Exploration of the diagnostic and therapeutic potential of the nucleocytoplasmic shuttling protein TMUB1 by inducing G0/G1 cell cycle arrest in ovarian cancer.

IF 1.9 Q3 ONCOLOGY
Molecular and Cellular Oncology Pub Date : 2026-03-30 eCollection Date: 2026-01-01 DOI:10.1080/23723556.2026.2650223
Jiahong Jiang, Jie Li, Shuai Tang, Liping Shu, Yanhong Chen, Jiaxian Qian, Yanzhou Wang, Yin Chen
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引用次数: 0

Abstract

Background: Ovarian cancer is one of the leading causes of gynaecologic malignancies worldwide. This study aimed to explore the diagnostic and therapeutic potential of TMUB1 in ovarian cancer.

Methods: To investigate the subcellular localization of TMUB1 under serum deprivation conditions, immunofluorescence staining was performed. The cell cycle distribution was analysed by flow cytometry. TMUB1-interacting proteins were identified through immunoprecipitation followed by mass spectrometry. Kaplan-Meier survival analysis was used to compare overall survival between patients with high and low TMUB1 expression. Stromal and immune scores for tumour tissues in TCGA were calculated to assess the tumour microenvironment.

Results: TMUB1 plays a crucial role in regulating the cell cycle by promoting entry into the G0/G1 phase. Survival analysis revealed that TMUB1 expression is positively associated with favourable prognosis in patients with ovarian cancer. Pathway enrichment analysis highlighted several tumour-related pathways, including ECM-receptor interaction, JAK-STAT signalling, p53 signalling and apoptosis. The high TMUB1 expression group presented lower stromal scores. An inverse correlation was observed between TMUB1 expression and the expression of key immune checkpoint proteins.

Conclusions: TMUB1 might participate in the regulation of the G0/G1 cell cycle arrest, and it is a potential diagnostic marker and therapeutic target for ovarian cancer.

核细胞质穿梭蛋白TMUB1在卵巢癌中诱导G0/G1细胞周期阻滞的诊断和治疗潜力的探索
背景:卵巢癌是全球妇科恶性肿瘤的主要原因之一。本研究旨在探讨TMUB1在卵巢癌中的诊断和治疗潜力。方法:采用免疫荧光染色法观察血清剥夺条件下TMUB1的亚细胞定位。流式细胞术分析细胞周期分布。通过免疫沉淀和质谱法鉴定tmub1相互作用蛋白。Kaplan-Meier生存分析比较TMUB1高表达和低表达患者的总生存率。计算TCGA肿瘤组织的基质和免疫评分,以评估肿瘤微环境。结果:TMUB1通过促进进入G0/G1期,在调节细胞周期中起关键作用。生存分析显示,TMUB1表达与卵巢癌患者的良好预后呈正相关。通路富集分析强调了几种肿瘤相关通路,包括ecm受体相互作用、JAK-STAT信号传导、p53信号传导和细胞凋亡。TMUB1高表达组间质评分较低。TMUB1的表达与关键免疫检查点蛋白的表达呈负相关。结论:TMUB1可能参与G0/G1细胞周期阻滞的调控,是卵巢癌潜在的诊断标志物和治疗靶点。
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来源期刊
Molecular and Cellular Oncology
Molecular and Cellular Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
3.20
自引率
0.00%
发文量
18
期刊介绍: For a long time, solid neoplasms have been viewed as relatively homogeneous entities composed for the most part of malignant cells. It is now clear that tumors are highly heterogeneous structures that evolve in the context of intimate interactions between cancer cells and endothelial, stromal as well as immune cells. During the past few years, experimental and clinical oncologists have witnessed several conceptual transitions of this type. Molecular and Cellular Oncology (MCO) emerges within this conceptual framework as a high-profile forum for the publication of fundamental, translational and clinical research on cancer. The scope of MCO is broad. Submissions dealing with all aspects of oncogenesis, tumor progression and response to therapy will be welcome, irrespective of whether they focus on solid or hematological neoplasms. MCO has gathered leading scientists with expertise in multiple areas of cancer research and other fields of investigation to constitute a large, interdisciplinary, Editorial Board that will ensure the quality of articles accepted for publication. MCO will publish Original Research Articles, Brief Reports, Reviews, Short Reviews, Commentaries, Author Views (auto-commentaries) and Meeting Reports dealing with all aspects of cancer research.
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