miR-195-5p抑制KRT80表达,诱导结肠癌中的细胞循环停止
Emanuele Piccinno1, Viviana Scalavino1, Nicoletta Labarile1
1National Institute of Gastroenterology S. De Bellis, IRCCS Research Hospital, Via Turi 27, 70013 Castellana Grotte, Italy.
Cancers
|July 12, 2025
概括
微RNA-195-5p通过降低氨酸80 (KRT80) 表达的调节来抑制结直肠癌 (CRC) 的生长. 这种相互作用阻止了癌症细胞周期的进展,为CRC提供了潜在的治疗点.
科学领域:
- 分子生物学分子生物学
- 在瘤学瘤学.
- 基因调节 基因调节
背景情况:
- 质蛋白对于上皮细胞骨架完整性和细胞功能至关重要.
- 氨酸80 (KRT80) 被认为是各种癌症的致癌驱动因素.
- 对于KRT80在结直肠癌 (CRC) 发病过程中的作用尚不清楚.
研究的目的:
- 研究结直肠癌中miR-195-5p和KRT80之间的调节关系.
- 阐明这种相互作用对CRC细胞增殖和瘤生长的功能影响.
主要方法:
- 生物信息分析确定了KRT80 3'-UTR.中的miR-195-5p结合位.
- 在CRC组织和细胞系中通过mRNA和蛋白质分析验证了KRT80的表达.
- 功能性测试 (模仿传染,siRNA沉默,体内研究) 评估了miR-195-5p对KRT80和CRC进展的影响.
主要成果:
- miR-195-5p显著降低了CRC细胞系和小鼠模型中的KRT80表达.
- 低调 KRT80 诱导 G1 阶段细胞循环停止和减少 G2/M 种群.
- miR-195-5p通过抑制CRC生长表现出抑制瘤的活性.
结论:
- 在结直肠癌中,miR-195-5p作为KRT80的负调节剂.
- 这个miR-195-5p/KRT80轴代表了一种具有治疗CRC治疗潜力的新型分子机制.
更多相关视频
06:00Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
Published on: May 14, 2016
11.1K
09:45An In Vitro Protocol for Evaluating MicroRNA Levels, Functions, and Associated Target Genes in Tumor Cells
Published on: May 21, 2019
8.5K
相关概念视频
Abnormal Proliferation
4.6K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.6K
Inhibition of Cdk Activity
4.9K
The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
4.9K
Negative Regulator Molecules
36.1K
Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
36.1K
The Retinoblastoma Gene
4.2K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.2K
Mitogens and the Cell Cycle
6.9K
Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
6.9K
MicroRNAs
3.1K
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
3.1K
