• 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

一种新型子宫平滑肌瘤亚型表现出NRF2激活以及与Cullin 3-RING E3连接酶的Neddylation相关基因的突变。

A novel uterine leiomyoma subtype exhibits NRF2 activation and mutations in genes associated with neddylation of the Cullin 3-RING E3 ligase.

作者信息

Mehine Miika, Ahvenainen Terhi, Khamaiseh Sara, Härkönen Jouni, Reinikka Siiri, Heikkinen Tuomas, Äyräväinen Anna, Pakarinen Päivi, Härkki Päivi, Pasanen Annukka, Levonen Anna-Liisa, Bützow Ralf, Vahteristo Pia

机构信息

Applied Tumor Genomics Research Program, University of Helsinki, Helsinki, Finland.

Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.

出版信息

Oncogenesis. 2022 Sep 7;11(1):52. doi: 10.1038/s41389-022-00425-3.

DOI:10.1038/s41389-022-00425-3
PMID:36068196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9448808/
Abstract

Uterine leiomyomas, or fibroids, are the most common tumors in women of reproductive age. Uterine leiomyomas can be classified into at least three main molecular subtypes according to mutations affecting MED12, HMGA2, or FH. FH-deficient leiomyomas are characterized by activation of the NRF2 pathway, including upregulation of the NRF2 target gene AKR1B10. Here, we have identified a novel leiomyoma subtype showing AKR1B10 expression but no alterations in FH or other known driver genes. Whole-exome and whole-genome sequencing revealed biallelic mutations in key genes involved in neddylation of the Cullin 3-RING E3 ligase, including UBE2M, NEDD8, CUL3, and NAE1. 3'RNA sequencing confirmed a distinct molecular subtype with activation of the NRF2 pathway. Most tumors displayed cellular histopathology, perivascular hypercellularity, and characteristics typically seen in FH-deficient leiomyomas. These results suggest a novel leiomyoma subtype that is characterized by distinct morphological features, genetic alterations disrupting neddylation of the Cullin 3-RING E3 ligase, and oncogenic NRF2 activation. They also present defective neddylation as a novel mechanism leading to aberrant NRF2 signaling. Molecular characterization of uterine leiomyomas provides novel opportunities for targeted treatment options.

摘要

子宫平滑肌瘤,即纤维瘤,是育龄女性中最常见的肿瘤。根据影响MED12、HMGA2或FH的突变,子宫平滑肌瘤可分为至少三种主要的分子亚型。FH缺陷型平滑肌瘤的特征是NRF2通路激活,包括NRF2靶基因AKR1B10的上调。在此,我们鉴定出一种新的平滑肌瘤亚型,其显示AKR1B10表达,但FH或其他已知驱动基因无改变。全外显子组和全基因组测序揭示了参与Cullin 3-RING E3连接酶Neddylation的关键基因的双等位基因突变,包括UBE2M、NEDD8、CUL3和NAE1。3'RNA测序证实了一种具有NRF2通路激活的独特分子亚型。大多数肿瘤表现出细胞组织病理学、血管周围细胞增多,以及FH缺陷型平滑肌瘤中常见的特征。这些结果提示了一种新的平滑肌瘤亚型,其特征为独特的形态学特征、破坏Cullin 3-RING E3连接酶Neddylation的基因改变,以及致癌性NRF2激活。它们还提出Neddylation缺陷是导致异常NRF2信号传导的一种新机制。子宫平滑肌瘤的分子特征为靶向治疗选择提供了新的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/9448808/d2650529aed3/41389_2022_425_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/9448808/3ca2579c2f3f/41389_2022_425_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/9448808/a68400a680cd/41389_2022_425_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/9448808/32e6a54a10af/41389_2022_425_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/9448808/d2650529aed3/41389_2022_425_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/9448808/3ca2579c2f3f/41389_2022_425_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/9448808/a68400a680cd/41389_2022_425_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/9448808/32e6a54a10af/41389_2022_425_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/9448808/d2650529aed3/41389_2022_425_Fig4_HTML.jpg

