Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Adaptive Mechanisms in Cancer Cells02:53

Adaptive Mechanisms in Cancer Cells

7.2K
Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
7.2K
Abnormal Proliferation02:23

Abnormal Proliferation

5.3K
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...
5.3K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

4.9K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
4.9K
The Tumor Microenvironment02:17

The Tumor Microenvironment

7.9K
Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
7.9K
Overview of Protein Metabolism01:21

Overview of Protein Metabolism

4.1K
Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
4.1K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Aneuploidy selects for the acquisition of driver genes in breast cancer.

Nature·2026
Same author

Isolation of Bacteria and Fungi from Human Pancreatic Tumors and Duodenum.

Gut microbes·2026
Same author

Choline-dependent methionine metabolism supports leukemia progression.

Communications biology·2026
Same author

GABA signaling activation drives glioblastoma progression in female mice through myeloid-derived suppressor cells.

Nature cancer·2026
Same author

Redox imbalance dictates dependence on GOT1 versus GOT2 for rod photoreceptor health during aging and stress.

Redox biology·2026
Same author

Analytics Methodology to Quantify MRI Exam Utilization.

Journal of imaging informatics in medicine·2026

相关实验视频

Updated: Feb 17, 2026

The Colon-26 Carcinoma Tumor-bearing Mouse as a Model for the Study of Cancer Cachexia
08:55

The Colon-26 Carcinoma Tumor-bearing Mouse as a Model for the Study of Cancer Cachexia

Published on: November 30, 2016

17.2K

来自瘤的多氨基酸在癌症中启动脂肪消耗.

Matias Fabregat, Rachel J Fenske, Julia K Hansen

    bioRxiv : the preprint server for biology
    |February 16, 2026
    PubMed
    概括

    癌症相关的 (CC) 涉及到由瘤衍生的多氨酸驱动的早期脂肪浪费. 这种聚胺依赖的交叉干涉促进了脂解,为癌症患者的早期检测和干预提供了潜在的生物标志物.

    更多相关视频

    Evaluation of Amino Acid Consumption in Cultured Bone Cells and Isolated Bone Shafts
    06:32

    Evaluation of Amino Acid Consumption in Cultured Bone Cells and Isolated Bone Shafts

    Published on: April 13, 2022

    2.1K
    Transfer of Manipulated Tumor-associated Neutrophils into Tumor-Bearing Mice to Study their Angiogenic Potential In Vivo
    08:19

    Transfer of Manipulated Tumor-associated Neutrophils into Tumor-Bearing Mice to Study their Angiogenic Potential In Vivo

    Published on: July 20, 2019

    6.5K

    相关实验视频

    Last Updated: Feb 17, 2026

    The Colon-26 Carcinoma Tumor-bearing Mouse as a Model for the Study of Cancer Cachexia
    08:55

    The Colon-26 Carcinoma Tumor-bearing Mouse as a Model for the Study of Cancer Cachexia

    Published on: November 30, 2016

    17.2K
    Evaluation of Amino Acid Consumption in Cultured Bone Cells and Isolated Bone Shafts
    06:32

    Evaluation of Amino Acid Consumption in Cultured Bone Cells and Isolated Bone Shafts

    Published on: April 13, 2022

    2.1K
    Transfer of Manipulated Tumor-associated Neutrophils into Tumor-Bearing Mice to Study their Angiogenic Potential In Vivo
    08:19

    Transfer of Manipulated Tumor-associated Neutrophils into Tumor-Bearing Mice to Study their Angiogenic Potential In Vivo

    Published on: July 20, 2019

    6.5K

    科学领域:

    • 在瘤学瘤学.
    • 代谢障碍 代谢障碍 代谢障碍
    • 分子生物学分子生物学

    背景情况:

    • 癌症相关的 (CC) 是一种致命的代谢状况,早期的分子驱动因素尚不清楚.
    • CC涉及逐渐减少脂肪和肌肉质量,显著影响患者的结果.

    研究的目的:

    • 为了识别癌症相关缓解症的早期分子驱动因素.
    • 为了研究多氨酸在瘤-脂肪交叉的作用,在前-cachexia.

    主要方法:

    • 利用临床前模型研究聚胺积累及其对脂肪细胞的影响.
    • 分析了细胞外囊泡的癌症衍生的聚胺丰富.
    • 在新诊断的胰腺癌患者中使用自动CT成像来评估脂肪组织密度.
    • 与临床数据和患者存活率相关联的聚胺水平.

    主要成果:

    • 确定了一种聚胺依赖的瘤-脂肪交叉触发脂肪细胞脂解和脂肪消耗在前形阶段.
    • 证明癌症衍生的聚氨酸,富含细胞外囊泡,通过eIF5A低化促进脂质调动,独立于上腺体信号传递.
    • 观察到,在临床前模型中聚胺的积累与早期的脂肪损失和循环脂肪酸的增加有关.
    • 发现胰腺癌患者的脂肪密度增加与循环中的聚胺水平相关,并预测生存率差.

    结论:

    • 聚胺代谢是早期癌症相关的缓解症的机械驱动因素.
    • 循环中的聚胺水平作为早期缓解症检测的候选生物标志物.
    • 这些发现为开发早期检测策略和针对癌症缓解症的有针对性的干预提供了框架.