The production of neutral N∗(11052)N^*(11052) resonance with hidden beauty from π−p\pi^-p scattering

We investigate the discovery potential of the predicted neutral hidden beauty $N^*(11052)$ resonance through $\pi^- p$ scattering within an effective Lagrangian approach. Two reactions $\pi^-p\rightarrow K^-\Sigma^+$ and $\pi^-p\rightarrow \eta_bn$ are studied in this work, with nucleon pole exchange as the background. It is found that the contributions of the $N^*(11052)$ resonance give clear peak structures in the magnitude of 1 $\mu b$ near the threshold of the $N^*(11052)$ in the total cross sections. The numerical results indicate that the center of mass energy $W\simeq$ 11-11.1 GeV would be a best energy window for searching the $N^*(11052)$ resonance, where the $N^*(11052)$ signal can be easily distinguished from the background. The COMPASS experiment at CERN's Super Proton Synchrotron (SPS) with pion beam of $\simeq$ 280 GeV will be an ideal platform for searching the super-heavy resonance with hidden beauty, which is hopeful to test the theoretical results

The association of XRCC1 gene single nucleotide polymorphisms with response to neoadjuvant chemotherapy in locally advanced cervical carcinoma

<p>Abstract</p> <p>Background</p> <p>Platinum-based neoadjuvant chemotherapy (NAC) is new therapeutic strategy for locally advanced cervical carcinoma, but the variables used to predict NAC response are still infrequently reported. The aim of our study was to investigate the association between <it>XRCC1 </it>gene single nucleotide polymorphisms (SNPs) and NAC response.</p> <p>Methods</p> <p>Seventy patients with locally advanced cervical carcinoma who underwent NAC were collected. SNPs of <it>XRCC1 </it>(at codon 194 and 399) and XRCC1 protein expression were detected. The association of <it>XRCC1 </it>gene SNPs and protein expression with NAC response were analyzed.</p> <p>Results</p> <p>Response to NAC was not statistically significant in three genotypes, Arg/Arg, Arg/Trp, Trp/Trp of <it>XRCC1 </it>at codon 194(X²= 1.243, P = 0.07), while responses were significantly different in genotypes Arg/Arg, Arg/Gln, Gln/Gln of <it>XRCC1 </it>at codon 399 (X²= 2.283, P = 0.020). The risk of failure to chemotherapy in the patients with a Gln allele(Arg/Gln+Gln/Gln) was significantly greater than that with Arg/Arg(OR = 3.254, 95%CI 1.708 ~ 14.951). The expression level of XRCC1 protein was significantly associated with response to NAC. Moreover, the genotype with the Gln allele(Arg/Gln+Gln/Gln) at codon 399, but not codon at 194, presented a significantly higher level of XRCC1 protein expression than that with Arg/Arg genotype (F = 2.699, p = 0.009).</p> <p>Conclusion</p> <p>SNP of <it>XRCC1 </it>gene at codon 399 influences the response of cervical carcinoma to platinum-based NAC. This is probably due to changes in expression of XRCC1 protein, affecting response to chemotherapy.</p

The correlation between the severity of radiotherapy-induced glossitis and endothelial cell injury in local tissues in a rat model

Objectives: To explore the correlation between the severity of radiotherapy-induced glossitis (RTG) and endothelial cell injury in local tissues in a rat model. Study Design: The RTG animal model was designed and used by our team. The Oral mucositis index(OMI) was documented daily. Immunohistochemistry (IHC) Staining of CD34 was utilized to identify endothelial cells in the RTG tissues. Apoptosis of endothelial cells in local lesions due to RTG was detected by the TUNEL assay. The dynamic relationship between the OMI and apoptotic endothelial cells was statistically analyzed by time. Results and Conclusions: The injury and apoptosis of endothelial cells were observed 3 day post-irradiation. The vascular lumens of the post-irradiation tongue lesions were irregular; thrombosis formation in the center of the lumens, unsmooth lumen walls and vasodilated vessels were observed. Also, endothelial cells detached from the basal membrane and were found in the lumens. The percentages (%) of apoptotic endothelial cells were 78.3±0.31 (5 day); 89.3±0.83 (8 day); 83.5±0.41 (14 day); 69.3±0.57 (21 day); and 47.3±0.59 (28 day). The OMI was correlated with the percentage of apoptotic endothelial cells (R=0.67, P=0.034). Summary, endothelial cell injury was correlated with the pathogenic condition of RTG. © Medicina Oral S. L