High frequency occurrence of 1-OPRD variant of PRNP gene in gastric cancer cell lines and Chinese population with gastric cancer

Cell Biology International

Volumn 30, Issue 11, 2006, Pages 920-923

  Liang, J ^a   Wang, J B ^a   Pan, Y L ^a   Wang, J ^a   Liu, L L ^a   Guo, X Y ^a   Sun, L ^a   Lin, T ^a   Han, S ^a   Xie, H H ^a   Yin, F ^a   Guo, X G ^a   Fan, D ^a  

^a FOURTH MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

1 OPRD; Gastric cancer; Polymorphism; Prion; PRNP

Indexed keywords

PRION PROTEIN;

1 OCTAPEPTIDE REPEAT DELETION GENE; ADULT; AGED; ARTICLE; CANCER CELL CULTURE; CHINESE; CONTROLLED STUDY; DISEASE COURSE; DNA SEQUENCE; FEMALE; GEL ELECTROPHORESIS; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC VARIABILITY; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; PREVALENCE; STOMACH CANCER;

ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; CELL LINE, TUMOR; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; MALE; MIDDLE AGED; OPEN READING FRAMES; PRIONS; SEQUENCE DELETION; STOMACH NEOPLASMS;

EID: 33750341518     PISSN: 10656995     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cellbi.2006.05.015     Document Type: Article

References (24)

1. Alperovitch A., Zerr I., Pocchiari M., Mitrova E., de Pedro Cuesta J., Hegyi I., et al. Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease. Lancet 353 9165 (1999) 1673-1674
2. Burns C.S., Aronoff-Spencer E., Legname G., Prusiner S.B., Antholine W.E., Gerfen G.J., et al. Copper coordination in the full-length, recombinant prion protein. Biochemistry 42 22 (2003) 6794-6803
3. Castilla J., Gutierrez-Adan A., Brun A., Pintado B., Parra B., Ramirez M.A., et al. Different behavior toward bovine spongiform encephalopathy infection of bovine prion protein transgenic mice with one extra repeat octapeptide insert mutation. J Neurosci 24 9 (2004) 2156-2164
4. Croes E.A., Theuns J., Houwing-Duistermaat J.J., Dermaut B., Sleegers K., Roks G., et al. Octapeptide repeat insertions in the prion protein gene and early onset dementia. J Neurol Neurosurg Psychiatry 75 8 (2004) 1166-1170
5. Du J., Pan Y., Shi Y., Guo C., Jin X., Sun L., et al. Overexpression and significance of prion protein in gastric cancer and multidrug-resistant gastric carcinoma cell line SGC7901/ADR. Int J Cancer 113 2 (2005) 213-220
6. Ellis V., Daniels M., Misra R., and Brown D.R. Plasminogen activation is stimulated by prion protein and regulated in a copper-dependent manner. Biochemistry 41 22 (2002) 6891-6896
7. Erginel-Unaltuna N., Peoc'h K., Komurcu E., Acuner T.T., Issever H., and Laplanche J.L. Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease. Eur J Hum Genet 9 12 (2001) 965-968
8. Georgieva D., Rypniewski W., Echner H., Perbandt M., Koker M., Clos J., et al. Synthetic human prion protein octapeptide repeat binds to the proteinase K active site. Biochem Biophys Res Commun 325 4 (2004) 1406-1411
9. Gonzalez-Iglesias R., Pajares M.A., Ocal C., Espinosa J.C., Oesch B., and Gasset M. Prion protein interaction with glycosaminoglycan occurs with the formation of oligomeric complexes stabilized by Cu(II) bridges. J Mol Biol 319 2 (2002) 527-540
10. Jeong B.H., Nam J.H., Lee Y.J., Lee K.H., Jang M.K., Carp R.I., et al. Polymorphisms of the prion protein gene (PRNP) in a Korean population. J Hum Genet 49 6 (2004) 319-324
11. Lewis V., Collins S., Hill A.F., Boyd A., McLean C.A., Smith M., et al. Novel prion protein insert mutation associated with prolonged neurodegenerative illness. Neurology 60 10 (2003) 1620-1624
12. Liang J., Pan Y., Ning X., Sun L., Lan M., Hong L., et al. Overexpression and related anti-apoptosis function of PrPc in gastric cancer. Tumor Biol 2 27 (2006) 84-91
13. Liang J., Ge F.L., Lu Y.Y., Wang J., Zhai H.H., Yao L.P., et al. Role of PrPc related to apoptosis. EXCLI J 5 (2006) 11-24
14. Palmer M.S., and Collinge J. Mutations and polymorphisms in the prion protein gene. J Hum Mutat 2 3 (1993) 168-173
15. Palmer M.S., Dryden A.J., Hughes J.T., and Collinge J. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature 352 6333 (1991) 340-342
16. Palmer M.S., Mahal S.P., Campbell T.A., Hill A.F., Sidle K.C., Laplanche J.L., et al. Deletions in the prion protein gene are not associated with CJD. Hum Mol Genet 2 5 (1993) 541-544
17. Pan Y, Zhao L, Liang J, Liu J, Shi Y, Liu N, et al. Cellular prion protein promotes invasion and metastasis of gastric cancer. FABES J, in press.
18. Sakudo A., Lee D.C., Nishimura T., Li S., Tsuji S., Nakamura T., et al. Octapeptide repeat region and N-terminal half of hydrophobic region of prion protein (PrP) mediate PrP-dependent activation of superoxide dismutase. Biochem Biophys Res Commun 326 3 (2005) 600-606
19. Salvatore M., Genuardi M., Petraroli R., Masullo C., DAlessandro M., and Pocchiari M. Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease. Hum Genet 94 4 (1994) 375-379
20. Schatzl H.M., Da Costa M., Taylor L., Cohen F.E., and Prusiner S.B. Prion protein gene variation among primates. J Mol Biol 245 4 (1995) 362-374
21. Windl O., Giese A., Schulz-Schaeffer W., Zerr I., Skworc K., Arendt S., et al. Molecular genetics of human prion diseases in Germany. Hum Genet 105 3 (1999) 244-252
22. Yanagihara C., Yasuda M., Maeda K., Miyoshi K., and Nishimura Y. Rapidly progressive dementia syndrome associated with a novel four extra repeat mutation in the prion protein gene. J Neurol Neurosurg Psychiatry 72 6 (2002) 788-791
23. Yu S.L., Jin L., Sy M.S., Mei F.H., Kang S.L., Sun G.H., et al. Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation. Eur J Hum Genet 12 10 (2004) 867-870
24. Zhao Y., You H., Liu F., An H., Shi Y., Yu Q., et al. Differentially expressed gene profiles between multidrug resistant gastric adenocarcinoma cells and their parental cells. Cancer Lett 185 2 (2002) 211-218