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1.
Br J Cancer ; 107(8): 1423-32, 2012 Oct 09.
Artigo em Inglês | MEDLINE | ID: mdl-22955849

RESUMO

BACKGROUND: Prolyl hydroxylation is a post-translational modification that affects the structure, stability and function of proteins including collagen by catalysing hydroxylation of proline to hydroxyproline through action of collagen prolyl hydroxylases3 (C-P3H) and 4 (C-P4H). Three C-P3Hs (nomenclature was amended according to approval by the HGNC symbols and names at http://www.genenames.org/ and Entrez database at http://www.ncbi.nlm.nih.gov/gene) leucineproline-enriched proteoglycan (leprecan) 1 (Lepre1), leprecan-like 1 (Leprel1), leprecan-like 2 (Leprel2) and two paralogs Cartilage-Related Protein (CRTAP) and leprecan-like 4 (Leprel4) are found in humans. The C-P4Hs are tetrameric proteins comprising a variable α subunit, encoded by the P4HA1, P4HA2 and P4HA3 genes and a constant ß subunit encoded by P4HB. METHODS: We used RT-PCR, qPCR, pyrosequencing, methylation-specific PCR, western blotting and immunohistochemistry to investigate expression and regulation of the C-P3H and C-P4H genes in B lymphomas and normal bone marrow. RESULTS: C-P3H and C-P4H are downregulated in lymphoma. Down-regulation is associated with methylation in the CpG islands and is detected in almost all common types of B-cell lymphoma, but the CpG islands are unmethylated or methylated at lower levels in DNA isolated from normal bone marrow and lymphoblastoid cell lines. Methylation of multiple C-P3H and C-P4H genes is present in some lymphomas, particularly Burkitt's lymphoma. CONCLUSIONS: Methylation of C-P3H and C-P4H is common in B lymphomas and may have utility in differentiating disease subtypes.


Assuntos
Colágeno/genética , Linfoma de Células B/genética , Pró-Colágeno-Prolina Dioxigenase/genética , Linhagem Celular Tumoral , Colágeno/metabolismo , Ilhas de CpG/genética , Regulação da Expressão Gênica , Inativação Gênica , Humanos , Linfoma de Células B/metabolismo , Metilação , Pró-Colágeno-Prolina Dioxigenase/metabolismo
2.
Fetal Diagn Ther ; 23(3): 198-203, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18417978

RESUMO

OBJECTIVES: To investigate if skewed X-chromosome inactivation (XCI) is associated with unexplained recurrent miscarriage (RM) in Greek women. METHODS: This was a prospective case-control study. A methylation-sensitive assay was used to investigate the X-inactivation pattern of women with unexplained RM and controls. RESULTS: Fifty-six of the 74 patients (75.7%) and 55 of 80 controls (68.8%) were informative. Among the informative cases, 6/56 (10.7%) women showed extreme XCI (>90%) and among the informative controls, 2/55 (3.6%) showed extreme XCI. CONCLUSIONS: In the present study, women with unexplained RM showed a statistically nonsignificant increase in skewed XCI prevalence (10.7%) compared with control women (3.6%; p = 0.271).


Assuntos
Aborto Habitual/genética , Inativação do Cromossomo X , Adulto , Estudos de Casos e Controles , Feminino , Grécia , Heterozigoto , Humanos , Masculino , Razão de Chances , Reação em Cadeia da Polimerase , Gravidez , Estudos Prospectivos , Receptores Androgênicos/genética
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