TY - JOUR
T1 - Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies within the BRCA2 region
AU - Schutte, Mieke
AU - Da Costa, Luis T.
AU - Hahn, Stephan A.
AU - Moskaluk, Chris
AU - Hoque, A. T.M.Shamsul
AU - Rozenblum, Ester
AU - Weinstein, Craig L.
AU - Bittner, Michael
AU - Meltzer, Paul S.
AU - Trent, Jeffrey M.
AU - Yeo, Charles J.
AU - Hruban, Ralph H.
AU - Kern, Scott E.
PY - 1995/6/20
Y1 - 1995/6/20
N2 - Homozygous deletions have been central to the discovery of several tumor- suppressor genes, but their finding has often been either serendipitous or the result of a directed search. A recently described technique [Lisitsyn, N., Lisitsyn, N. and Wigler, M. (1993) Science 259, 946-951] held out the potential to efficiently discover such events in an unbiased manner. Here we present the application of the representational difference analysis (RDA) to the study of cancer. We cloned two DNA fragments that identified a homozygous deletion in a human pancreatic adenocarcinoma, mapping to a 1-centimorgan region at chromosome 13q12.3 flanked by the markers D13S171 and D13S260. Interestingly, this lies within the 6-centimorgan region recently identified as the BRCA2 locus of heritable breast cancer susceptibility. This suggests that the same gene may be involved in multiple tumor types and that its function is that of a tumor suppressor rather than that of a dominant oncogene.
AB - Homozygous deletions have been central to the discovery of several tumor- suppressor genes, but their finding has often been either serendipitous or the result of a directed search. A recently described technique [Lisitsyn, N., Lisitsyn, N. and Wigler, M. (1993) Science 259, 946-951] held out the potential to efficiently discover such events in an unbiased manner. Here we present the application of the representational difference analysis (RDA) to the study of cancer. We cloned two DNA fragments that identified a homozygous deletion in a human pancreatic adenocarcinoma, mapping to a 1-centimorgan region at chromosome 13q12.3 flanked by the markers D13S171 and D13S260. Interestingly, this lies within the 6-centimorgan region recently identified as the BRCA2 locus of heritable breast cancer susceptibility. This suggests that the same gene may be involved in multiple tumor types and that its function is that of a tumor suppressor rather than that of a dominant oncogene.
UR - http://www.scopus.com/inward/record.url?scp=0029041032&partnerID=8YFLogxK
U2 - 10.1073/pnas.92.13.5950
DO - 10.1073/pnas.92.13.5950
M3 - Article
C2 - 7597059
AN - SCOPUS:0029041032
SN - 0027-8424
VL - 92
SP - 5950
EP - 5954
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 13
ER -