在口腔癌前和癌症阶段比较长度和端粒表达
Fahad Mansoor Samadi1, Shaista Suhail1, Manjari Sonam2
1Department of Oral Pathology and Microbiology, King George Medical University, Lucknow, India.
Iranian journal of pathology
|August 9, 2024
概括
在口腔癌前病变和口腔状细胞癌 (OSCC) 之间,端粒长度和端粒酶活性显著不同. 这一发现为早期OSCC检测和预后提供了潜在的生物标志物.
科学领域:
- 遗传学 是一个遗传学.
- 在瘤学瘤学.
- 分子生物学分子生物学
背景情况:
- 端粒是染色体末端的G丰富的核酸重复,对染色体稳定性至关重要.
- 端粒长度和端粒酶活性与癌症的发展和进展有关.
研究的目的:
- 在血液,唾液和组织样本中调查端粒长度和端粒酶活性之间的差异.
- 为了在口腔癌前和癌症病变的不同阶段比较这些标志物.
主要方法:
- 从患有口腔癌前和癌症病变的患者收集血液,唾液和组织样本.
- 进行DNA提取并使用TRAP测试来测量端粒长度和端粒酶表达.
主要成果:
- 在口腔状细胞癌 (OSCC) 患者和癌前患者 (P=0.0000) 之间,端粒酶活性 (TA) 水平有显著的差异.
- 在OSCC和癌前样本之间观察到TA水平的统计学上显著差异.
结论:
- 测量端粒酶活性对于了解口腔癌的行为至关重要.
- 提升的端粒酶表达和端粒长度有助于OSCC的进展.
- 这项研究引入了用于早期OSCC检测和预后的潜在诊断生物标志物.
相关概念视频
Replicative Cell Senescence
3.6K
Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds...
3.6K
Telomeres and Telomerase
23.2K
In eukaryotic DNA replication, a single-stranded DNA fragment remains at the end of a chromosome after the removal of the final primer. This section of DNA cannot be replicated in the same manner as the rest of the strand because there is no 3’ end to which the newly synthesized DNA can attach. This non-replicated fragment results in gradual loss of the chromosomal DNA during each cell duplication. Additionally, it can induce a DNA damage response by enzymes that recognize single-stranded...
23.2K
Tumor Progression
6.3K
Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
6.3K
lncRNA - Long Non-coding RNAs
8.5K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
8.5K
Non-LTR Retrotransposons
11.4K
As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
11.4K


