• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

PLPP2:PLPP 家族中乳腺癌的潜在治疗靶点。

PLPP2: Potential therapeutic target of breast cancer in PLPP family.

机构信息

Weifang People's Hospital, 261000 Weifang, China.

School of Basic Medicine, Weifang Medical University, 261053 Weifang, China.

出版信息

Immunobiology. 2022 Nov;227(6):152298. doi: 10.1016/j.imbio.2022.152298. Epub 2022 Oct 28.

DOI:10.1016/j.imbio.2022.152298
PMID:36332491
Abstract

PLPPs (Phospholipid phosphatases) are widely expressed in different human tissues, regulate cell signal transduction, and are overexpressed in cancers such as gliomas, pancreatic adenocarcinoma, lung adenocarcinoma, and so on. As a member of the PLPP family, PLPP2 (phospholipid phosphatase 2) plays a vital role in the occurrence and development of breast cancer, but its mechanism is still unclear. Our research found that PLPP2 was overexpressed in breast cancer, and the higher expression level of PLPP2 showed a worse prognosis for breast cancer patients. Further analysis showed that overexpression of PLPP2 affected the expression of CDC34 (cell-division cycle 34), LSM7 (Like-Smith 7), and SGTA (small glutamine-rich tetratricopeptide repeat-containing protein alpha) through EMT (epigenetic-mesenchymal transition) related pathways to promote the occurrence and development of breast cancer. In vitro, silencing PLPP2 significantly reduced the proliferation, invasion, and migration abilities of human breast cancer cells MDA-MB-231. ER+ is a common subtype of breast cancer. Furthermore, we found that the overexpression of PLPP2 was significantly related to the poor prognosis of ER+ breast cancer. These results indicate that PLPP2 has value as a potential therapeutic target for breast cancer, especially for ER+ breast cancer.

摘要

PLPPs(磷脂磷酸酶)广泛表达于不同的人体组织中,调节细胞信号转导,在神经胶质瘤、胰腺腺癌、肺腺癌等癌症中过度表达。PLPP2(磷脂磷酸酶 2)作为 PLPP 家族的一员,在乳腺癌的发生发展中起着至关重要的作用,但作用机制尚不清楚。我们的研究发现 PLPP2 在乳腺癌中过表达,PLPP2 表达水平越高,乳腺癌患者的预后越差。进一步分析表明,PLPP2 的过表达通过 EMT(表观遗传-间质转化)相关途径影响 CDC34(细胞分裂周期 34)、LSM7(Like-Smith 7)和 SGTA(小谷氨酰胺富含四肽重复蛋白 alpha)的表达,从而促进乳腺癌的发生和发展。在体外,沉默 PLPP2 显著降低了人乳腺癌细胞 MDA-MB-231 的增殖、侵袭和迁移能力。ER+是乳腺癌的常见亚型。此外,我们发现 PLPP2 的过表达与 ER+乳腺癌患者的不良预后显著相关。这些结果表明,PLPP2 作为一种潜在的乳腺癌治疗靶点具有价值,特别是对 ER+乳腺癌。

