Comprehensive analysis of the effect of rs2295080 and rs2536 polymorphisms within the mTOR gene on cancer risk.

There is still no conclusion on the potential effect of the rs2295080 and rs2536 polymorphisms of mTOR (mammalian target of rapamycin) gene on different cancers. Herein, we performed a comprehensive assessment using pooled analysis, FPRP (false-positive report probability), TSA (trial sequential analysis), and eQTL (expression quantitative trait loci) analysis. Eighteen high-quality articles from China were enrolled. The pooled analysis of rs2295080 with 9502 cases and 10,965 controls showed a decreased risk of urinary system tumors and specific prostate cancers [TG vs. TT, TG+GG vs. TT and G vs. T; P<0.05, OR (odds ratio) <1]. FPRP and TSA data further confirmed these results. There was an increased risk of leukemia [G vs. T, GG vs. TT, and GG vs. TT+TG genotypes; P<0.05, OR>1]. The eQTL data showed a potential correlation between the rs2295080 and mTOR expression in whole blood samples. Nevertheless, FPRP and TSA data suggested that more evidence is required to confirm the potential role of rs2295080 in leukemia risk. The pooled analysis of rs2536 (6653 cases and 7025 controls) showed a significant association in the subgroup of "population-based" control source via the allele, heterozygote, dominant, and carrier comparisons (P<0.05, OR>1). In conclusion, the TG genotype of mTOR rs2295080 may be linked to reduced susceptibility to urinary system tumors or specific prostate cancers in Chinese patients. The currently data do not strongly support a role of rs2295080 in leukemia susceptibility. Large sample sizes are needed to confirm the potential role of rs2536 in more types of cancer.

[Multi-scale spatial variability of soil salinity in typical fields of the Yellow River Delta in summer]. / é»„æ²³ä¸‰è§’æ´²å¤å­£å ¸åž‹ç”°å—åœŸå£¤ç›åˆ†çš„å¤šå°ºåº¦ç©ºé—´å˜å¼‚.

Soil salinization severely hinders the development of agricultural economy in the Yellow River Delta. Clarifying the spatial variability of soil salinity at multiple scales in the field is of great significance for the improvement and utilization of saline soils and agricultural production. In this study, by dividing the three dimensions of field, plot and ridge, we collceted 152 sets of conducti-vity data through field survey sampling in a summer maize field in Kenli County of the Yellow River delta. The methods of classic statistics, geostatistics and Kriging interpolation were used to analyze the spatial variability and scale effects of multi-scale soil salt in the field. The results showed that soil in this area was moderately salinized, with the extent of soil salinity moderately varying at three scales. From the field, plot to the ridge scale, with the decreases of sampling scale, the variability of soil salinity increased and the standard deviation increased. The ridge and plot scales showed strong spatial correlation. The optimal model was Gaussian model, which was mainly affected by structural factors. The field scale was of medium spatial correlation, with exponential model as the optimal one, which was influenced by both random factors and structural factors. The spatial distribution characteristics of soil salinity at different scales were significantly different. The spatial chara-cteristics at small scale were masked at large scale, showing obvious scale effect. The distribution of soil salinity at the micro-ridge scale between ridges had obvious variation. Soil salt content gradually decreased with the micro-topography from high to low, while vegetation coverage changed from sparse to dense.

Comprehensive Analysis of the Association Between the rs1138272 Polymorphism of the GSTP1 Gene and Cancer Susceptibility.

Background: We obtained conflicting results regarding the relationship between the genetic role of the rs1138272 C/T polymorphism of the GSTP1 (Glutathione S-Transferase pi) gene and the risk of various cancers. Methods: Using the presently available data, a meta-analysis was conducted to comprehensively evaluate the genetic relationship between the GSTP1 rs1138272 polymorphism and cancer susceptibility. Results: A total of 43 studies including 15,688 cases and 17,143 controls were recruited into our quantitative synthesis. In the overall population, we observed an increased risk of overall cancer cases, compared with unrelated controls, in the genetic models of allele T vs. allele C (P-association = 0.007, OR = 1.17), carrier T vs. carrier C (P-association = 0.035, OR = 1.11), TT vs. CC (P-association = 0.002, OR = 1.45), TT vs. CC+CT (P-association = 0.009, OR = 1.42), and CT+TT vs. CC (P-association = 0.027, OR = 1.13). We detected similar positive results within the Asian population. Additionally, there was a significant increase in the incidence of cancer for Africans under all genetic models (all P-association < 0.05, OR > 1). When targeting the Caucasian population, we detected a positive association with the TT vs. CC and TT vs. CC+CT models in the "Colorectal cancer" (P-association < 0.05, OR < 1) and "Head and neck cancer" (P-association < 0.05, OR > 1) subgroups. For the "Lung cancer" subgroup, we observed a slightly increased risk in Caucasians under the models of allele T vs. allele C, carrier T vs. carrier C, CT vs. CC, and CT+TT vs. CC (P-association < 0.05, OR > 1). Conclusion: The TT genotype of the GSTP1 rs1138272 polymorphism is likely related to the susceptibility to overall cancer in the Asian and African populations and, specifically, "Colorectal" and "Head and neck" cancers in the Caucasian population. In addition, the CT genotype of the GSTP1 rs1138272 polymorphism may be linked to the risk of lung cancer in Caucasians. Additional evidence is required to confirm this conclusion.