利用传统和微阵列式比较基因组杂交确定与子宫颈内腺癌发生及转移相关的假想基因位点

来源 :世界核心医学期刊文摘(妇产科学分册) | 被引量 : 0次 | 上传用户:zhangxing0828
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Objectives This study aimed to estimate the gene loci associated with carcinogenesis of endocervical adenocarcinoma of uterus (EA) and metastasis. Study design Sixteen patients with EA were studied; 6 had nodal metastasis. DNA was extracted from EAs, and subjected to both conventional comparative genomic hybridization (CGH) and arraybased CGH. Copy number abnormalities were compared between cases with and without nodal metastasis. Results In all EAs, high frequencies of copy number losses were detected in genes LRP1B (on 2q21.2)-, DAB2 (5p13), and DCC (18q21.3), as well as regions 3p, 16q, and 22q, and copy number amplifications in genes NRAS (1p13.2), TOP2A (17q21-q22), NCOA3(AIB1) (20q12), and ARSA (22q tel). Nodal metastasis was associated with high frequencies of copy number loss in genes PGRMC2 and LAMA3 and amplification in CDK6 and NCOA3(AIB1). Conclusion This is the first report of gene copy number alterations spanning the whole genome in EA. These altered genes are speculated to be associated with EAs as a tumor suppressor and/or oncogene. Objectives This study aimed to estimate the gene loci associated with carcinogenesis of endocervical adenocarcinoma of uterus (EA) and metastasis. Study design Sixteen patients with EA were studied; 6 had nodal metastasis. DNA was extracted from EAs, and subjected to both conventional Hybridization (CGH) and arraybased CGH. Copy number abnormalities were compared between cases with and without nodal metastasis. Results In all EAs, high frequencies of copy number losses were detected in genes LRP1B (on 2q21.2) -, DAB2 (5p13 ), and DCC (18q21.3), as well as regions 3p, 16q, and 22q, and copy number amplifications in genes NRAS (1p13.2), TOP2A (17q21- q22), NCOA3 (AIB1) ARSA (22q tel). Nodal metastasis was associated with high frequencies of copy number loss in genes PGRMC2 and LAMA3 and amplification in CDK6 and NCOA3 (AIB1). Conclusion This is the first report of gene copy number alterations spanning the whole genome in EA. These altered genes are speculat ed to be associated with EAs as a tumor suppressor and / or oncogene.
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