참고문헌
- Barroso E, Pita G, Arias JI, et al (2009). The Fanconi anemia family of genes and its correlation with breast cancer susceptibility and breast cancer features. Breast Cancer Res Treat, 118, 655-60. https://doi.org/10.1007/s10549-009-0439-5
- Betel D, Koppal A, Agius P, Sander C, Leslie C (2010). Comprehensive modeling of microRNA targets predicts functional non-conserved and non-canonical sites. Genome Biol, 11, 8-11. https://doi.org/10.1186/gb-2010-11-s1-p8
- Brewster BL, Rossiello F, French JD, et al (2012). Identification of fifteen novel germline variants in the BRCA1 3'UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target site. Hum Mutat, 33, 1665-75. https://doi.org/10.1002/humu.22159
- Cazzola M, Skoda RC (2000). Translational pathophysiology: a novel molecular mechanism of human disease. Blood, 95, 3280-88.
- Cecener G, Egeli U, Tunca B, et al (2014). BRCA1/2 germline mutations and their clinical importance in Turkish breast cancer patients. Cancer Invest, 1-13.
- Chen Y, Lee W, Chew HK (1999). Emerging roles of BRCA1 in transcriptional regulation and DNA repair. J Cell Physiol, 181, 385-92. https://doi.org/10.1002/(SICI)1097-4652(199912)181:3<385::AID-JCP2>3.0.CO;2-4
- Claus EB, Risch N, Thompson WD (1991). Genetic analysis of breast cancer in the cancer and steroid hormone study. Am J Hum Genet, 48, 232-42.
- Conne B, Stutz A, Vassalli JD (2000). The 3'-untranslated region of messenger RNA: a molecular "hot spot" for pathology? Nat Med, 6, 637-41. https://doi.org/10.1038/76211
- Downs-Holmes C, Silverman P (2011). Breast cancer: overview and updates. The Nurse Practitioner, 36, 20-6.
- Egeli U, Cecener G, Tunca B, Tasdelen I (2006). Novel germline BRCA1 and BRCA2 mutations in Turkish women with breast and/or ovarian cancer and their relatives. Cancer Invest, 24, 484-91. https://doi.org/10.1080/07357900600814706
- Erturk E, Cecener G, Egeli U, et al (2014). Expression status of let-7a and miR-335 among breast tumors in patients with and without germ-line BRCA mutations. Mol and Cell Biochem.
- Esquela-Kerscher A, Slack FJ (2006). Oncomirs-microRNAs with a role in cancer. Nat Rev Cancer, 6, 259-69. https://doi.org/10.1038/nrc1840
- Ferla R, Calo V (2007). Founder mutations in BRCA1 and BRCA2 genes. Ann Oncol, 18, 93-8.
- Ford D, Easton DF, Stratton M, et al (1998). Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. Am J Hum Genet, 62, 676-89. https://doi.org/10.1086/301749
- Goto Y, Yue L, Yokoi A, et al (2001). A novel single-nucleotide polymorphism in the 3'-untranslated region of the human dihydrofolate reductase gene with enhanced expression. Clin Cancer Res, 7, 1952-6.
- Hafez MM, Hassan ZK, Zekri AR, et al (2012). MicroRNAs and metastasis-related gene expression in Egyptian breast cancer patients. Asian Pac J Cancer Prev, 13, 591-8. https://doi.org/10.7314/APJCP.2012.13.2.591
- Hayashita Y, Osada H, Tatematsu Y, et al (2005). A polycistronic microRNA cluster, miR-17-92, is overexpressed in human lung cancers and enhances cell proliferation. Cancer Res, 65, 9628-32. https://doi.org/10.1158/0008-5472.CAN-05-2352
- He L, Thomson JM, Hemann MT, et al (2005). A microRNA polycistron as a potential human oncogene. Nature, 435, 828-33. https://doi.org/10.1038/nature03552
- Hennessy BT, Timms KM, Carey MS, et al (2010). Somatic mutations in BRCA1 and BRCA2 could expand the number of patients that benefit from poly (ADP ribose) polymerase inhibitors in ovarian cancer. J Clin Oncol, 28, 3570-6. https://doi.org/10.1200/JCO.2009.27.2997
- Jemal A, Bray F, Center MM, et al (2011). Global cancer statistics. CA Cancer J Clin, 61, 69-90. https://doi.org/10.3322/caac.20107
- Joseph S, Sellappa S, Prathyumnan S, Keyan KS (2011). A novel polymorphism in BRCA2 exon 8 and breast cancer risk in South India. Asian Pac J Cancer Prev, 12, 309-11.
