Research Topics
Species | S A GaytherSummaryAffiliation: University of Cambridge Country: UK Publications
| Collaborators
|
Detail Information
Publications
The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genesS A Gayther
Department of Oncology, Cancer Research Campaign, Strangeways Research Laboratory, Cambridge, United Kingdom
Am J Hum Genet 65:1021-9. 1999..We discuss the implications for genetic testing and clinical management of familial ovarian cancer arising from the data presented in these studies...
The genetics of inherited breast cancerS A Gayther
CRC Human Cancer Genetics Research Group, Addenbrooke s Hospital, Cambridge, United Kingdom
J Mammary Gland Biol Neoplasia 3:365-76. 1998..We review the evidence for gene-gene and gene-environment interaction in modifying that risk, and discuss the contribution of BRCA1 and BRCA2 and other high penetrance genes to both inherited and sporadic breast cancer...
Frequent loss of BRCA1 mRNA and protein expression in sporadic ovarian cancersP A Russell
CRC Department of Oncology, Strangeways Research Laboratory, Cambridge, UK
Int J Cancer 87:317-21. 2000..Together, these data suggest that expression of BRCA1 is down-regulated at the level of transcription during the development of sporadic ovarian cancers...
Risk models for familial ovarian and breast cancerA C Antoniou
CRC Genetic Epidemiology Unit, Institute of Public Health, University of Cambridge, Cambridge, United Kingdom
Genet Epidemiol 18:173-90. 2000..The high penetrance estimate for ovarian cancer, compared with other studies, suggests that modifying genetic or environmental factors may be important determinants of risk...
Mutations truncating the EP300 acetylase in human cancersS A Gayther
Department of Oncology, University of Cambridge, Cambridge, UK
Nat Genet 24:300-3. 2000..Our data show that EP300 is mutated in epithelial cancers and provide the first evidence that it behaves as a classical tumour-suppressor gene...
Apparent human BRCA1 knockout caused by mispriming during polymerase chain reaction: implications for genetic testingB Kuschel
CRC Human Cancer Genetics Research Group, Department of Oncology, Strangeways Research Laboratories, Cambridge, England
Genes Chromosomes Cancer 31:96-8. 2001..This may have major implications for the sensitivity of all polymerase chain reaction-based mutation-detection methods in clinical genetic testing laboratories...
A gene (DLG2) located at 17q12-q21 encodes a new homologue of the Drosophila tumor suppressor dIg-AS Mazoyer
CRC Human Cancer Genetics Research Group, Addenbrooke s Hospital, Cambridge, United Kingdom
Genomics 28:25-31. 1995..No evidence for mutation was found, making it unlikely that DLG2 is involved in sporadic breast cancer...
Aberrant splicing of the TSG101 and FHIT genes occurs frequently in multiple malignancies and in normal tissues and mimics alterations previously described in tumoursS A Gayther
CRC Human Cancer Genetics Research Group, Addenbrooke s Hospital, Cambridge, UK
Oncogene 15:2119-26. 1997..While we cannot exclude that alterations in TSG101 and FHIT occur during cancer development, our data indicate that in this context the commonly observed transcript abnormalities are misleading...
Frequently occurring germ-line mutations of the BRCA1 gene in ovarian cancer families from RussiaS A Gayther
Am J Hum Genet 60:1239-42. 1997
Identification of germ-line E-cadherin mutations in gastric cancer families of European originS A Gayther
Department of Oncology and Cancer Research Campaign Human Cancer Genetics Research Group, University of Cambridge, Addenbrooke s Hospital, United Kingdom
Cancer Res 58:4086-9. 1998..Here, we show that a proportion of diffuse gastric cancer families of European origin have germ-line E-cadherin mutations; however, these mutations are absent in intestinal gastric cancer families...
Somatic mitochondrial DNA mutations in primary and metastatic ovarian cancerP O Van Trappen
Gynaecological Cancer Centre and Centre for Translational Oncology, Institute of Cancer and CR UK Clinical Centre, Barts and The London, Queen Mary s School of Medicine and Dentistry, John Vane Science Centre, London, UK
Gynecol Oncol 104:129-33. 2007..To establish whether different mtDNA variants can be found in the same cancer but at different sites, we analyzed a series of unilateral and bilateral primary epithelial ovarian cancers as well as paired metastatic tumor deposits...
Genetic intra-tumour heterogeneity in epithelial ovarian cancer and its implications for molecular diagnosis of tumoursL Khalique
Translational Research Laboratory, Department of Gynaecological Oncology, Institute for Women s Health, University College London, UK
J Pathol 211:286-95. 2007..The basis of genetic ITH and the possible implications for molecular approaches to clinical diagnosis of ovarian cancers may apply to other tumour types...
Human ovarian surface epithelial cells immortalized with hTERT maintain functional pRb and p53 expressionN F Li
Centre for Translational Oncology, Barts and The London, Queen Mary s School of Medicine and Dentistry, Charterhouse Square, London, UK
Cell Prolif 40:780-94. 2007..Establishment of immortalized OSE cell lines has, in the past, required inactivation of pRb and p53 functions. However, this often leads to increased chromosome instability during prolonged culture...
Grading of serous ovarian carcinoma: further evidence of a lack of agreement between conventional grading systemsN Singh
Histopathology 52:393-5. 2008
Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the Ovarian Cancer Association Consortium pooled analysisC L Pearce
Department of Preventive Medicine, Keck School of Medicine, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA 90089, USA
Br J Cancer 98:282-8. 2008..80, 95% CI 0.62-1.04, P=0.100). These data suggest that while these three variants in the PGR are not associated with ovarian cancer overall, the PROGINS variant may play a modest role in risk of endometrioid ovarian cancer...
