Research Topics
Species | Hannaleena EerolaSummaryCountry: Finland Publications
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Publications
BACH1 Ser919Pro variant and breast cancer riskPia Vahteristo
Department of Obstetrics, Helsinki University Central Hospital, Helsinki, Finland
BMC Cancer 6:19. 2006..In this study, we aimed to evaluate whether there are BACH1 genetic variants that contribute to breast cancer risk in Finland...
Basal cytokeratins in breast tumours among BRCA1, BRCA2 and mutation-negative breast cancer familiesHannaleena Eerola
Department of Oncology, Helsinki University Central Hospital, Haartmaninkatu, 00029 HUS, Helsinki Finland
Breast Cancer Res 10:R17. 2008..Finding new immunohistochemical markers that are specific to hereditary breast cancer could help us to select candidates for BRCA1/BRCA2 mutation testing and to understand the biological pathways of tumour development...
Cyclin D1 expression is associated with poor prognostic features in estrogen receptor positive breast cancerKirsimari Aaltonen
Department of Oncology, Helsinki University Central Hospital, P O Box 180, FI 00029 HUS, Helsinki, Finland
Breast Cancer Res Treat 113:75-82. 2009..0005). In conclusion, the findings of this study show that cyclin D1 has separate roles, and proliferation is driven by different mechanisms in ER positive and negative breast cancers...
Relationship of patients' age to histopathological features of breast tumours in BRCA1 and BRCA2 and mutation-negative breast cancer familiesHannaleena Eerola
Department of Oncology, Helsinki University Central Hospital, Finland
Breast Cancer Res 7:R465-9. 2005..In sporadic breast cancer, tumours from premenopausal patients have been shown to differ from those of postmenopausal patients, but this phenomenon has been little studied among familial patients...
Familial breast cancers without mutations in BRCA1 or BRCA2 have low cyclin E and high cyclin D1 in contrast to cancers in BRCA mutation carriersKirsimari Aaltonen
Department of Oncology, Helsinki University Central Hospital, Helsinki, Finland
Clin Cancer Res 14:1976-83. 2008..Cyclin E expression in tumors of BRCA1 or BRCA2 carriers is higher, and cyclin D1 expression lower, than in sporadic tumors. In familial non-BRCA1/2 tumors, cyclin E and cyclin D1 expression has not been studied...
Histopathological features of breast tumours in BRCA1, BRCA2 and mutation-negative breast cancer familiesHannaleena Eerola
Department of Oncology, Helsinki University Central Hospital, Helsinki, Finland
Breast Cancer Res 7:R93-100. 2005....
Genome-wide association study identifies novel breast cancer susceptibility lociDouglas F Easton
CR UK Genetic Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge CB1 8RN, UK
Nature 447:1087-93. 2007..05 level compared with an estimated 1,343 that would be expected by chance, indicating that many additional common susceptibility alleles may be identifiable by this approach...
Chromosome 5 imbalance mapping in breast tumors from BRCA1 and BRCA2 mutation carriers and sporadic breast tumorsHrefna K Johannsdottir
Department of Pathology, Landspitali-University Hospital, Reykjavik, Iceland
Int J Cancer 119:1052-60. 2006..In conclusion, our results confirm a very high prevalence of chromosome 5q alterations in BRCA1 tumors, pinpointing new regions and genes that should be further investigated...
BARD1 variants Cys557Ser and Val507Met in breast cancer predispositionPia Vahteristo
Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Helsinki, Finland
Eur J Hum Genet 14:167-72. 2006..These results suggest that the contribution of the BARD1 germline variants to breast cancer predisposition is very limited, and that neither Cys557Ser nor Val507Met have an effect on familial breast cancer susceptibility...
Breast cancer patients with p53 Pro72 homozygous genotype have a poorer survivalJohanna Tommiska
Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Finland
Clin Cancer Res 11:5098-103. 2005..The p53 R72P polymorphism has been suggested to play a role in many cancers, including breast cancer. Our aim was to evaluate association of R72P with breast cancer risk as well as histopathologic features of the breast tumors and survival...
No germline FH mutations in familial breast cancer patientsMaija Kiuru
Department of Medical Genetics, Biomedicum Helsinki, University of Helsinki, P.O. Box 63 (Haartmaninkatu 8, FIN-00014 Helsinki, Helsinki, Finland
Eur J Hum Genet 13:506-9. 2005..Most of the cases were selected based on positive family or personal history for malignancies associated with HLRCC. No mutations were found. These results show that FH is not a major predisposing gene for familial breast cancer...
Deletions on chromosome 4 in sporadic and BRCA mutated tumors and association with pathological variablesHrefna K Johannsdottir
Department of Pathology, Landspitali-University Hospital by Hringbraut, Reykjavik, Iceland
Anticancer Res 24:2681-7. 2004..CONCLUSION: The results manifest the frequent alterations of chromosome 4 in BRCA1-associated breast tumors and indicate the location of several genes of potential importance in breast cancer development...
Correlation of CHEK2 protein expression and c.1100delC mutation status with tumor characteristics among unselected breast cancer patientsOuti Kilpivaara
Department of Obstetrics and Gynecology, Helsinki University Central Hospital, FIN 00029 HUS, Finland
Int J Cancer 113:575-80. 2005..02). The c.1100delC germ line mutation also associated strongly with bilateral breast cancer. No significant correlation was seen between CHEK2 status and hormone receptor status, histology, lymph node status, or overall survival...
CHEK2 variant I157T may be associated with increased breast cancer riskOuti Kilpivaara
Department of Obstetrics and Gynecology, Helsinki University Central Hospital HUCH, Helsinki, Finland
Int J Cancer 111:543-7. 2004..The I157T variant may be associated with breast cancer risk, but the risk is lower than for 1100delC...
Genome-wide scanning for linkage in Finnish breast cancer familiesPia Huusko
Cancer Genetics Branch, NHGRI, NIH, Helsinki University, Central Hospital, Helsinki, Finland
Eur J Hum Genet 12:98-104. 2004..Both linkage and association studies are likely to be useful, particularly in other isolated populations...
A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancerPia Vahteristo
Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Haartmaninkatu 8, FIN 00029 HUS, Helsinki, Finland
Am J Hum Genet 71:432-8. 2002....
