• 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

AG-205 可独立于 PGRMC1 和相关 MAPR 蛋白上调人子宫内膜细胞中胆固醇生物合成和类固醇生成相关的酶。

AG-205 Upregulates Enzymes Involved in Cholesterol Biosynthesis and Steroidogenesis in Human Endometrial Cells Independently of PGRMC1 and Related MAPR Proteins.

机构信息

CELL Unit, de Duve Institute and Université Catholique de Louvain, B-1200 Brussels, Belgium.

GEPI Unit, de Duve Institute and Université Catholique de Louvain, B-1200 Brussels, Belgium.

出版信息

Biomolecules. 2021 Oct 6;11(10):1472. doi: 10.3390/biom11101472.

DOI:10.3390/biom11101472
PMID:34680104
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8533447/
Abstract

An inappropriate response to progestogens in the human endometrium can result in fertility issues and jeopardize progestin-based treatments against pathologies such as endometriosis. PGRMC1 can mediate progesterone response in the breast and ovaries but its endometrial functions remain unknown. AG-205 is an alleged PGRMC1 inhibitor but its specificity was recently questioned. We added AG-205 in the cultures of two endometrial cell lines and performed a transcriptomic comparison. AG-205 significantly increased expression of genes coding enzymes of the cholesterol biosynthetic pathway or of steroidogenesis. However, these observations were not reproduced with cells transfected with siRNA against PGRMC1 or its related proteins (MAPRs). Furthermore, AG-205 retained its ability to increase expression of selected target genes even when expression of PGRMC1 or all MAPRs was concomitantly downregulated, indicating that neither PGRMC1 nor any MAPR is required to mediate AG-205 effect. In conclusion, although AG-205 has attractive effects encouraging its use to develop therapeutic strategies, for instance against breast cancer, our study delivers two important warning messages. First, AG-205 is not specific for PGRMC1 or other MAPRs and its mechanisms of action remain unclear. Second, due to its effects on genes involved in steroidogenesis, its use may increase the risk for endometrial pathologies resulting from imbalanced hormones concentrations.

摘要

人类子宫内膜对孕激素的反应不当可能导致生育问题,并危及孕激素为基础的治疗方法,如子宫内膜异位症。PGRMC1 可以介导孕激素在乳腺和卵巢中的反应,但它在子宫内膜中的功能仍然未知。AG-205 是一种据称的 PGRMC1 抑制剂,但最近其特异性受到质疑。我们在两种子宫内膜细胞系的培养物中添加了 AG-205,并进行了转录组比较。AG-205 显著增加了编码胆固醇生物合成途径或类固醇生成酶的基因的表达。然而,用针对 PGRMC1 或其相关蛋白 (MAPRs) 的 siRNA 转染的细胞并未重现这些观察结果。此外,即使同时下调 PGRMC1 或所有 MAPRs 的表达,AG-205 仍保留其增加选定靶基因表达的能力,表明介导 AG-205 作用既不需要 PGRMC1 也不需要任何 MAPR。总之,尽管 AG-205 具有令人鼓舞的作用,鼓励其用于开发治疗策略,例如治疗乳腺癌,但我们的研究提供了两个重要的警告信息。首先,AG-205 对 PGRMC1 或其他 MAPRs 并不特异,其作用机制仍不清楚。其次,由于其对参与类固醇生成的基因的影响,其使用可能会增加由于激素浓度失衡而导致的子宫内膜病变的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/3b48221dacc8/biomolecules-11-01472-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/53f4ee740f99/biomolecules-11-01472-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/be44752aeade/biomolecules-11-01472-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/bae16ef9cfb6/biomolecules-11-01472-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/616ec66654cc/biomolecules-11-01472-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/dfb8ef2daf32/biomolecules-11-01472-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/3d98b413ab8b/biomolecules-11-01472-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/1349b2879a1d/biomolecules-11-01472-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/3b48221dacc8/biomolecules-11-01472-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/53f4ee740f99/biomolecules-11-01472-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/be44752aeade/biomolecules-11-01472-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/bae16ef9cfb6/biomolecules-11-01472-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/616ec66654cc/biomolecules-11-01472-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/dfb8ef2daf32/biomolecules-11-01472-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/3d98b413ab8b/biomolecules-11-01472-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/1349b2879a1d/biomolecules-11-01472-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef3e/8533447/3b48221dacc8/biomolecules-11-01472-g008.jpg

