Transcription profiling of mouse mammary tumors from animals which have exons 4-7 of the Lkb1 gene deleted
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ABSTRACT: Heterozygous germ-line mutations in the LKB1 (STK11) gene cause Peutz-Jeghers syndrome (PJS), an autosomal dominant disorder characterized by hamartomatous polyposis of the gastrointestinal tract and an increased risk of colorectal, breast, ovarian, testicular and cervical cancer. To model the effects of LKB1 mutation in mammary tumourigenesis, we have used a conditional gene targeting strategy to generate a mouse in which exons 4-7 of the Lkb1 gene encoding the kinase domain of the protein are deleted specifically in the mammary gland. Mammary gland tumours arise in these mice with a latency of 46-85 weeks and occur in the thoracic or inguinal glands. These mammary gland tumours were characterised as Grade 2 invasive ductal carcinomas or solid papillary carcinomas and resemble those arisi
ORGANISM(S): Mus musculus
SUBMITTER: Anita Grigoriadis
PROVIDER: E-TABM-643 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
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