相似文献

1
A novel uterine leiomyoma subtype exhibits NRF2 activation and mutations in genes associated with neddylation of the Cullin 3-RING E3 ligase.一种新型子宫平滑肌瘤亚型表现出NRF2激活以及与Cullin 3-RING E3连接酶的Neddylation相关基因的突变。
Oncogenesis. 2022 Sep 7;11(1):52. doi: 10.1038/s41389-022-00425-3.
2
3'RNA and whole-genome sequencing of archival uterine leiomyomas reveal a tumor subtype with chromosomal rearrangements affecting either HMGA2, HMGA1, or PLAG1.对存档的子宫平滑肌瘤进行 3'RNA 和全基因组测序,揭示了一种具有染色体重排的肿瘤亚型,影响 HMGA2、HMGA1 或 PLAG1。
Genes Chromosomes Cancer. 2023 Jan;62(1):27-38. doi: 10.1002/gcc.23088. Epub 2022 Aug 1.
3
3'RNA Sequencing Accurately Classifies Formalin-Fixed Paraffin-Embedded Uterine Leiomyomas.3'RNA测序可准确分类福尔马林固定石蜡包埋的子宫平滑肌瘤。
Cancers (Basel). 2020 Dec 19;12(12):3839. doi: 10.3390/cancers12123839.
4
Integrated data analysis reveals uterine leiomyoma subtypes with distinct driver pathways and biomarkers.综合数据分析揭示了具有不同驱动途径和生物标志物的子宫平滑肌瘤亚型。
Proc Natl Acad Sci U S A. 2016 Feb 2;113(5):1315-20. doi: 10.1073/pnas.1518752113. Epub 2016 Jan 19.
5
Characterization of MED12, HMGA2, and FH alterations reveals molecular variability in uterine smooth muscle tumors.MED12、HMGA2和FH改变的特征揭示了子宫平滑肌肿瘤中的分子变异性。
Mol Cancer. 2017 Jun 7;16(1):101. doi: 10.1186/s12943-017-0672-1.
6
Systematic molecular and clinical analysis of uterine leiomyomas from fertile-aged women undergoing myomectomy.对行子宫肌瘤剔除术的生育期妇女的子宫平滑肌瘤进行系统的分子和临床分析。
Hum Reprod. 2020 Oct 1;35(10):2237-2244. doi: 10.1093/humrep/deaa187.
7
MED12 exon 2 mutations in histopathological uterine leiomyoma variants.MED12 外显子 2 突变与组织病理学子宫平滑肌瘤变异。
Eur J Hum Genet. 2013 Nov;21(11):1300-3. doi: 10.1038/ejhg.2013.33. Epub 2013 Feb 27.
8
mutations and fumarate hydratase inactivation in uterine adenomyomas.子宫腺肌瘤中的突变与富马酸水合酶失活
Hum Reprod Open. 2018 Nov 17;2018(4):hoy020. doi: 10.1093/hropen/hoy020. eCollection 2018.
9
Genomics of uterine leiomyomas: insights from high-throughput sequencing.子宫平滑肌瘤的基因组学:高通量测序的研究进展。
Fertil Steril. 2014 Sep;102(3):621-9. doi: 10.1016/j.fertnstert.2014.06.050. Epub 2014 Aug 5.
10
Inherited mutations affecting the SRCAP complex are central in moderate-penetrance predisposition to uterine leiomyomas.影响 SRCAP 复合物的遗传突变是中等外显率子宫平滑肌瘤易感性的核心因素。
Am J Hum Genet. 2023 Mar 2;110(3):460-474. doi: 10.1016/j.ajhg.2023.01.009. Epub 2023 Feb 10.

引用本文的文献

1
Chromatin state origins of uterine leiomyoma.子宫平滑肌瘤的染色质状态起源
Nat Commun. 2025 May 8;16(1):4307. doi: 10.1038/s41467-025-59646-w.
2
UTERINE FIBROIDS.子宫肌瘤
Physiol Rev. 2025 Oct 1;105(4):1947-1988. doi: 10.1152/physrev.00010.2024. Epub 2025 Apr 11.
3
Health position paper and redox perspectives - Bench to bedside transition for pharmacological regulation of NRF2 in noncommunicable diseases.健康立场文件与氧化还原观点——非传染性疾病中NRF2药理调节从 bench 到床边的转化

