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Association between single nucleotide polymorphisms in AKT1 and the risk of prostate cancer in the Chinese Han
1Department of Urology, Institute of Urology (Laboratory of Reconstructive Urology) West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Abstract:
AKT1, also known as v-akt murine thymoma viral oncogene homolog 1, is involved in the regulation of cell-survival and anti-apoptotic activities, which may affect the pathogenesis of various cancers. However, the association between genetic variants of AKT1 and the risk of developing prostate cancer has not been investigated before. This study investigated the associations between three polymorphisms (rs1130214, rs3730358, and rs2494732) in AKT1 and the risk of development of prostate cancer in the Chinese Han population. Sequenom MassARRAY & iPLEX technology were used to genotype these polymorphisms in 493 Chinese Han patients with prostate cancer and 309 age-matched healthy individuals. Compared to the CC genotype of the rs3730358 polymorphism, the CT genotype of the same polymorphism was strongly associated with a decreased risk of prostate cancer (OR = 0.617, 95%CI = 0.390-0.976, P = 0.037). However, there was no significant difference between the allele frequency of the rs3730358 polymorphism and those of the other two polymorphisms (P > 0.05). Moreover, no significant difference was found in the haplotype analysis (P > 0.05). Our study found that the variant genotype CT of rs3730358 of AKT1 was associated with a decreased risk of prostate cancer, which suggested that this polymorphism could play an important role in the development of the disease.
Insights
Genetic variants in AKT1 may influence cancer development. A specific AKT1 gene variant (rs3730358 CT genotype) was linked to a reduced risk of prostate cancer in the Chinese Han population.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- The AKT1 gene (v-akt murine thymoma viral oncogene homolog 1) regulates cell survival and apoptosis, processes implicated in cancer pathogenesis.
- The specific role of genetic variations in AKT1 concerning prostate cancer risk remains largely unexplored.
Purpose of the Study:
- To investigate the association between three common AKT1 gene polymorphisms (rs1130214, rs3730358, and rs2494732) and the risk of developing prostate cancer.
- To analyze these associations within the Chinese Han population.
Main Methods:
- Genotyping of AKT1 polymorphisms (rs1130214, rs3730358, rs2494732) using Sequenom MassARRAY & iPLEX technology.
- Case-control study design involving 493 prostate cancer patients and 309 healthy controls from the Chinese Han population.
Main Results:
- The CT genotype of the rs3730358 polymorphism in AKT1 showed a significant association with a decreased risk of prostate cancer (OR = 0.617, P = 0.037) compared to the CC genotype.
- No significant associations were found for allele frequencies of rs3730358 or the other two polymorphisms (rs1130214, rs2494732).
- Haplotype analysis did not reveal any significant differences.
Conclusions:
- The variant genotype CT of AKT1 rs3730358 is associated with a reduced risk of prostate cancer in the Chinese Han population.
- This specific AKT1 polymorphism may play a role in prostate cancer development, warranting further investigation.
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