To determine sequence variations of the BUB1 and BUB1B genes in pancreatic cancer, the entire coding regions of the BUB1 and BUB1B genes were sequenced in pancreatic cancer cell lines and xenografts. Although only polymorphic alterations were found in the BUB1B gene, the aneuploid pancreatic cell li
A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene
✍ Scribed by José Adélaïde; Huai-En Huang; Anne Murati; Amber E. Alsop; Béatrice Orsetti; Marie-Joëlle Mozziconacci; Cornel Popovici; Christophe Ginestier; Anne Letessier; Céline Basset; Céline Courtay-Cahen; Jocelyne Jacquemier; Charles Theillet; Daniel Birnbaum; Paul A.W. Edwards; Max Chaffanet
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 393 KB
- Volume
- 37
- Category
- Article
- ISSN
- 1045-2257
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✦ Synopsis
Abstract
The 8p11–21 region is a frequent target of alterations in breast cancer and other carcinomas. We surveyed 34 breast tumor cell lines and 9 pancreatic cancer cell lines for alterations of this region by use of multicolor fluorescence in situ hybridization (M‐FISH) and BAC‐specific FISH. We describe a recurrent chromosome translocation breakpoint that targets the NRG1 gene on 8p12. NRG1 encodes growth factors of the neuregulin/heregulin‐1 family that are ligands for tyrosine kinase receptors of the ERBB family. Breakpoints within the NRG1 gene were found in four of the breast tumor cell lines: ZR‐75‐1, in a dic(8;11); HCC1937, in a t(8;10)(p12;p12.1); SUM‐52, in an hsr(8)(p12); UACC‐812, in a t(3;8); and in two of the pancreatic cancer cell lines: PaTu I, in a der(8)t(4;8); and SUIT‐2, in a del(8)(p). Mapping by two‐color FISH showed that the breaks were scattered over 1.1 Mb within the NRG1 gene. It is already known that the MDA‐MB‐175 breast tumor cell line has a dic(8;11), with a breakpoint in NRG1 that fuses NRG1 to the DOC4 gene on 11q13. Thus, we have found a total of seven breakpoints, in two types of cancer cell lines, that target the NRG1 gene. This suggests that the NRG1 locus is a recurring target of translocations in carcinomas. PCR analysis of reverse‐transcribed cell line RNAs revealed an extensive complexity of the NRG1 transcripts but failed to detect a consistent pattern of mRNA isoforms in the cell lines with NRG1 breakpoint. © 2003 Wiley‐Liss, Inc.
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