Research Topics
Genomes and GenesSpecies | H GronbergSummaryCountry: Sweden Publications
| Collaborators
|
Detail Information
Publications
BRCA2 mutation in a family with hereditary prostate cancerH Gronberg
Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden
Genes Chromosomes Cancer 30:299-301. 2001..Although BRCA2 is probably responsible only for a very small fraction of hereditary prostate cancers, this finding supports previous reports of an increased risk of prostate cancer in BRCA2 mutation carriers...
Prostate cancer epidemiologyHenrik Gronberg
Department of Radiation Sciences Oncology, Umea University, 901 85, Umea, Sweden
Lancet 361:859-64. 2003..Several important issues could help in our understanding of this disease-the variation in incidence of prostate cancer between ethnic populations and the factors leading to familial clustering of the diseases...
In Swedish families with hereditary prostate cancer, linkage to the HPC1 locus on chromosome 1q24-25 is restricted to families with early-onset prostate cancerH Gronberg
Department of Oncology, Umea University, 901 85 Umea, Sweden
Am J Hum Genet 65:134-40. 1999..These results are consistent with the hypothesis of linkage to HPC1 in a subset of families with prostate cancer, particularly those with an early age at diagnosis...
Cancer risk in families with hereditary prostate carcinomaH Gronberg
Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden
Cancer 89:1315-21. 2000..The aim of this study was to investigate whether tumors other than prostate carcinoma aggregate in families with HPC or whether this disease can be considered site specific...
Genetic variation in the COX-2 gene and the association with prostate cancer riskK Shahedi
Department of Radiation Sciences, Oncology, University of Umea, Umea Sweden
Int J Cancer 119:668-72. 2006..036, global simulated p-value=0.046). This study supports the hypothesis that inflammation is involved in prostate carcinogenesis and that sequence variation within the COX-2 gene influence the risk of prostate cancer...
A population based cohort study of patients with multiple colon and endometrial cancer: correlation of microsatellite instability (MSI) status, age at diagnosis and cancer riskK Cederquist
Unit of Medical Genetics, Department of Medical Biosciences, Umea University, S 901 87, Umea, Sweden
Int J Cancer 91:486-91. 2001..Mutations in mismatch repair genes can explain some of the increased risk in these families, but mutations in MSI negative families are probably due to other colon cancer susceptibility genes not yet described...
Microsatellite instability, PTEN and p53 germline mutations in glioma familiesB Malmer
Department of Radiation Science, Oncology, Umea University Hospital, Sweden
Acta Oncol 40:633-7. 2001..Apparently, mutation in the tested tumour suppressor genes or DNA mismatch repair genes does not explain the familial glioma observed in these families...
No link between viral findings in the prostate and subsequent cancer developmentJ Bergh
Department of Medical Biosciences Pathology, Umea University, Umeå S 90185, Sweden
Br J Cancer 96:137-9. 2007....
Comprehensive evaluation of genetic variation in the IGF1 gene and risk of prostate cancerMattias Johansson
Department of Surgical and Perioperative Sciences, Urology and Andrology, Umea University Hospital, Umea, Sweden
Int J Cancer 120:539-42. 2007..Further studies on genetic variations in the IGF1 gene in relation to prostate cancer risk as well as to circulating levels of IGF1 are needed to confirm this novel finding...
Primary brain tumours as second primary: a novel association between meningioma and colorectal cancerB Malmer
Department of Oncology, Umea University, Umea, Sweden
Int J Cancer 85:78-81. 2000..A novel association between meningioma and colorectal cancer, particularly in females, was observed, which justifies further studies to evaluate common aetiological factors...
-160C/A polymorphism in the E-cadherin gene promoter and risk of hereditary, familial and sporadic prostate cancerBjörn Anders Jonsson
Department of Medical Biosciences, Pathology, Umea University, Umea, Sweden
Int J Cancer 109:348-52. 2004..6; 95% CI = 1.4-4.9). Our data indicate that the -160 single nucleotide polymorphism in CDH1 is a low-penetrant prostate cancer susceptibility gene that might explain a proportion of familial and notably hereditary prostate cancer...
Familial prostate cancer and possible associated malignancies: nation-wide register cohort study in SwedenL Damber
Department of Oncology, Umea University, Sweden
Int J Cancer 78:293-7. 1998..Since no other malignancy was significantly associated with prostate cancer, it is most likely that familial prostate cancer is "site-specific"...
Estrogen receptor beta polymorphism is associated with prostate cancer riskCamilla Thellenberg-Karlsson
Department of Radiation Sciences Oncology, University of Umea, Umea, Sweden
Clin Cancer Res 12:1936-41. 2006..ERbeta is thought to exert an antiproliferative and proapoptotic effect. We examined whether sequence variants in the ERbeta gene are associated with prostate cancer risk...
