참고문헌
- Antoniou AC, Wang X, Fredericksen ZS, et al (2010). A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. Nat Genet, 42, 885-92. https://doi.org/10.1038/ng.669
- Ahmed S, Thomas G, Ghoussaini M, et al (2009). Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat Genet, 41, 585-90. https://doi.org/10.1038/ng.354
- Balmain A, Gray J, Ponder B (2003). The genetics and genomics of cancer. Nat Genet, 33, 238-44. https://doi.org/10.1038/ng1107
- Crown Human Genome Center, Department of Molecular Genetics, the Weizmann Institute of Science. 2014. Catenin (cadherin-associated protein), alpha 2. Accessed August 2, 2014, at http://www.genecards.org/cgi-bin/carddisp.pl?gene=CTNNA2.
- Crown Human Genome Center, Department of Molecular Genetics, the Weizmann Institute of Science. 2014. Testis expressed 10. Accessed August 2, 2014, at http://www.genecards.org/cgi-bin/carddisp.pl?gene=TEX10.
- Easton DF, Pooley KA, Dunning AM, et al (2007). Genome-wide association study identifies novel breast cancer susceptibility loci. Nature, 447, 1087-93. https://doi.org/10.1038/nature05887
- Fanjul-Fernandez M, Quesada V, Cabanillas R, et al (2013). Cell-cell adhesion genes CTNNA2 and CTNNA3 are tumor suppressors frequently mutated in laryngeal carcinomas. Nat Commun, 4, 2351.
- Fletcher O, Johnson N, Orr N, et al (2011). Novel breast cancer susceptibility locis at 9q31.2: results of a genome-wide association study. J Natl Cancer Inst, 103, 425-35. https://doi.org/10.1093/jnci/djq563
- Gaudet MM, Kirchhoff T, Green T, et al (2010). Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. PLoS Gene, 6, 1001183. https://doi.org/10.1371/journal.pgen.1001183
- Gold B, Kirchhoff T, Stefanov S, et al (2008). Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.23. Proc Natl Acad Sci USA, 105, 4340-5. https://doi.org/10.1073/pnas.0800441105
- Guan YP, Yang XX, Yao GY, et al (2014). Breast cancer association studies in a Han Chinese population using 10 European-ancestry-associated breast cancer susceptibility SNPs. Asian Pac J Cancer Prev, 15, 85-91. https://doi.org/10.7314/APJCP.2014.15.1.85
- Hunter DJ, Kraft P, Jacobs KB, et al (2007). A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet, 39, 870-4. https://doi.org/10.1038/ng2075
- Iodice S, Barile M, Rotmensz N, et al (2010). Oral contraceptive use and breast or ovarian cancer risk in BRCA1/2 carriers: a meta-analysis. Eur J Cancer, 46, 2275-84. https://doi.org/10.1016/j.ejca.2010.04.018
- Islam T, Ito H, Sueta A, et al (2013). Alcohol and dietary folate intake and the risk of breast cancer: a case-control study in Japan. Eur J Cancer Prev, 22, 358-66. https://doi.org/10.1097/CEJ.0b013e32835b6a60
- Kim HC, Lee JY, Sung H, et al (2012). A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Strudy. Breast Cancer Research, 14, 56.
- Liang H, Samanta S, Nagarajan L (2005). SSBP2, a candidate tumor suppressor genem induces growth arrest and differentiation of myeloid leukemia cells. Oncogene, 24, 2625-34. https://doi.org/10.1038/sj.onc.1208167
- Long J, Cai Q, Shu XO, et al (2010). Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the asia breast cancer consortium. PLoS Genet, 6, 1001002. https://doi.org/10.1371/journal.pgen.1001002
- Mahdi KM, Nassiri MR, Nasiri K (2013). Hereditary genes and SNPs associated with breast cancer. Asian Pac J Cancer Prev, 14, 3403-9. https://doi.org/10.7314/APJCP.2013.14.6.3403
- Nathanson KL, Wosster R, Weber BL (2001). Breast cancer genetics: what we know and what we need. Nat Med, 7, 552-6. https://doi.org/10.1038/87876
- Ng CH, Pathy NB, Taib NA, et al (2011). Comparison of breast cancer in Indonesia and Malaysia . a clinico-pathological study between Dharmais Cancer Centre Jakarta and University Malaya Medical Centre, Kuala Lumpur. Asian Pacific J Cancer Prev, 12, 2943-6.
