Loss of heterozygosity occurs at the d11s29 locus on chromosome 11q23 in invasive cervical carcinoma


Play all audios:

Loading...

ABSTRACT Allelotypic detection of loss of heterozygosity (LOH) has been used to identify putative tumour-suppressor genes. Loci on human chromosome 11q23 are frequently altered in malignant


disease, and LOH has been reported at an anonymous D11S29 locus at 11q23 in a proportion of breast and ovarian cancers and malignant melanomas. Previous studies have reported a high


frequency of LOH in cervical carcinoma mapping to 11q23. Using polymerase chain reaction techniques employing probes for a recently described polymorphic dinucleotide microsatellite within


this locus, we have searched for LOH in 69 cases of invasive cervical carcinoma. Genomic material was microdissected from sections cut from archival paraffin-embedded material, using the


patients' constitutional genotype as a control Sixty-two (90%) of the cases were informative, and LOH occurred in 25/62 (40%) of tumours. Loss of an arm or single chromosome 11 is a


well-recognised event in cervical carcinoma, and by employing other microsatellite polymorphisms mapping to 11q13 and 11p11-p12 we excluded those cases with widespread allelic loss. By doing


so, LOH at D11S29 was found in 16/53 (30%) of tumours. The findings suggest a putative tumour-suppressor gene on 11q involved in cervical carcinogenesis. Access through your institution Buy


or subscribe This is a preview of subscription content, access via your institution ACCESS OPTIONS Access through your institution Subscribe to this journal Receive 24 print issues and


online access $259.00 per year only $10.79 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access to full article PDF Buy now Prices may be subject to local taxes


which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs * Contact customer support SIMILAR CONTENT BEING VIEWED BY


OTHERS SCRAMBLING THE GENOME IN CANCER: CAUSES AND CONSEQUENCES OF COMPLEX CHROMOSOME REARRANGEMENTS Article 08 November 2023 LUMINAL BREAST EPITHELIAL CELLS OF _BRCA1_ OR _BRCA2_ MUTATION


CARRIERS AND NONCARRIERS HARBOR COMMON BREAST CANCER COPY NUMBER ALTERATIONS Article Open access 20 November 2024 PERVASIVE CHROMOSOMAL INSTABILITY AND KARYOTYPE ORDER IN TUMOUR EVOLUTION


Article 02 September 2020 AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Nuffield Department of Pathology and Bacteriology, University of Oxford, John Radcliffe Hospital, UK PB Bethwaite


Authors * PB Bethwaite View author publications You can also search for this author inPubMed Google Scholar * J Koreth View author publications You can also search for this author inPubMed 


Google Scholar * CS Herrington View author publications You can also search for this author inPubMed Google Scholar * JO'D McGee View author publications You can also search for this


author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Bethwaite, P., Koreth, J., Herrington, C. _et al._ Loss of heterozygosity


occurs at the D11S29 locus on chromosome 11q23 in invasive cervical carcinoma. _Br J Cancer_ 71, 814–818 (1995). https://doi.org/10.1038/bjc.1995.157 Download citation * Issue Date: 01 April


1995 * DOI: https://doi.org/10.1038/bjc.1995.157 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is


not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative