Narrative framing may increase human suboptimal choice behavior.

Under certain conditions, multiple nonhuman species have been observed engaging in choice behavior that resulted in less food earned when compared to the amount of food that was available to be earned over the course of a session. This phenomenon is particularly strong in pigeons, but has also been observed in rats and nonhuman primates. Conversely, human participants have demonstrated a propensity to choose more optimally. However, human participants do not exclusively choose the alternative associated with more reinforcement. Framing a task in a real-world narrative has been effective in improving problem-solving on other tasks such as the Wason Four-Card problem. The present study gave human participants a choice task with either abstract stimuli or with a real-world narrative. In addition, participants were given terminal stimuli that were either predictive or unpredictive of reinforcement. Thus, participants were assigned to one of four conditions: Abstract Predictive, Abstract Unpredictive, Narrative Predictive, or Narrative Unpredictive. In contrast to the improved performance on the Wason Four-Card task, the current study found no evidence that the addition of a real-world narrative improved optimal choice performance. Rather, it may have interfered with optimal choice selection in that participants who received the narrative and unpredictive terminal stimuli were at chance performance at the end of the experimental session. Conversely, participants in the Abstract Unpredictive, Abstract Predictive, and Narrative Predictive conditions all demonstrated a preference for the optimal alternative. Possible mechanisms for these findings and future directions are discussed.

Genetic variation in the TP53 pathway and bladder cancer risk. a comprehensive analysis.

INTRODUCTION: Germline variants in TP63 have been consistently associated with several tumors, including bladder cancer, indicating the importance of TP53 pathway in cancer genetic susceptibility. However, variants in other related genes, including TP53 rs1042522 (Arg72Pro), still present controversial results. We carried out an in depth assessment of associations between common germline variants in the TP53 pathway and bladder cancer risk. MATERIAL AND METHODS: We investigated 184 tagSNPs from 18 genes in 1,058 cases and 1,138 controls from the Spanish Bladder Cancer/EPICURO Study. Cases were newly-diagnosed bladder cancer patients during 1998-2001. Hospital controls were age-gender, and area matched to cases. SNPs were genotyped in blood DNA using Illumina Golden Gate and TaqMan assays. Cases were subphenotyped according to stage/grade and tumor p53 expression. We applied classical tests to assess individual SNP associations and the Least Absolute Shrinkage and Selection Operator (LASSO)-penalized logistic regression analysis to assess multiple SNPs simultaneously. RESULTS: Based on classical analyses, SNPs in BAK1 (1), IGF1R (5), P53AIP1 (1), PMAIP1 (2), SERINPB5 (3), TP63 (3), and TP73 (1) showed significant associations at p-value≤0.05. However, no evidence of association, either with overall risk or with specific disease subtypes, was observed after correction for multiple testing (p-value≥0.8). LASSO selected the SNP rs6567355 in SERPINB5 with 83% of reproducibility. This SNP provided an OR = 1.21, 95%CI 1.05-1.38, p-value = 0.006, and a corrected p-value = 0.5 when controlling for over-estimation. DISCUSSION: We found no strong evidence that common variants in the TP53 pathway are associated with bladder cancer susceptibility. Our study suggests that it is unlikely that TP53 Arg72Pro is implicated in the UCB in white Europeans. SERPINB5 and TP63 variation deserve further exploration in extended studies.