本文引用的文献

1
Comparison of 2SC, AKR1B10, and FH Antibodies as Potential Biomarkers for FH-deficient Uterine Leiomyomas.2SC、AKR1B10 和 FH 抗体在 FH 缺乏型子宫平滑肌瘤中作为潜在生物标志物的比较。
Am J Surg Pathol. 2022 Apr 1;46(4):537-546. doi: 10.1097/PAS.0000000000001826.
2
Deficient H2A.Z deposition is associated with genesis of uterine leiomyoma.H2A.Z 沉积不足与子宫肌瘤的发生有关。
Nature. 2021 Aug;596(7872):398-403. doi: 10.1038/s41586-021-03747-1. Epub 2021 Aug 4.
3
Selective inhibition of cullin 3 neddylation through covalent targeting DCN1 protects mice from acetaminophen-induced liver toxicity.
Redox Biol. 2025 Apr;81:103569. doi: 10.1016/j.redox.2025.103569. Epub 2025 Mar 3.
4
Activation of FGFR genes by genetic and epigenetic alterations in uterine leiomyomas.子宫平滑肌瘤中基因和表观遗传改变导致FGFR基因激活。
BJC Rep. 2025 Feb 27;3(1):9. doi: 10.1038/s44276-025-00127-4.
5
Detection of exon2-MED12 mutations in uterine leiomyomas from Syrian patients.叙利亚患者子宫平滑肌瘤中外显子2-MED12突变的检测
Sci Rep. 2025 Jan 2;15(1):452. doi: 10.1038/s41598-024-84439-4.
6
The Double-Edged Effects of MLN4924: Rethinking Anti-Cancer Drugs Targeting the Neddylation Pathway.MLN4924 的双刃剑效应:重新思考针对泛素化途径的抗癌药物。
Biomolecules. 2024 Jun 21;14(7):738. doi: 10.3390/biom14070738.
7
Pivotal Role of Ubiquitin Carboxyl-Terminal Hydrolase L1 (UCHL1) in Uterine Leiomyoma.泛素羧基末端水解酶 L1(UCHL1)在子宫肌瘤中的关键作用。
Biomolecules. 2023 Jan 18;13(2):193. doi: 10.3390/biom13020193.
8
Inherited mutations affecting the SRCAP complex are central in moderate-penetrance predisposition to uterine leiomyomas.影响 SRCAP 复合物的遗传突变是中等外显率子宫平滑肌瘤易感性的核心因素。
Am J Hum Genet. 2023 Mar 2;110(3):460-474. doi: 10.1016/j.ajhg.2023.01.009. Epub 2023 Feb 10.
通过共价靶向 DCN1 选择性抑制 Cullin 3 泛素化来保护小鼠免受对乙酰氨基酚引起的肝毒性。
Nat Commun. 2021 May 11;12(1):2621. doi: 10.1038/s41467-021-22924-4.
4
The Role of NRF2/KEAP1 Signaling Pathway in Cancer Metabolism.NRF2/KEAP1 信号通路在癌症代谢中的作用。
Int J Mol Sci. 2021 Apr 22;22(9):4376. doi: 10.3390/ijms22094376.
5
Therapeutic Targeting of the NRF2 Signaling Pathway in Cancer.癌症中 NRF2 信号通路的治疗靶向。
Molecules. 2021 Mar 5;26(5):1417. doi: 10.3390/molecules26051417.
6
3'RNA Sequencing Accurately Classifies Formalin-Fixed Paraffin-Embedded Uterine Leiomyomas.3'RNA测序可准确分类福尔马林固定石蜡包埋的子宫平滑肌瘤。
Cancers (Basel). 2020 Dec 19;12(12):3839. doi: 10.3390/cancers12123839.
7
WikiPathways: connecting communities.维基路径:连接社区。
Nucleic Acids Res. 2021 Jan 8;49(D1):D613-D621. doi: 10.1093/nar/gkaa1024.
8
NEDD8 and ubiquitin ligation by cullin-RING E3 ligases.Cullin-RING E3 连接酶介导的 NEDD8 和泛素连接。
Curr Opin Struct Biol. 2021 Apr;67:101-109. doi: 10.1016/j.sbi.2020.10.007. Epub 2020 Nov 5.
9
-Null Leiomyosarcoma: A Novel, Genomically Distinct Class of /-Wild-Type Tumor With Frequent Genomic Alterations and 1p/19q-Codeletion.- 无特征性平滑肌肉瘤:一种新型的、基因组特征独特的野生型肿瘤,伴有频繁的基因组改变和1p/19q缺失。
JCO Precis Oncol. 2020 Sep 1;4. doi: 10.1200/PO.20.00040. eCollection 2020.
10
Systematic molecular and clinical analysis of uterine leiomyomas from fertile-aged women undergoing myomectomy.对行子宫肌瘤剔除术的生育期妇女的子宫平滑肌瘤进行系统的分子和临床分析。
Hum Reprod. 2020 Oct 1;35(10):2237-2244. doi: 10.1093/humrep/deaa187.