T. Advanced-stage cervical carcinomas are defined by a recurrent pattern of chromosomal aberrations revealing high genetic instability and a consistent gain of chromosome arm 3q. Genes, Chromosomes Cancer 19 (1997) 233-240
12. Harris C.P., Lu X.Y., Narayan G., Singh B., Murty V.V.V.S., and Rao P.H. Comprehensive molecular cytogenetic characterization of cervical cancer cell lines. Genes Chromosomes Cancer 36 (2003) 233-241
13. Gotoh E., Asakawa Y., and Kosaka H. Inhibition of protein serine threonine phosphatases directly induces premature chromosome condensation in mammalian somatic cells. Biomed. Res. 16 (1995) 63-68
14. Kanda R., Eguchi-Kasai K., and Hayata I. Phosphatase inhibitors and premature chromosome condensation in human peripheral lymphocytes at different cell-cycle phases. Somat. Cell Genet. 25 (1999) 1-8
15. Prasanna P.G., Escalada N.D., and Blakely W.F. Induction of premature chromosome condensation by a phosphatase inhibitor and a protein kinase in unstimulated human peripheral blood lymphocytes: a simple and rapid technique to study chromosome aberrations using specific whole-chromosome DNA hybridization probes for biological dosimetry. Mutat. Res. 466 (2000) 131-141
16. Steinmann K.E., Belinsky G.S., Lee D., and Schlegel R. Chemically induced premature mitosis: differential response in rodent and human cells and the relationship to cyclin B synthesis and p34cdc2/cyclin B complex formation. Proc. Natl. Acad. Sci. (USA) 88 (1991) 6843-6847
17. van Oosten M., Stout G.J., Backendorf C., Rebel H., de Wind N., Darroudi F., van Kranen H.J., de Gruijl F.R., and Mullenders L.H. Mismatch repair protein Msh2 contributes to UVB-induced cell cycle arrest in epidermal and cultured mouse keratinocytes. DNA Repair (Amsterdam) 4 (2005) 81-89
18. Coco-Martin J.M., and Begg A.C. Detection of radiation-induced chromosome aberrations using fluorescence in situ hybridization in drug-induced premature chromosome condensations of tumour cell lines with different radiosensitivities. Int. J. Radiat. Biol. 71 (1997) 265-273
19. Bergs J.W., Franken N.A., ten Cate R., van Bree C., and Haveman J. Effects of cisplatin and gamma-irradiation on cell survival, the induction of chromosomal aberrations and apoptosis in SW-1573 cells. Mutat. Res. 594 (2006) 148-154
20. Darroudi F., Bezrookove V., Fomina J., Mesker W.E., Wiegant J.C., Raap A.K., and Tanke H.J. Insights into the sites of X ray and neutron induced chromosomal aberrations in human lymphocytes using COBRA-MFISH. Radiat. Prot. Dosim. 99 (2002) 189-192
21. Bezrookove V., Smits R., Moeslein G., Fodde R., Tanke H.J., Raap A.K., and Darroudi F. Premature chromosome condensation revisited: a novel chemical approach permits efficient cytogenetic analysis of cancers. Genes Chromosomes Cancer 38 (2003) 177-186
22. Wiegant J., Bezrookove V., Rosenberg C., Tanke H.J., Raap A.K., Zhang H., Bittner M., Trent J.M., and Meltzer P. Differentially painting human chromosome arms with combined binary ratio-labeling fluorescence in situ hybridization. Genome. Res. 10 (2000) 861-865
23. Wittekind C., Compton C.C., Greene F.L., and Sobin L.H. TNM residual tumor classification revisited. Cancer 94 (2002) 2511-2516
24. Horn L.C., Fischer U., Raptis G., Bilek K., and Hentschel B. Tumor size is of prognostic value in surgically treated FIGO stage II cervical cancer. Gynecol. Oncol. 107 (2007) 310-315
25. Tanke H.J., Wiegant J., van Gijlswijk R.P., Bezrookove V., Pattenier H., Heetebrij R.J., Talman E.G., Raap A.K., and Vrolijk J. New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling. Eur. J. Hum. Genet. 7 (1999) 2-11
26. Ronco G., Segnan N., Giorgi-Rossi P., Zappa M., Casadei G.P., Carozzi F., Dalla Palma P., Del Mistro A., Folicaldi S., Gillio-Tos A., Nardo G., Naldoni C., Schincaglia P., Zorzi M., Confortini M., and Cuzick J. New Technologies for Cervical Cancer Working Group. Human papillomavirus testing and liquid-based cytology: results at recruitment from the new technologies for cervical cancer randomized controlled trial. J. Nat. Cancer Inst. 98 (2006) 765-774
27. Duensing S., and Munger K. Centromsome abnormalities, genomic instability and carcinogenic progression. Biochem. Biophys. Acta 1471 (2001) M81-M88
28. Melsheimer P., Vinokurova S., Wentzensen N., Bastert G., and von Knebel Doeberitz M. DNA aneuploidy and integration of human papillomavirus type 16 e6/e7 oncogenes in intraepithelial neoplasia and invasive squamous cell carcinoma of the cervix uteri. Clin. Cancer Res. 10 (2004) 3059-3063
29. Bollmann G., Mehes R., Torka R., Spiech N., Schmitt C., and Bollmann M. Determination of features indicating progression in atypical squamous cells with undetermined significance: human papillomavirus typing and DNA ploidy analysis from liquid-based cytologic samples. Cancer 93 (2003) 113-117
30. Atkin N.B., and Baker M.C. Nonrandom chromosome chnages in carcinoma of cervix uteri. I. Nine near-diploid tumors. Cancer Genet. Cytogenet. 7 (1982) 209-222
31. Brink A.A.T.P., Wiegant J.C.A.G., Szuhai K., Tanke H.J., Kenter G.G., Fleuren G.J., Schuuring E., and Raap A.K. Simultaneous mapping of human papillomavirus integration sites and molecular karyotyping in short-term cultures of cervical carcinomas by using 49-color combined binary ratio labelling fluorescence in situ hybridization. Cancer Genet. Cytogenet. 134 (2004) 145-150
32. Kirchhoff M., Rose H., Peterson B.L., Maahr J., Gerder T., Lundsteen C., Bryndorf T., Kryger-Baggesen N., Christensen L., Engelholm S.A., and Philip J. Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma. Genes Chromosomes Cancer 24 (1999) 144-150
33. Kloth J.N., Oosting J., van Wezel T., Szuhai K., Knijnenburg J., Gorter A., Kenter G.G., Fleuren G.J., and Jordanova E.S. Combined array-comparative hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer. BMC Genom. 8 (2007) 1-13
34. Hidalgo A., Monroy A., Arana R.M., Taja L., Vazquez G., and Salcedo M. Chromosomal imbalances in four new uterine cervix carcinoma derived cell lines. BMC Cancer 3 (2003) 1-5
35. Knutsen T., Gobu V., Knaus R., Padilla-Nash H., Auhustus M., Strausberg R.L., Kirsch I.R., Sirotkin K., and Ried T. The interactive online SKY/M-FISH & CGH database and the entrez cancer chromosome search database: Linkage of chromosome aberrations with the genome sequence. Genes Chromosomes Cancer 44 (2005) 52-64