首页/数据集/Cancer-associated fibroblasts-secreted CXCL14-regulated LINC00092 mediates ovarian cancer progression by altering glycolysis

Cancer-associated fibroblasts-secreted CXCL14-regulated LINC00092 mediates ovarian cancer progression by altering glycolysis

ChEBI2016-06-01 更新2026-07-12 收录

卵巢癌分子机制

肿瘤代谢重编程

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-82059 数据链接链接失效反馈

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资源简介：

Cancer-associated fibroblasts-secreted CXCL14-regulated LINC00092 mediates ovarian cancer progression by altering glycolysis

应用场景：

创建时间：

2016-06-01

卵巢癌分子机制

肿瘤RNA-seq分析

The cure rate for late stage epithelial ovarian cancer (EOC) has not significantly improved over several decades. New and more effective targets and treatment modalities are urgently needed. RNA-seq a

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CXCR2-Driven Ovarian Cancer Progression Involves Upregulation of Proinflammatory Chemokines by Potentiating NF-κB Activation via EGFR-Transactivated Akt Signaling

卵巢癌分子机制

NF-κB信号通路

Ovarian cancer is an inflammation-associated malignancy with a high mortality rate. CXCR2 expressing ovarian cancers are aggressive with poorer outcomes. We therefore investigated molecular mechanisms

NIAID Data Ecosystem30

WP3303 - RAC1/PAK1/p38/MMP2 pathway - Homo sapiens

癌症信号通路

卵巢癌分子机制

Interplay of RAC1, p38 MAPK, PAK1 and MMP2 in cell signaling pathways downstream of TEK receptor activity related to tumor growth, angiogenesis, and cell proliferation. These processes are reduced in

NIAID Data Ecosystem20

Table 3_Multiomic analysis of lactylation and mitochondria-related genes in hepatocellular carcinoma identified MRPL3 as a new prognostic biomarker.xlsx

肿瘤代谢重编程

癌症预后生物标志物

BackgroundRecent research has highlighted lactate’s crucial role in epigenetic regulation, particularly by influencing histone modifications that drive the initiation and progression of hepatocellular

NIAID Data Ecosystem40

Expression data from TGF-beta-treated human ovarian fibroblasts. Homo sapiens

肿瘤微环境

卵巢癌分子机制

Advanced ovarian cancer is the most lethal gynecologic malignancy in the United States. Ovarian cancer cells are known to have diminished response to TGF-beta, but it remains unclear whether TGF-beta

NIAID Data Ecosystem20

Cancer-associated fibroblasts-secreted CXCL14-regulated LINC00092 mediates ovarian cancer progression by altering glycolysis

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