相关实验视频
Updated: Jul 24, 2025

11:46
Single Molecule Analysis of Laser Localized Psoralen Adducts
Published on: April 20, 2017
6.7K
基于天然产品 (±) - 佩哈马林A的DNA修复通路的新调节器的鉴定
Akshay S Kulkarni1, Anshurekha Dash2, Rahul D Shingare1
1Organic Chemistry Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, India; Academy of Scientific & Innovative Research (AcSIR), Ghaziabad 201002, India.
Bioorganic & medicinal chemistry
|July 1, 2023
概括
研究人员合成了天然产品 (±) - 佩哈马林A的简化类型,以对抗癌症药物耐药性. 一种demethoxy类似物通过诱导DNA损伤和抑制修复蛋白质,显示出强大的抗癌活性.
科学领域:
- 自然产品化学 自然产品化学
- 药用化学 医学化学
- 癌症生物学 癌症生物学
背景情况:
- 瘤异质性驱动药物耐药性和化学不敏感性,导致更具攻击性的癌症表型.
- 现有的破坏DNA的化疗剂往往面临由于获得的化学抵抗而受到限制.
- 自然产品 (±) - 佩哈马林A对癌细胞具有有前途的细胞毒性活性.
研究的目的:
- 设计和合成 (±) - 佩哈马林A.的新型,简化的类似物.
- 评估这些类似物对抗癌症的细胞毒性潜力.
- 为了识别与原始天然产品相比,具有增强抗癌效能的化合物.
主要方法:
- 基于 (±) - 佩哈马林 A 脚手架的简化类型库的合成.
- 合成化合物的细胞毒性活动的体外评估.
- 对其抗癌机制的脱氧类比物进行进一步调查.
主要成果:
- 鉴定了三个结构简化的类似物,其强度比 (±) - 佩哈马林A.A.更强.
- 德梅索西类比体显示出显著的抗癌潜力.
- 这种类似物作为一种强大的DNA损伤诱导剂,减少DNA修复蛋白的表达.
结论:
- (±) - 佩哈马林A的结构简化的类似物可以克服母化合物的局限性.
- 这种demethoxy类似物是进一步抗癌药物开发的有希望的候选者.
- 脱氧类比的机制涉及强大的DNA损伤诱导和干扰DNA修复途径.
相关概念视频
Nucleotide Excision Repair
3.6K
DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
3.6K
Long-patch Base Excision Repair
7.1K
Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
7.1K
Base Excision Repair
22.6K
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
The first step of...
22.6K
Negative Regulator Molecules
35.5K
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.
35.5K
Base-pairing and DNA Repair
64.8K
64.8K
Fixing Double-strand Breaks
12.7K
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
12.7K