H6D polymorphism in macrophage-inhibitory cytokine-1 gene associated with prostate cancerFredrik Lindmark
Department of Radiation Sciences Oncology, Umea University, Umea, Sweden
J Natl Cancer Inst 96:1248-54. 2004..We examined whether sequence variants in the MIC-1 gene are associated with the risk of prostate cancer...
Analysis of the macrophage scavenger receptor 1 gene in Swedish hereditary and sporadic prostate cancerFredrik Lindmark
Department of Radiation Sciences, Oncology, University of Umea, Umea, Sweden
Prostate 59:132-40. 2004..Here, we further elucidate the role of MSR1 in both Swedish families with HPC and in a cohort of unselected prostate cancer...
Prostate cancer in northern Sweden. Incidence, survival and mortality in relation to tumour gradeH Gronberg
Department of Oncology, University of Umea, Sweden
Acta Oncol 33:359-63. 1994..We believe that the most likely explanation for these changes in incidence, survival and mortality is enhanced detection of tumours with more favourable histology as a result of a more frequent use of the diagnostic tools available...
Association between the presence of bacterial 16S RNA in prostate specimens taken during transurethral resection of prostate and subsequent risk of prostate cancer (Sweden)O Alexeyev
Department of Medical Biosciences Pathology, Umea University, S 90185, Umea, Sweden
Cancer Causes Control 17:1127-33. 2006....
Germline mutations in E-cadherin do not explain association of hereditary prostate cancer, gastric cancer and breast cancerBjörn Anders Jonsson
Department of Medical Biosciences, Pathology, Umea University, Umea, Sweden
Int J Cancer 98:838-43. 2002..In a family with hereditary gastric cancer of the diffuse type, we identified the first truncating germline mutation in a Scandinavian family...
Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndromeK Cederquist
Medical and Clinical Genetics, Department of Medical Biosciences, Umea University, Sweden
Clin Genet 68:533-41. 2005..The several occurrences of breast cancer are not due to the MSH6 mutations. These findings are of great importance for counselling, management and surveillance of families with MSH6 mutations...
Germ-line genetic variation in the key androgen-regulating genes androgen receptor, cytochrome P450, and steroid-5-alpha-reductase type 2 is important for prostate cancer developmentSara Lindstrom
Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden
Cancer Res 66:11077-83. 2006..Carriers of five high-risk alleles in the AR, CYP17, and SRD5A2 genes are at approximately 2-fold excess risk to develop prostate cancer...
Linkage analysis of prostate cancer susceptibility: confirmation of linkage at 8p22-23Fredrik Wiklund
Department of Radiation Sciences, Oncology, University of Umea, 901 87 Umea, Sweden
Hum Genet 112:414-8. 2003..Thus, we have confirmed evidence for prostate cancer linkage at 8p22-23. Follow-up studies to evaluate the possible association between prostate cancer and genes in this region, especially the MSR1 gene, are warranted...
Comprehensive genetic evaluation of common E-cadherin sequence variants and prostate cancer risk: strong confirmation of functional promoter SNPSara Lindstrom
Department of Radiation Sciences, Oncology, University of Umea, 901 87, Umea, Sweden
Hum Genet 118:339-47. 2005..Due to the difficulties in replication of genetic association studies, this finding is unusual and novel...
Inherited variation in hormone-regulating genes and prostate cancer survivalSara Lindstrom
Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden
Clin Cancer Res 13:5156-61. 2007..However, little is known about genetic determinants of disease progression and prostate cancer-specific death...
Genetic analysis of the RNASEL gene in hereditary, familial, and sporadic prostate cancerFredrik Wiklund
Department of Radiation Sciences, Oncology, and Medical Biosciences, Pathology, University of Umea, Umea, Sweden
Clin Cancer Res 10:7150-6. 2004..To additionally evaluate the possible role of RNASEL in susceptibility to prostate cancer risk, we performed a comprehensive genetic analysis of sequence variants in RNASEL in the Swedish population...
Familial brain tumours-genetics or environment? A nationwide cohort study of cancer risk in spouses and first-degree relatives of brain tumour patientsBeatrice Malmer
Department of Radiation Sciences, Oncology, Umea University Hospital, Umea, Sweden
Int J Cancer 106:260-3. 2003..Spouses of PBT patients had an increased risk of skin cancer. We conclude that FDR, not spouses, have a significantly increased risk, which indicates a genetic origin of the familial aggregation of brain tumours...
The MTHFR 677C --> T polymorphism and risk of prostate cancer: results from the CAPS studyMattias Johansson
Department of Surgical and Perioperative Sciences, Urology and Andrology, Umea University Hospital, Umea 901 85, Sweden
Cancer Causes Control 18:1169-74. 2007..In conclusion, our results do not provide strong support for the hypothesis that the MTHFR 677C-->T polymorphism is related to prostate cancer risk...
