Replication error-positive samples found in pheochromocytomas

In Vivo

Volumn 19, Issue 2, 2005, Pages 359-366

  Pecina Slaus, Nives ^a   Nikuseva Martic, Tamara ^a   Gall Troselj, Koraljka ^b   Radic, Kresimir ^a   Hrascan, Reno ^a  

^a UNIVERSITY OF ZAGREB   (Croatia)

^b RUDER BO KOVI INSTITUTE   (Croatia)

Author keywords

APC gene; E cadherin gene; Loss of heterozygosity; Pheochromocytoma; Replication error

Indexed keywords

APC PROTEIN; MYC PROTEIN; UVOMORULIN; WNT PROTEIN;

ADULT; AGED; ALLELE; ARTICLE; CDH 1 GENE; CELL JUNCTION; CONTROLLED STUDY; FEMALE; GENE REPLICATION; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MALE; MICROSATELLITE INSTABILITY; MISMATCH REPAIR; PHEOCHROMOCYTOMA; POLYMERASE CHAIN REACTION; PROTEIN EXPRESSION; TUMOR SUPPRESSOR GENE;

EID: 16344385264     PISSN: 0258851X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (35)

1. Nakao K, Itoh H and Takaya K: Current topics in pheochromocytoma. Biomed Pharmacother 54: 124-128, 2000.
2. Koch CA, Vortmeyer AO, Huang SC, Alesci S, Zhuang Z and Pack K: Genetic aspects of pheochromocytoma. Endocr Regul 35: 43-45, 2001.
3. Dannenberg H, Komminoth P, Dinjens WN, Speel EJ and de Krijger RR: Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas. Endocr Pathol 14: 329-50, 2003.
4. Gimm O, Koch CA, Januszewicz A, Opocher G and Neumann HP: The genetic basis of pheochromocytoma. Front Horm Res 31: 45-60, 2004.
5. Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A et al: Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumor suppressor gene in sporadic and syndromic pheochromocytomas. J Med Genet 32: 934-937, 1995.
6. Friedrich CA: Genotype-phenotype correlation in von Hippel-Lindau syndrome. Hum Mol Genet 10: 763-767, 2001.
7. Neumann HP, Hoegerle S, Manz T, Brenner K and Iliopoulos O: How many pathways to pheochromocytoma. Semin Nephrol 22: 89-99, 2002.
8. Xu W, Mulligan LM, Ponder MA, Liu L, Smith BA, Mathew CG et al: Loss of NF1 alleles in pheochromocytomas from patients with type I neurofibromatosis. Genes Chromosomes Cancer 4: 337-342, 1992.
9. Gutmann DH, Cole JL, Stone WJ, Ponder BA and Collins FS: Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type 1. Genes Chromosomes Cancer 10: 55-58, 1994.
10. Brauch H, Hoeppner W, Jähnig H, Wöhl T, Engelhardt D, Spelsberg F et al: Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret protooncogene. J Clin Endocrinol Metab 82: 4101-4104, 1997.
11. Rubinfeld B, Souza B, Albert I, Muller O, Chamberlain SH, Masiarz FR et al: Association of the APC gene product with β-catenin. Science 262: 1743-1745, 1993.
12. Sieber OM, Tomlison IP and Lamlum H: The adenomatous polyposis coli (APC) tumour suppressor - genetics, function and disease. Mol Med Today 6: 462-469, 2000.
13. Dobashi Y, Katayama K, Kawai M, Akiyama T and Kameya T: APC protein is required for initiation of neuronal differentiation in rat pheochromocytoma PC12 cells. Biochem Biophys Res Commun 279: 685-691, 2000.
14. Peifer M and Polakis P: Wnt signaling in oncogenesis and embriogenesis - a look outside the nucleus. Science 287: 1606-1609, 2000.
15. Kinzler KW and Vogelstein B: Lessons from hereditary colorectal cancer. Cell 87: 159-170, 1996.
