Membrane localization of insulin receptor substrate-2 (IRS-2) is associated with decreased overall survival in breast cancer

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作者
Jennifer L. Clark
Karen Dresser
Chung-Cheng Hsieh
Michael Sabel
Celina G. Kleer
Ashraf Khan
Leslie M. Shaw
机构
[1] University of Massachusetts Medical School,Department of Cancer Biology
[2] University of Massachusetts Medical School,Department of Pathology
[3] University of Michigan Health System,Department of Surgery
[4] University of Michigan Health System,Department of Pathology
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IRS proteins; Breast cancer; Progesterone receptor; IGF-1 receptor;
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摘要
Recent studies have identified a role for insulin receptor substrate-2 (IRS-2) in promoting motility and metastasis in breast cancer. However, no published studies to date have examined IRS-2 expression in human breast tumors. We examined IRS-2 expression by immunohistochemistry (IHC) in normal breast tissue, benign breast lesions, and malignant breast tumors from the institutional pathology archives and a tumor microarray from a separate institution. Three distinct IRS-2 staining patterns were noted: diffusely cytoplasmic, punctate cytoplasmic, and localized to the cell membrane. The individual and pooled datasets were analyzed for associations of IRS-2 staining pattern with core clinical parameters and clinical outcomes. Univariate analysis revealed a trend toward decreased overall survival (OS) with IRS-2 membrane staining, and this association became significant upon multivariate analysis (P = 0.01). In progesterone receptor negative (PR−) tumors, in particular, IRS-2 staining at the membrane correlated with significantly worse OS than other IRS-2 staining patterns (P < 0.001). When PR status and IRS-2 staining pattern were evaluated in combination, PR− tumors with IRS-2 at the membrane were associated with a significantly decreased OS when compared with all other combinations (P = 0.002). Evaluation of IRS-2 staining patterns could potentially be used to identify patients with PR− tumors who would most benefit from aggressive treatment.
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页码:759 / 772
页数:13
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