相似文献

1
AG-205 Upregulates Enzymes Involved in Cholesterol Biosynthesis and Steroidogenesis in Human Endometrial Cells Independently of PGRMC1 and Related MAPR Proteins.AG-205 可独立于 PGRMC1 和相关 MAPR 蛋白上调人子宫内膜细胞中胆固醇生物合成和类固醇生成相关的酶。
Biomolecules. 2021 Oct 6;11(10):1472. doi: 10.3390/biom11101472.
2
Spatiotemporal expression pattern of Progesterone Receptor Component (PGRMC) 1 in endometrium from patients with or without endometriosis or adenomyosis.孕激素受体膜组份 1(PGRMC)1 在子宫内膜异位症或子宫腺肌病患者子宫内膜中的时空表达模式。
J Steroid Biochem Mol Biol. 2022 Oct;223:106153. doi: 10.1016/j.jsbmb.2022.106153. Epub 2022 Jul 12.
3
Deciphering the Role of PGRMC1 During Human Decidualization Using an In Vitro Approach.利用体外方法解析 PGRMC1 在人蜕膜化中的作用。
J Clin Endocrinol Metab. 2021 Jul 13;106(8):2313-2327. doi: 10.1210/clinem/dgab303.
4
Protein complexes including PGRMC1 and actin-associated proteins are disrupted by AG-205.包括 PGRMC1 在内的蛋白复合物和与肌动蛋白相关的蛋白被 AG-205 破坏。
Biochem Biophys Res Commun. 2020 Mar 26;524(1):64-69. doi: 10.1016/j.bbrc.2019.12.108. Epub 2020 Jan 21.
5
Alterations in progesterone receptor membrane component 2 (PGRMC2) in the endometrium of macaques afflicted with advanced endometriosis.患有晚期子宫内膜异位症的猕猴子宫内膜中孕激素受体膜成分 2(PGRMC2)的改变。
Mol Hum Reprod. 2012 Jun;18(6):308-19. doi: 10.1093/molehr/gas006. Epub 2012 Feb 3.
6
Effects of estradiol, progesterone or cAMP on expression of PGRMC1 and progesterone receptor in a xenograft model of human endometrium and in endometrial cell culture.雌二醇、孕酮或 cAMP 对人子宫内膜异种移植模型和子宫内膜细胞培养中 PGRMC1 和孕激素受体表达的影响。
Steroids. 2023 Oct;198:109284. doi: 10.1016/j.steroids.2023.109284. Epub 2023 Jul 22.
7
Progesterone receptor membrane component 1 deficiency attenuates growth while promoting chemosensitivity of human endometrial xenograft tumors.孕激素受体膜组分1缺乏会减弱人子宫内膜异种移植肿瘤的生长,同时增强其化学敏感性。
Cancer Lett. 2015 Jan 28;356(2 Pt B):434-42. doi: 10.1016/j.canlet.2014.09.036. Epub 2014 Oct 7.
8
Progesterone-induced progesterone receptor membrane component 1 rise-to-decline changes are essential for decidualization.孕激素诱导的孕激素受体膜成分 1 上升-下降变化对于蜕膜化是必不可少的。
Reprod Biol Endocrinol. 2024 Feb 3;22(1):20. doi: 10.1186/s12958-024-01188-9.
9
Enhancement of cell surface expression and receptor functions of membrane progestin receptor α (mPRα) by progesterone receptor membrane component 1 (PGRMC1): evidence for a role of PGRMC1 as an adaptor protein for steroid receptors.孕激素受体膜成分 1(PGRMC1)增强细胞膜孕激素受体 α(mPRα)的表面表达和受体功能:PGRMC1 作为甾体激素受体衔接蛋白的作用证据。
Endocrinology. 2014 Mar;155(3):1107-19. doi: 10.1210/en.2013-1991. Epub 2014 Jan 1.
10
The PGRMC1 Antagonist AG-205 Inhibits Synthesis of Galactosylceramide and Sulfatide.PGRMC1 拮抗剂 AG-205 抑制半乳糖脑苷脂和硫酸脑苷脂的合成。
Cells. 2021 Dec 13;10(12):3520. doi: 10.3390/cells10123520.

引用本文的文献

1
Association Between UGT1A1 mRNA Expression and Cis-Acting Genetic Variants and Trans-Acting Transcriptional Regulators in Human Liver Samples.人肝脏样本中UGT1A1 mRNA表达与顺式作用基因变异及反式作用转录调节因子之间的关联
Genes (Basel). 2025 Aug 18;16(8):971. doi: 10.3390/genes16080971.
2
Pleiotropy of Progesterone Receptor Membrane Component 1 in Modulation of Cytochrome P450 Activity.孕激素受体膜组分1在调节细胞色素P450活性中的多效性
J Xenobiot. 2024 May 1;14(2):575-603. doi: 10.3390/jox14020034.
3
Progesterone-induced progesterone receptor membrane component 1 rise-to-decline changes are essential for decidualization.