16. Groden J, Thliveris A, Samowity W, Carlson M, Gelbert L, Albertsen H et al: Identification and characterization of the familial adenomatous polyposis coli gene. Cell 66: 589-600, 1991.
17. Guilford P: E-cadherin downregulation in cancer: fuel on the fire? Mol Med Today 5: 172-177, 1999.
18. Berx G, Staes K, van Hengel J, Molemans F, Bussemakers MJ, van Bokhoven A et al: Cloning and characterization of the human invasion suppressor gene E-cadherin (CDH1). Genomics 26: 281-289, 1995.
19. Pecina-Slaus N: E-cadherin in normal and tumor cells. Cancer Cell Int E 3: 17-24, 2003.
20. Guilford P, Hopkins J, Harraway J, McLeod M, McLeod N, Harrawira P et al: E-cadherin germline mutations in familial gastric cancer. Nature 392: 402-405, 1998.
21. Barth AI, Nathke IS and Nelson WJ: Cadherins, catenins and APC protein: interplay between cytoskeletal complexes and signaling pathways. Curr Opin Cell Biol 9: 683-690, 1997.
22. Schneider R: The human protooncogene ret: a communicative cadherin? Trends Biochem Sci 17: 468-469, 1992.
23. Iwamoto T, Taniguchi M, Asai N, Ohkusu K, Nakashima I and Takahashi M: cDNA cloning of mouse ret proto-oncogene and its sequence similarity to the cadherin superfamily. Oncogene 8: 1087-1091, 1993.
24. Stockinger A, Eger A, Wolf J, Beug H and Foisner R: E-cadherin regulates cell growth by modulation proliferation-dependent beta-catenin transcriptional activity. J Cell Biol 154: 1185-1196, 2001.
25. Cawkwell L and Quirke P: Direct multiplex amplification of DNA from a formalin fixed, paraffin wax embedded tissue section. Mol Pathol 53: 51-52, 2000.
26. Poljak LJ, Pecina N, DZubur A, Uzarevic B, Vitale B and Pavelic K: Modulation of p62 c-myc expression in a single case of non-T acute lymphoblastic leukemia (ALL) assessed by image analyser. Tumordiagn u. Ther 14: 158-162, 1993.
27. Pecina-Slaus N, Gall-Troselj K, Slaus M, Radic K, Nikuseva-Martic T and Pavelic K: Genetic changes of the E-cadherin and APC tumour suppressor genes in clear cell renal cell carcinoma. Pathology 36: 145-151, 2004.
28. Pecina-Slaus N, Gall-Troselj K, Kapitanovic S, Pavelic J and Pavelic K: Novel alleles of the D16S752 polymorphic genetic marker linked to E-cadherin gene-a potential population marker. Coll Antropol 26: 85-88, 2002.
29. Ionov Y, Peinado MA, Malkhosyan S, Shibata D and Perucho M: Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature 363: 558-561,1993.
30. Aguiar RCT, Cox G, Pomeroy SL and Dahia PLM: Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas. J Clin Endocrinol Metab 86: 2890-2894, 2001.
31. Gumbiner BM: Cell adhesion: The molecular basis of tissue architecture and morphogenesis. Cell 84: 345-357, 1996.
32. Tycko B: Epigenetic gene silencing in cancer. J Clin Invest 105: 401-407, 2000.
33. Cahill DP, Kinzler KW, Vogelstein B and Lengauer C: Genetic instability and darwinian selection in tumours. Trends Cell Biol 9: 57-60, 1999.
34. Dannenberg H, Speel EJ, Zhao J, Saremaslani P, van Der Harst E, Roth J et al: Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas. Am J Pathol 157: 353-359, 2000.
35. Goto K, Ogo A, Yanase T, Haji M, Ohashi M and Nawata H: Expression of c-fos and c-myc proto-oncogenes in human adrenal pheochromocytomas. J Clin Endocrinol Metab 70: 353-357, 1990.