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FGFR1copy number in breast cancer: associations with proliferation, histopathological grade and molecular subtypes

乳腺癌 拷贝数变化 成纤维细胞生长因子受体1 拷贝数分析 生物 癌症 癌症研究 医学 肿瘤科 内科学 基因 遗传学 受体 成纤维细胞生长因子 基因组
作者
Anna Mary Bofin,Borgny Ytterhus,Elise Klæstad,Marit Valla
出处
期刊:Journal of Clinical Pathology [BMJ]
卷期号:75 (7): 459-464 被引量:5
标识
DOI:10.1136/jclinpath-2021-207456
摘要

FGFR1 is located on 8p11.23 and regulates cell proliferation and survival. Increased copy number of FGFR1 is found in several cancers including cancer of the breast. ZNF703 is located close to FGFR1 at 8p11-12 and is frequently expressed in the luminal B subtype of breast cancer. Using tissue samples from a well-described cohort of patients with breast cancer with long-term follow-up, we studied associations between FGFR1 copy number in primary breast cancer tumours and axillary lymph node metastases, and proliferation status, molecular subtype and prognosis. Furthermore, we studied associations between copy number increase of FGFR1 and copy number of ZNF703.We used fluorescence in situ hybridisation for FGFR1 and the chromosome 8 centromere applied to tissue microarray sections from a series of 534 breast cancer cases.We found increased copy number (≥4) of FGFR1 in 74 (13.9%) of tumours. Only 6 of the 74 cases with increased copy number were non-luminal. Increased FGFR1 copy number was significantly associated with high Ki-67 status, high mitotic count and high histopathological grade, but not with prognosis. Forty-two (7.9%) cases had mean copy number ≥6. Thirty of these showed ZNF708 copy number ≥6.Our results show that FGFR1 copy number increase is largely found among luminal subtypes of breast cancer, particularly luminal B (HER2-). It is frequently accompanied by increased copy number of ZNF703. FGFR1 copy number increase is associated with high histopathological grade and high proliferation. However, we did not discover an association with prognosis.
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