Gao Xue, Zhao Xinyu, Yang Shuhan, Liu Jianli, Liu Dan
School of Life Science, Liaoning University, 66 Chongshan Middle Road, Shenyang, 110036, People's Republic of China.
Arch Dermatol Res. 2024 Dec 14;317(1):125. doi: 10.1007/s00403-024-03607-8.
The genetic causality between cathepsin levels and autoimmune diseases (ADs) bidirectionally was investigated and the associated cancer risk was explored with Mendelian randomization. Mendelian randomization analyses were used to explore causal associations between cathepsin and 14 ADs. The final results came from a meta-analysis of two datasets to get a robust result. Furthermore, the potential carcinogenic effects of reduced cathepsin levels were explored. Sensitivity analyses were used to evaluate the robustness of the results. Based on the Mendelian randomization analysis, it was found that lower levels of specific cathepsins were associated with reduced risk of ADs. Reduced cathepsin E levels were linked to decreased susceptibility to psoriasis and a potential reduction in breast cancer risk. Reduced cathepsins G and L2 showed an inhibitory effect on psoriasis without increasing cancer risk. These results emphasized the genetic causal connection between cathepsin and ADs. Targeting cathepsins may be beneficial in treating ADs, but potential oncogenic effects must be considered to provide a basis for safer therapeutic strategies.
研究了组织蛋白酶水平与自身免疫性疾病(ADs)之间的遗传因果关系,并通过孟德尔随机化方法探讨了相关的癌症风险。采用孟德尔随机化分析来探索组织蛋白酶与14种ADs之间的因果关联。最终结果来自对两个数据集的荟萃分析,以获得可靠的结果。此外,还探讨了组织蛋白酶水平降低的潜在致癌作用。使用敏感性分析来评估结果的稳健性。基于孟德尔随机化分析,发现特定组织蛋白酶水平较低与ADs风险降低相关。组织蛋白酶E水平降低与银屑病易感性降低以及乳腺癌风险可能降低有关。组织蛋白酶G和L2水平降低对银屑病有抑制作用,且不会增加癌症风险。这些结果强调了组织蛋白酶与ADs之间的遗传因果联系。靶向组织蛋白酶可能对治疗ADs有益,但必须考虑潜在的致癌作用,以便为更安全的治疗策略提供依据。