Implications for prostate cancer of insulin-like growth factor-I (IGF-I) genetic variation and circulating IGF-I levelsMattias Johansson
Department of Surgical and Perioperative Sciences, Umea University Hospital, 901 85 Umea, Sweden
J Clin Endocrinol Metab 92:4820-6. 2007..We recently found a haplotype in the 3' region of the IGF-I gene associated with increased risk of prostate cancer, and we hypothesized that the observed association is mediated by circulating IGF-I...
Genome-wide scan of Swedish families with hereditary prostate cancer: suggestive evidence of linkage at 5q11.2 and 19p13.3Fredrik Wiklund
Department of Radiation Sciences, Oncology, University of Umea, Umea, Sweden
Prostate 57:290-7. 2003..Prostate cancer (CaP) is a common disorder with multiple genetic and environmental factors contributing to the disease. CaP susceptibility loci can be identified through genome-wide scans of high-risk families...
Second primary cancers in men with prostate cancer: an increased risk of male breast cancerCamilla Thellenberg
Department of Radiation Sciences, Oncology, , Sweden
J Urol 169:1345-8. 2003..To our knowledge these associations have not been reported previously, and they warrant more study...
Genetic variation in p53 and ATM haplotypes and risk of glioma and meningiomaBeatrice Susanne Malmer
Department of Radiation Sciences, Oncology, Umea University Hospital, 901 85, Umea, Sweden
J Neurooncol 82:229-37. 2007..Therefore, we tested the hypothesis that polymorphisms and haplotypes in p53 and ATM could be associated with glioma and meningioma risk...
Interleukin-1 receptor antagonist haplotype associated with prostate cancer riskF Lindmark
Department of Radiation Sciences Oncology, Umea University, Sweden
Br J Cancer 93:493-7. 2005....
Dietary supplement use patterns in men with prostate cancer: the Cancer Prostate Sweden studyA Westerlund
Division of Clinical Cancer Epidemiology, Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden
Ann Oncol 22:967-72. 2011..In a European setting, we know little about the use of dietary supplements among men with prostate cancer (PCa) and to what extent lifestyle, disease or other factors influence such use...
Genetic variation in the upstream region of ERG and prostate cancerSara Lindstrom
Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden
Cancer Causes Control 20:1173-80. 2009..Here, we investigated if inherited genetic variation upstream of ERG alters prostate cancer risk and survival...
A systematic overview of radiation therapy effects in rectal cancerBengt Glimelius
Department of Oncology, Radiology and Clinical Immunology, University Hospital, Uppsala, Sweden
Acta Oncol 42:476-92. 2003..The literature is inconclusive with respect to how frequently this occurs. Radiotherapy frequently produces symptom relief in patients with rectal cancer not amendable to surgery...
Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern SwedenKristina Cederquist
Unit of Medical and Clinical Genetics, Department of Medical Biosciences, Umea University, Sweden
Int J Cancer 109:370-6. 2004....
Systematic replication study of reported genetic associations in prostate cancer: Strong support for genetic variation in the androgen pathwaySara Lindstrom
Department of Radiation Sciences, Oncology, University of Umea, Umea, Sweden
Prostate 66:1729-43. 2006..Despite considerable efforts and initial promising findings, the field of prostate cancer genetics is characterized by inconclusive reports and no prostate cancer gene has yet been established...
Different aetiology of familial low-grade and high-grade glioma? A nationwide cohort study of familial gliomaBeatrice Malmer
Department of Radiation Sciences, Oncology, Umea University Hospital, Umea, Sweden
Neuroepidemiology 21:279-86. 2002..LGG families apparently have features manifesting a distinct pedigree pattern with sibpairs affected at a young age. These families could provide new insights into the aetiology of glioma...
Breast cancer as a second primary in patients with prostate cancer--estrogen treatment or association with family history of cancer?Camilla Thellenberg Karlsson
Department of Radiation Sciences, Oncology, University of Umea, Sweden
J Urol 176:538-43. 2006..In the current study we performed a comprehensive investigation of whether treatment for prostate cancer and/or family history is responsible for the excess risk...
Adjuvant chemotherapy in colorectal cancer: a joint analysis of randomised trials by the Nordic Gastrointestinal Tumour Adjuvant Therapy GroupBengt Glimelius
Department of Oncology, Radiology and Clinical Immunology, University Hospital, Uppsala, Sweden
Acta Oncol 44:904-12. 2005..15), favouring chemotherapy, was seen. The present analyses corroborate a small but clinically meaningful survival gain from adjuvant chemotherapy in colon cancer stage III, but not in the other presentations...
Does a low frequency of P53 and Pgp expression in familial glioma compared to sporadic controls indicate biological differences?Beatrice Malmer
Department of Radiation Sciences, Oncology, Umea University, 90187 Umea, Sweden
Anticancer Res 22:3949-54. 2002....
