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POPDC1 在人乳腺癌组织中受到抑制,并在乳腺癌细胞系中受到 EGFR 的负调控。

POPDC1 is suppressed in human breast cancer tissues and is negatively regulated by EGFR in breast cancer cell lines.

机构信息

School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, Scotland, United Kingdom.

出版信息

Cancer Lett. 2017 Oct 10;406:81-92. doi: 10.1016/j.canlet.2017.08.002. Epub 2017 Aug 12.

Abstract

Breast cancer molecular heterogeneity has resulted in disparities in therapeutic response and targeting of molecular subtypes of breast cancer. This necessitates identification and validation of novel therapeutic targets for breast cancer treatment. Suppression of Popeye domain-containing (POPDC) proteins is hypothesized to promote malignant cell behaviour and poor clinical outcomes in various cancers. We aimed to determine whether POPDC proteins are suppressed in human ductal carcinoma tissues and if this correlates to clinical progression and Her2 status. We further assessed if the EGFR regulated POPDC1 in breast cancer. Here we show significant suppression of POPDC1 in malignant breast cancer tissues without correlation to clinical progression. Interestingly, POPDC2 and POPDC3 were highly expressed in malignant breast tissues. Furthermore, HER2+ status significantly correlated with high POPDC2 and POPDC3, but not POPDC1 expression. We further show for the first time that low POPDC1 correlates to high EGFR expression in breast cancer tissues and that EGFR negatively regulates POPDC1 expression in MCF7, MDA231 and SKBR3 breast cancer cells. Furthermore, overexpression of POPDC1 in MCF7, MDA231 and SKBR3 cells attenuated EGF-mediated cell migration and proliferation. These findings show that POPDC1 is suppressed in breast cancer and can potentially be targeted to inhibit EGFR-mediated cell migration and proliferation.

摘要

乳腺癌分子异质性导致了治疗反应和针对乳腺癌分子亚型的靶向治疗的差异。这就需要确定和验证乳腺癌治疗的新的治疗靶点。抑制 Popeye 结构域蛋白(POPDC)被假设为促进各种癌症中的恶性细胞行为和不良临床结局。我们旨在确定 POPDC 蛋白是否在人导管癌组织中受到抑制,以及这是否与临床进展和 Her2 状态相关。我们进一步评估了 EGFR 是否调节了乳腺癌中的 POPDC1。在这里,我们显示 POPDC1 在恶性乳腺癌组织中显著受到抑制,与临床进展无关。有趣的是,POPDC2 和 POPDC3 在恶性乳腺组织中高度表达。此外,HER2+状态与高 POPDC2 和 POPDC3 显著相关,但与 POPDC1 无关。我们还首次表明,乳腺癌组织中低 POPDC1 与高 EGFR 表达相关,并且 EGFR 负调节 MCF7、MDA231 和 SKBR3 乳腺癌细胞中的 POPDC1 表达。此外,在 MCF7、MDA231 和 SKBR3 细胞中过表达 POPDC1 可减弱 EGF 介导的细胞迁移和增殖。这些发现表明 POPDC1 在乳腺癌中受到抑制,并且可以作为抑制 EGFR 介导的细胞迁移和增殖的潜在靶点。

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