- Phipps AI, Chlebowski RT, Prentice R, et al (2011). Reproductive history and oral contraceptive use in relation to risk of triple-negative breast cancer. J Natl Cancer Inst, 103, 1-8. https://doi.org/10.1093/jnci/djq540
- Stacey SN, Manolescu A, Sulem P, et al (2007). Common variants on chromosome 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet, 39, 865-9. https://doi.org/10.1038/ng2064
- Stacey SN, Manolescu A, Sulem P, et al (2008). Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet, 40, 703-6. https://doi.org/10.1038/ng.131
- Shu XO, Long J, Lu W, et al (2012). Novel genetic markers of breast cancer survival identified by a genome-wide association study. Cancer Res, 72, 1182-9. https://doi.org/10.1158/0008-5472.CAN-11-2561
- The National Center for Biotechnology Information. 2014. CTNNA2 catenin (cadherin-associated protein), alpha 2. Accessed August 2, 2014, at http://www.ncbi.nlm.nih.gov/gene/1496.
- The National Center for Biotechnology Information. 2014. MTCL1 microtubule crosslinking factor 1. Accessed August 2, 2014, at http://www.ncbi.nlm.nih.gov/gene/23255.
- The National Center for Biotechnology Information. 2014. SSBP2 single-stranded DNA binding protein 2. Accessed August 2, 2014, at http://www.ncbi.nlm.nih.gov/gene/23635.
- The National Center for Biotechnology Information. 2014. TEX10 testis expressed 10. Accessed August 2, 2014, at http://www.ncbi.nlm.nih.gov/gene/54881.
- Thomas G, Jacobs KB, Kraft P, et al (2009). A multi-stage genome-wide association in breast cancer identifies two novel risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Nat Genet, 41, 579-84. https://doi.org/10.1038/ng.353
- Tjindarbumi D, Mangunkusumo R (2002). Cancer in Indonesia, present and future. Jpn J Clin Oncol, 32, 17-21. https://doi.org/10.1093/jjco/hye123
- Turnbull C, Ahmed S, Morrison J, et al (2010). Genome-wide association study identifies five new breast cancer susceptibility loci. Nat Genet, 42, 504-7. https://doi.org/10.1038/ng.586
- Xiao Y, Decker PA, Rice T, et al (2012). SSBP2 variants are associated with survival in glioblastoma patients. Clin Cancer Res, 18, 3154-62. https://doi.org/10.1158/1078-0432.CCR-11-2778
- Yoshitake H, Yokoi H, Ishikawa H, et al (2012). Overexpression of TEX10, a potential novel cancer marker, in head and neck squamous cell carcinoma. Cancer Biomark, 12, 141-8.
- Zhang B, Beeghly-fadiel A, Long J, et al (2011). Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence. Lancet Oncol, 12, 477-88. https://doi.org/10.1016/S1470-2045(11)70076-6
- Zheng W, Long J, Gao YT, et al (2009). Genome-wide association study identifies a novel breast cancer susceptibility locus at 6q25.1. Nat Genet, 41, 324-8. https://doi.org/10.1038/ng.318
- Zheng W, Cai Q, Signorello LB, et al (2009). Evaluation of 11 breast cancer susceptibility loci in African-American women. Cancer Epidemiol Biomarkers Prev, 18, 2761-4. https://doi.org/10.1158/1055-9965.EPI-09-0624
- Zheng W, Wen W, Gao YT, et al (2010). Genetic and clinical predictors for breast cancer risk assessment and stratification among Chinese women. J Natl Cancer Inst, 102, 972-81. https://doi.org/10.1093/jnci/djq170
피인용 문헌
- BRCA1 Gene Mutation Screening for the Hereditary Breast and/or Ovarian Cancer Syndrome in Breast Cancer Cases: a First High Resolution DNA Melting Analysis in Indonesia vol.17, pp.3, 2016, https://doi.org/10.7314/APJCP.2016.17.3.1539
- Improving the detection of pathways in genome-wide association studies by combined effects of SNPs from Linkage Disequilibrium blocks vol.7, pp.1, 2017, https://doi.org/10.1038/s41598-017-03826-2