翻译后修改:杀死癌症干细胞的潜在方法
Xuedan Han1, Hai Qin2, Yu Lu1
1School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Road, Nanjing, 211198, China.
Heliyon
|August 2, 2024
概括
癌症干细胞 (CSCs) 驱动瘤复发和转移. 针对它们的翻译后蛋白质修饰 (PTM) 提供了一种有前途的新策略,用于有效治疗癌症.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 癌症研究 癌症研究
背景情况:
- 癌症转移和复发仍然是癌症治疗的重大挑战,导致高死亡率.
- 癌症干细胞 (CSCs) 因其治疗耐药性和侵入性潜力而与瘤复发和转移有关.
- CSCs具有自我更新,分化和瘤发生能力,使其根除成为关键的治疗目标.
研究的目的:
- 审查翻译后蛋白质修饰 (PTMs) 在调节CSC自我更新和复制中的作用.
- 突出PTM及其交叉通话在控制CSC行为的重要性.
- 探索PTM操纵作为一种针对CSCs的新型治疗策略.
主要方法:
- 文献综述侧重于最近对PTM和CSC的调查.
- 分析各种PTM之间的相互作用及其对CSC功能的影响.
- 对癌症干细胞生物学中PTM调节的当前知识的综合.
主要成果:
- 翻译后蛋白质修饰 (PTM) 在控制CSC自我更新和复制方面发挥着至关重要的作用.
- PTM交声显著影响CSC的行为,并有助于它们的生存和繁殖.
- 特定的PTM被确定为CSC能力的关键监管者.
结论:
- 针对PTMs代表了消除CSC种群的新和有前途的治疗途径.
- 操纵PTM提供了一种潜在的策略,以克服癌症治疗阻力.
- 对PTM的进一步研究可能会导致创新的癌症治疗方法.
更多相关视频
07:03Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
Published on: October 2, 2020
4.5K
09:24Combined Conditional Knockdown and Adapted Sphere Formation Assay to Study a Stemness-Associated Gene of Patient-derived Gastric Cancer Stem Cells
Published on: May 9, 2020
4.4K
相关概念视频
Targeted Cancer Therapies
7.5K
The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
There are several types of targeted therapies against...
7.5K
Cancer Stem Cells and Tumor Maintenance
4.9K
Early diagnosis and treatment can often cure cancer. However, even with treatment, residual cells called cancer stem cells (CSC) might remain, often causing tumor recurrence. These cancer stem cells possess the potential for self-renewal and multi-lineage differentiation and are often responsible for the therapeutic resistance displayed in most cancers.
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
4.9K
Treatment Resistant Cancers
3.3K
Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.3K
Adaptive Mechanisms in Cancer Cells
5.7K
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,...
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
5.7K
Drugs that Stabilize Microtubules
2.0K
Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
2.0K
mTOR Signaling and Cancer Progression
3.8K
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...
The mTOR pathway or the...
3.8K
