As technology advances, scientists are increasingly able to decipher genetic combinations and their impact on human health. A recent study has brought renewed attention to DNA damage and its potential consequences. DNA damage is generally divided into two categories: spontaneous and exogenous. Spontaneous damage refers to the natural metabolic process and caused by free radicals, while exogenous damage is mainly caused by environmental factors, such as ultraviolet rays, radiation, etc.
DNA damage is inevitable, but understanding how it affects cell function and growth is key to protecting our health.
Although DNA damage and mutations both involve changes in the genetic makeup, there are clear differences between them. DNA damage often refers to structural abnormalities, such as breaks in DNA strands or nucleotide deletions in the genome; mutations are changes in base sequence, that is, changes in genetic information. DNA damage may lead to changes in gene function, and if such changes are not repaired during replication, they may eventually evolve into mutations.
When DNA is damaged, cells initiate complex DNA damage responses (DDR) to combat these damages. The efficiency of these reaction pathways directly affects cellular health, the aging process, and the development of disease. Research shows that cells' perception and repair response to DNA damage is the basis for benign cell growth. As we age, the efficiency of these repair mechanisms often decreases, which may lead to an increased risk of health problems such as cancer.
Human cells suffer more than 100,000 DNA oxidative damages every day, mainly from metabolic processes and environmental factors. The main type of oxidative damage includes 8-oxodeoxyguanosine (8-oxo-dG), which may have a cumulative effect over time. Unrepaired damage that accumulates over time not only ages cells but can also cause cells to transform into cancer cells.
With the deepening of research, many new DNA repair pathways have been discovered, which help us understand how damage is repaired and the possible consequences of unrepaired damage.
Oxidative damage not only affects the genes themselves, but also changes their expression. Especially in nerve cells, oxidative damage to CpG sites triggers demethylation processes, thereby affecting gene stability and activity. This process plays a crucial role in the formation of memories, as a large number of genes involved in learning and memory need to be properly expressed at all times.
Long-term chronic inflammation, such as caused by viral infection or obesity, can significantly damage cellular DNA. Not only can it directly cause DNA damage, it can also further increase the risk of genetic damage by promoting increased oxidative stress. Once this damage is not repaired, it may cause cancer.
Understanding the source and impact of DNA damage not only helps us better prevent and manage potential health risks, but also gives people a deeper understanding of issues such as aging and cancer. Future research is expected to reveal more biological processes related to DNA repair and damage, thereby protecting our health. In the face of increasing DNA damage, can we develop effective strategies to protect our genes and maintain the vitality of life?