相似文献

1
PLPP2: Potential therapeutic target of breast cancer in PLPP family.PLPP2:PLPP 家族中乳腺癌的潜在治疗靶点。
Immunobiology. 2022 Nov;227(6):152298. doi: 10.1016/j.imbio.2022.152298. Epub 2022 Oct 28.
2
Transcriptomic landscape based on annotated clinical features reveals PLPP2 involvement in lipid raft-mediated proliferation signature of early-stage lung adenocarcinoma.基于注释临床特征的转录组景观揭示 PLPP2 参与早期肺腺癌脂筏介导的增殖特征。
J Exp Clin Cancer Res. 2023 Nov 23;42(1):315. doi: 10.1186/s13046-023-02877-w.
3
miR-381 inhibited breast cancer cells proliferation, epithelial-to-mesenchymal transition and metastasis by targeting CXCR4.miR-381 通过靶向 CXCR4 抑制乳腺癌细胞增殖、上皮间质转化和转移。
Biomed Pharmacother. 2017 Feb;86:426-433. doi: 10.1016/j.biopha.2016.12.051. Epub 2016 Dec 21.
4
Glypican-3 induces a mesenchymal to epithelial transition in human breast cancer cells.磷脂酰肌醇蛋白聚糖-3可诱导人乳腺癌细胞发生间充质向上皮转化。
Oncotarget. 2016 Sep 13;7(37):60133-60154. doi: 10.18632/oncotarget.11107.
5
BRD7 suppresses invasion and metastasis in breast cancer by negatively regulating YB1-induced epithelial-mesenchymal transition.BRD7 通过负向调控 YB1 诱导的上皮-间充质转化抑制乳腺癌的侵袭和转移。
J Exp Clin Cancer Res. 2020 Feb 7;39(1):30. doi: 10.1186/s13046-019-1493-4.
6
Possible involvement of TGF‑β‑SMAD‑mediated epithelial‑mesenchymal transition in pro‑metastatic property of PAX6.PAX6 促进转移的特性可能涉及 TGF-β-SMAD 介导的上皮间质转化。
Oncol Rep. 2020 Aug;44(2):555-564. doi: 10.3892/or.2020.7644. Epub 2020 Jun 11.
7
Molecular mechanism of miR-153 inhibiting migration, invasion and epithelial-mesenchymal transition of breast cancer by regulating transforming growth factor beta (TGF-β) signaling pathway.miR-153 通过调控转化生长因子 β(TGF-β)信号通路抑制乳腺癌迁移、侵袭及上皮间质转化的分子机制。
J Cell Biochem. 2019 Jun;120(6):9539-9546. doi: 10.1002/jcb.28230. Epub 2018 Dec 7.
8
Overexpression of microRNA-190 inhibits migration, invasion, epithelial-mesenchymal transition, and angiogenesis through suppression of protein kinase B-extracellular signal-regulated kinase signaling pathway via binding to stanniocalicin 2 in breast cancer.microRNA-190 的过表达通过与乳腺癌中的 stanniocalcin 2 结合抑制蛋白激酶 B-细胞外信号调节激酶信号通路,从而抑制迁移、侵袭、上皮间质转化和血管生成。
J Cell Physiol. 2019 Aug;234(10):17824-17838. doi: 10.1002/jcp.28409. Epub 2019 Apr 16.
9
Cyclin D1, Id1 and EMT in breast cancer.细胞周期蛋白 D1、Id1 和 EMT 在乳腺癌中的作用。
BMC Cancer. 2011 Sep 28;11:417. doi: 10.1186/1471-2407-11-417.
10
Notch1 signaling regulates the epithelial-mesenchymal transition and invasion of breast cancer in a Slug-dependent manner.Notch1信号通路以依赖Slug的方式调节乳腺癌的上皮-间质转化和侵袭。
Mol Cancer. 2015 Feb 3;14(1):28. doi: 10.1186/s12943-015-0295-3.

引用本文的文献

1
Silencing PPAP2C inhibits lung adenocarcinoma migration and invasion via the ERK/JNK pathway.沉默 PPAP2C 通过 ERK/JNK 通路抑制肺腺癌迁移和侵袭。
Mol Med Rep. 2025 Jan;31(1). doi: 10.3892/mmr.2024.13392. Epub 2024 Nov 14.
2
Transcriptomic landscape based on annotated clinical features reveals PLPP2 involvement in lipid raft-mediated proliferation signature of early-stage lung adenocarcinoma.基于注释临床特征的转录组景观揭示 PLPP2 参与早期肺腺癌脂筏介导的增殖特征。
J Exp Clin Cancer Res. 2023 Nov 23;42(1):315. doi: 10.1186/s13046-023-02877-w.