Genetic factors in etiology of uterine fibroids;Genetické faktory v etiopatogenezi děložních myomu

Ceska Gynekologie

Volumn 77, Issue 1, 2012, Pages 58-60

  Kubínová, Kristýna ^a   Mara M ^a   Horak P ^a   Kuzel D ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

Author keywords

Chromosomal aberration; Cytogenetic; Uterine fibroid

Indexed keywords

FUMARATE HYDRATASE;

ARTICLE; CHROMOSOME ABERRATION; FEMALE; GENE TRANSLOCATION; GENETICS; HUMAN; LEIOMYOMA; MUTATION;

CHROMOSOME ABERRATIONS; FEMALE; FUMARATE HYDRATASE; HUMANS; LEIOMYOMA; MUTATION; TRANSLOCATION, GENETIC;

EID: 84858761479     PISSN: 12107832     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (23)

1. Barker, KT., Spendlove, HE., Banu, NS., et al. No evidence for epigenetic inactivation of fumarate hydratase in leiomyomas and leiomyosarcomas. Cancer Letters, 2006, 235, 1, p. 136-140.
2. Cramer, SF. The frequency of uterine leiomyomas. Amer J Clin Pathol, 1990, 94, p. 435-438. (Pubitemid 20316570)
3. Goedken, J., Rock JA. Uterine fibroids: Epidemiology and overview. In Tulandi, T. Uterine fibroids: Embolization and other treatments. Cambridge: Cambridge University press. 2003. 147 p.
4. Hennig, Y., Deichert, U., Bonk, U., et al. Chromosomal translocations affecting 12q14-15 but not deletions of the long arm of chromosome 7 associated with a growth advantage of uterine smooth muscle cells. Molecular Hum Reprod, 1999, 5, p. 1150-1154.
5. Hodge, J., Morton, CC. Genetic heterogeneity among uterine leiomyomata: insights into malignant progression. Hum Molecular Genet, 2007, 16, p. R7-13.
6. Hodge, J., Park, PJ., Dreyfuss, JM., et al. Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis. Genes, Chromosomes & Cancer. 2009, 48, 10, p. 865-885.
7. Holub, Z., et al. Management dìložních myomù: CSGE doporuèení k provádìní správná klinická praxe. Èes Gynek, 2005, 70, s. 165-167.
8. Kiuru, M., Lehtonen, R., Arola, J., et. al. Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families. Cancer Res, 2002, 62, p. 16.
9. Kubínová, K. Perspektivy radiologická láèby myomù. In Mára, M. Dìlož ní myomy: Moderní diagnostika a láèba. Praha: Grada Publishing. 2009. 231 s.
10. Launonen, V., Vierimaa, O., Kuiru, M., et al. Inherited susceptibility to uterine leiomyomas and renal cell cancer. Proceedings of the National Academy of Sciences of the United States of America. 2001, 98, s. 3387-92 (Pubitemid 32220855)
11. Lehtonen, R., Kiuru, M., Vanharanta, S., et al. Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors. Amer J Pathol, 2004, 164, p. 17-22. (Pubitemid 38364585)
12. Ligon, AH., Morton, CC. Leiomyomata: heritability and cytogenetic studies. Hum Reprod Update, 2001, 7, p. 8-14. (Pubitemid 32111961)
13. Mára, M. Indikace k embolizaci myomù. In MÁRA, M. Dìložní myomy: moderní diagnostika a láèba. Praha: Grada Publishing. 231 s.
14. Mark, J., Havel, G., Grepp, C., et al. Chromosomal patterns in human benign uterine leiomyomas. Cancer Genet Cytogenet, 1990, 44, 1, p. 1-13. (Pubitemid 20039178)
15. Meloni, AM., Surti, U., Contento, AM., et al. Uterine leiomyomas: cytogenetic and histologic profile. Obstet Gynec, 1992, 80, p. 209-217.
16. Okolo, S. Incidence, aetiology and epidemiology of uterine fibroids. BailliŹre, 2008, 22, 4, p. 571-588. (Pubitemid 351804127)
17. Ozisik, YY., Meloni, AM., Stephenson, CF., et al. Chromosome abnormalities in breast fibroadenomas. Cancer Genet Cytogenet, 1994, 77, 2, p. 125-128. (Pubitemid 24346075)
18. Ozisik, YY., Meloni, AM., Altungoz, O., et al. Translocation (6;10)(p21;q22) in uterine leiomyomas. Cancer Genet Cytogenet, 1995, 79, 2, p. 136-138.
19. Parker, W. Etiology, symptomatology, and diagnosis of uterine myomas. Fertil Steril, 2007, 87, p. 725-736. (Pubitemid 46553757)
20. Reeves, R. Molecular biology of HMGA proteins: hubs of nuclear function. Gene, 2001, 277, p. 63-81. (Pubitemid 32972109)
21. Rein, MS., Powell, WL., Walters, FC., et al. Cytogenetic abnormalities in uterine myomas are associated with myoma size. Molecular Hum Reprod, 1998, 4, 1, p. 83-86. (Pubitemid 28109165)
22. Tomlinson, IP., Alam, NA., Rowan, AJ., et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. Nature Genet, 2002, 30, p. 406-410.
23. Xing, YP., Powell, WL., Morton, CC. The del(7q) subgroup in uterine leiomyomata : genetic and biologic characteristics. Further evidence for the secondary nature of cytogenetic abnormalities in the pathobiology of uterine leiomyomata. Cancer Genet Cytogenet, 1997, 98, p. 69-74.