Hunt Erin N, Kopacz Jonathan P, Vestal Deborah J
Department of Biological Sciences, University of Toledo, Toledo, OH 43606, USA.
Cancers (Basel). 2022 Jun 4;14(11):2794. doi: 10.3390/cancers14112794.
At least one member of the Guanylate-Binding Protein (GBP) family of large interferon-induced GTPases has been classified as both a marker of good prognosis and as a potential drug target to treat breast cancers. However, the activity of individual GBPs appears to not just be tumor cell type-specific but dependent on the growth factor and/or cytokine environment in which the tumor cells reside. To clarify what we do and do not know about GBPs in breast cancer, the current literature on GBP-1, GBP-2, and GBP-5 in breast cancer has been assembled. In addition, we have analyzed the role of each of these GBPs in predicting recurrence-free survival (RFS), overall survival (OS), and distance metastasis-free survival (DMFS) as single gene products in different subtypes of breast cancers. When a large cohort of breast cancers of all types and stages were examined, GBP-1 correlated with poor RFS. However, it was the only GBP to do so. When smaller cohorts of breast cancer subtypes grouped into ER+, ER+/HER2-, and HER2+ tumors were analyzed, none of the GBPs influenced RFS, OS, or DMSF as single agents. The exception is GBP-5, which correlated with improved RFS in HER2+ breast cancers. All three GBPs individually predicted improved RFS, OS, and DMSF in ER- breast cancers, regardless of the PR or HER2 status, and TNBCs.
鸟苷酸结合蛋白(GBP)家族是一类由干扰素诱导产生的大型GTP酶,其中至少有一个成员已被归类为乳腺癌良好预后的标志物和潜在的治疗靶点。然而,单个GBP的活性似乎不仅具有肿瘤细胞类型特异性,还取决于肿瘤细胞所处的生长因子和/或细胞因子环境。为了厘清我们对乳腺癌中GBP的了解与未知,我们汇集了目前关于乳腺癌中GBP-1、GBP-2和GBP-5的文献。此外,我们分析了这些GBP中的每一个作为单一基因产物在不同亚型乳腺癌中预测无复发生存期(RFS)、总生存期(OS)和无远处转移生存期(DMFS)的作用。当对所有类型和阶段的大量乳腺癌队列进行检查时,GBP-1与较差的RFS相关。然而,它是唯一有此关联的GBP。当对分为雌激素受体阳性(ER+)、雌激素受体阳性/人表皮生长因子受体2阴性(ER+/HER2-)和人表皮生长因子受体2阳性(HER2+)肿瘤的较小乳腺癌亚型队列进行分析时,没有一个GBP作为单一因子影响RFS、OS或DMSF。例外的是GBP-5,它与HER2+乳腺癌中改善的RFS相关。无论孕激素受体(PR)或HER2状态如何,以及三阴性乳腺癌(TNBC),所有这三种GBP单独都能预测ER-乳腺癌中改善的RFS、OS和DMSF。