本文引用的文献

1
Glycyrrhizin Derivatives Suppress Cancer Chemoresistance by Inhibiting Progesterone Receptor Membrane Component 1.甘草酸衍生物通过抑制孕激素受体膜成分1抑制癌症化疗耐药性。
Cancers (Basel). 2021 Jun 29;13(13):3265. doi: 10.3390/cancers13133265.
2
Deciphering the Role of PGRMC1 During Human Decidualization Using an In Vitro Approach.利用体外方法解析 PGRMC1 在人蜕膜化中的作用。
J Clin Endocrinol Metab. 2021 Jul 13;106(8):2313-2327. doi: 10.1210/clinem/dgab303.
3
Crosstalk between progesterone receptor membrane component 1 and estrogen receptor α promotes breast cancer cell proliferation.
孕激素诱导的孕激素受体膜成分 1 上升-下降变化对于蜕膜化是必不可少的。
Reprod Biol Endocrinol. 2024 Feb 3;22(1):20. doi: 10.1186/s12958-024-01188-9.
4
Inhibition of squalene epoxidase linking with PI3K/AKT signaling pathway suppresses endometrial cancer.鲨烯环氧酶与 PI3K/AKT 信号通路的抑制作用抑制子宫内膜癌。
Cancer Sci. 2023 Sep;114(9):3595-3607. doi: 10.1111/cas.15900. Epub 2023 Jul 12.
5
PGRMC1: An enigmatic heme-binding protein.PGRMC1:一种神秘的血红素结合蛋白。
Pharmacol Ther. 2023 Jan;241:108326. doi: 10.1016/j.pharmthera.2022.108326. Epub 2022 Dec 1.
6
PGRMC1 Regulates Cellular Senescence via Modulating FOXO1 Expression in Decidualizing Endometrial Stromal Cells.PGRMC1 通过调节 FOXO1 表达调控蜕膜化子宫内膜间质细胞的细胞衰老。
Biomolecules. 2022 Jul 28;12(8):1046. doi: 10.3390/biom12081046.
7
Progesterone Receptor Membrane Component (PGRMC)1 and PGRMC2 and Their Roles in Ovarian and Endometrial Cancer.孕激素受体膜成分(PGRMC)1和PGRMC2及其在卵巢癌和子宫内膜癌中的作用。
Cancers (Basel). 2021 Nov 26;13(23):5953. doi: 10.3390/cancers13235953.
8
PGRMC1 Promotes Progestin-Dependent Proliferation of Breast Cancer Cells by Binding Prohibitins Resulting in Activation of ERα Signaling.PGRMC1通过结合抑制素促进孕激素依赖的乳腺癌细胞增殖,从而导致雌激素受体α(ERα)信号通路激活。
Cancers (Basel). 2021 Nov 11;13(22):5635. doi: 10.3390/cancers13225635.
孕激素受体膜成分 1 与雌激素受体 α 之间的串扰促进乳腺癌细胞增殖。
Lab Invest. 2021 Jun;101(6):733-744. doi: 10.1038/s41374-021-00594-6. Epub 2021 Apr 26.
4
Endometriosis and Medical Therapy: From Progestogens to Progesterone Resistance to GnRH Antagonists: A Review.子宫内膜异位症与药物治疗:从孕激素到孕激素抵抗再到促性腺激素释放激素拮抗剂:综述
J Clin Med. 2021 Mar 5;10(5):1085. doi: 10.3390/jcm10051085.
5
A progesterone receptor membrane component 1 antagonist induces large vesicles independent of progesterone receptor membrane component 1 expression.孕激素受体膜成分 1 拮抗剂诱导大囊泡形成不依赖于孕激素受体膜成分 1 的表达。
Biol Chem. 2020 Aug 27;401(9):1093-1099. doi: 10.1515/hsz-2019-0417.
6
Progesterone receptor membrane component 1 promotes the growth of breast cancers by altering the phosphoproteome and augmenting EGFR/PI3K/AKT signalling.孕激素受体膜成分 1 通过改变磷酸化蛋白质组并增强 EGFR/PI3K/AKT 信号转导促进乳腺癌的生长。
Br J Cancer. 2020 Oct;123(8):1326-1335. doi: 10.1038/s41416-020-0992-6. Epub 2020 Jul 24.
7
Progesterone receptor membrane component 1 regulates lipid homeostasis and drives oncogenic signaling resulting in breast cancer progression.孕激素受体膜成分 1 调节脂质稳态并驱动致癌信号转导,导致乳腺癌进展。
Breast Cancer Res. 2020 Jul 13;22(1):75. doi: 10.1186/s13058-020-01312-8.
8
Progesterone receptor ligands for the treatment of endometriosis: the mechanisms behind therapeutic success and failure.孕激素受体配体治疗子宫内膜异位症:治疗成功和失败的背后机制。
Hum Reprod Update. 2020 Jun 18;26(4):565-585. doi: 10.1093/humupd/dmaa009.
9
Protein complexes including PGRMC1 and actin-associated proteins are disrupted by AG-205.包括 PGRMC1 在内的蛋白复合物和与肌动蛋白相关的蛋白被 AG-205 破坏。
Biochem Biophys Res Commun. 2020 Mar 26;524(1):64-69. doi: 10.1016/j.bbrc.2019.12.108. Epub 2020 Jan 21.
10
Downregulation of nuclear progestin receptor (Pgr) and subfertility in double knockouts of progestin receptor membrane component 1 (pgrmc1) and pgrmc2 in zebrafish.核孕激素受体(Pgr)下调与斑马鱼孕激素受体膜成分 1(pgrmc1)和 pgrmc2 双敲除导致的生殖力下降。
Gen Comp Endocrinol. 2020 Jan 1;285:113275. doi: 10.1016/j.ygcen.2019.113275. Epub 2019 Sep 16.