- Jovanovic M, Hengartner MO (2006). miRNAs and apoptosis: RNAs to die for. Oncogene, 25, 6176-87. https://doi.org/10.1038/sj.onc.1209912
- Kayani Mu, Kayani MA, Malik FA, Faryal R (2011). Role of miRNAs in breast cancer. Asian Pac J Cancer Prev, 12, 3175-80.
- Keen JC, Davidson NE (2003). The biology of breast carcinoma. Cancer, 97, 825-33. https://doi.org/10.1002/cncr.11126
- Kenemans P, Verstraeten RA, Verheijen RH (2004). Oncogenic pathways in hereditary and sporadic breast cancer. Maturitas, 49, 34-43. https://doi.org/10.1016/j.maturitas.2004.06.005
- Khana KK, Jackson SP (2001). DNA double-strand breaks: signaling, repair and the cancer connection. Nat Genet, 27, 247-54. https://doi.org/10.1038/85798
- Kontorovich T, Levy A, Korostishevsky M, Nir U, Friedman E (2010). Single nucleotide polymorphisms in miRNA binding sites and miRNA genes as breast/ovarian cancer risk modifiers in Jewish high-risk women. Int J Cancer, 127, 589-97. https://doi.org/10.1002/ijc.25065
- Kooshyar MM, Nassiri M, Mahdavi M, Doosti M, Parizadeh A (2013). Identification of germline BRCA1 mutations among breast cancer families in Northeastern Iran. Asian Pac J Cancer Prev, 14, 4339-45. https://doi.org/10.7314/APJCP.2013.14.7.4339
- Li JY, Jia S, Zhang WH, et al (2013). Differential distribution of microRNAs in breast cancer grouped by clinicopathological subtypes. Asian Pac J Cancer Prev, 14, 3197-203. https://doi.org/10.7314/APJCP.2013.14.5.3197
- Lu J, Getz G, Miska EA, et al (2005). MicroRNA expression profiles classify human cancers. Nature, 435, 834-8. https://doi.org/10.1038/nature03702
- Miki Y, Swensen J, Shattuck-Eidens D, et al (1994). A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science, 266, 66-71. https://doi.org/10.1126/science.7545954
- Nicoloso MS, Sun H, Spizzo R, et al (2010). Single-nucleotide polymorphisms inside microRNA target sites influence tumor susceptibility. Cancer Res, 70, 2789-98. https://doi.org/10.1158/0008-5472.CAN-09-3541
- Nilsen TW (2007). Mechanisms of microRNA-mediated gene regulation in animal cells. Trends Genet, 23, 243-9. https://doi.org/10.1016/j.tig.2007.02.011
- O'Donnell KA, Wentzel EA, Zeller KI, Dang CV, Mendell JT (2005). c-MYC regulated microRNAs modulate E2F-1 expression. Nature, 435, 839-43. https://doi.org/10.1038/nature03677
- Pelletier C, Speed WC, Paranjape T, et al (2011). Rare BRCA1 haplotypes including 3'UTR SNPs associated with breast cancer risk. Cell Cycle, 10, 90-9. https://doi.org/10.4161/cc.10.1.14359
- Peto I, Collins N, Barfoot R, et al (1999). Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer. J Natl Cancer Inst, 91, 943-9. https://doi.org/10.1093/jnci/91.11.943
- Pongsavee M, Yamkamon V, Dakeng S, et al (2009). The BRCA1 3'-UTR: 5711?421T/T_5711?1286T/T genotype is a possible breast and ovarian cancer risk factor. Genet Test Mol Biomarkers, 13, 307-17. https://doi.org/10.1089/gtmb.2008.0127
- Scully R, Livingston DM (2000). In search of the tumoursuppressor functions of BRCA1 and BRCA2. Nature, 408, 429-32. https://doi.org/10.1038/35044000
- Sehl ME, Langer LR, Papp JC, et al (2009). Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer. Clin Cancer Res, 15, 2192-203. https://doi.org/10.1158/1078-0432.CCR-08-1417
- Szabo CI, King MC (1997). Population genetics of BRCA1 and BRCA2. Am J Hum Genet, 60, 1013-20.
- Wooster R, Bignell G, Lancaster J, et al (1995). Identification of the breast cancer susceptibility gene BRCA2. Nature, 378, 789-92. https://doi.org/10.1038/378789a0
- Wu W, Sun M, Zou GM, Chen J (2007). MicroRNA and cancer: current status and prospective. Int J Cancer, 120, 953-60.
- Venkitaraman AR (2002). Cancer susceptibility and the functions of BRCA1and BRCA2. Cell, 108, 171-82. https://doi.org/10.1016/S0092-8674(02)00615-3
- Zhang B, Pan X, Anderson TA (2006). MicroRNA: a new player in stem cells. J Cell Physiol, 209, 266-9. https://doi.org/10.1002/jcp.20713
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