A pan-cancer analysis of the clinical and genetic portraits of somatostatin receptor expressing tumor as a potential target of peptide receptor imaging and therapy

Abstract Purpose Although somatostatin receptor (SST) is a promising theranostic target and is widely expressed in tumors of various organs, the indication for therapies targeting SST is limited to typical gastroenteropancreatic neuroendocrine tumors (NETs). Thus, broadening the scope of the current clinical application of peptide receptor radiotherapy (PRRT) can be supported by a better understanding of the landscape of SST-expressing tumors. Methods SST expression levels were assessed in data from The Cancer Genome Atlas across 10,701 subjects representing 32 cancer types. As the major target of PRRT is SST subtype 2 (SST2), correlation analyses between the pan-cancer profiles, including clinical and genetic features, and SST2 level were conducted. The median SST2 expression level of pheochromocytoma and paraganglioma (PCPG) samples was used as the threshold to define high-SST2 tumors. The prognostic value of SST2 in each cancer subtype was evaluated by using Cox proportional regression analysis. Results We constructed a resource of SST expression patterns associated with clinicopathologic features and genomic alterations. It provides an interactive tool to analyze SST expression patterns in various cancer types. As a result, eight of the 31 cancer subtypes other than PCPG had more than 5% of tumors with high-SST2 expression. Low-grade glioma (LGG) showed the highest proportion of high-SST2 tumors, followed by breast invasive carcinoma (BRCA). LGG showed different SST2 levels according to tumor grade and histology. IDH1 mutation was significantly associated with high-SST2 status. In BRCA, the SST2 level was different according to the hormone receptor status. High-SST2 status was significantly associated with good prognosis in LGG patients. High-SST2 status showed a trend for association with poor prognosis in triple-negative breast cancer subjects. Conclusion A broad range of SST2 expression was observed across diverse cancer subtypes. The SST2 expression level showed a significant association with genomic and clinical aspects across cancers, especially in LGG and BRCA. These findings extend our knowledge base to diversify the indications for PRRT as well as SST imaging

Entropic force approach to noncommutative Schwarzschild black holes signals a failure of current physical ideas

Recently, a new perspective of gravitational-thermodynamic duality as an entropic force arising from alterations in the information connected to the positions of material bodies is found. In this paper, we generalize some aspects of this model in the presence of noncommutative Schwarzschild black hole by applying the method of coordinate coherent states describing smeared structures. We implement two different distributions: (a) Gaussian and (b) Lorentzian. Both mass distributions prepare the similar quantitative aspects for the entropic force. Our study shows, the entropic force on the smallest fundamental unit of a holographic screen with radius $r_0$ vanishes. As a result, black hole remnants are unconditionally inert even gravitational interactions do not exist therein. So, a distinction between gravitational and inertial mass in the size of black hole remnant is observed, i.e. the failure of the principle of equivalence. In addition, if one considers the screen radius to be less than the radius of the smallest holographic surface at the Planckian regime, then one encounters some unusual dynamical features leading to gravitational repulsive force and negative energy. On the other hand, the significant distinction between the two distributions is conceived to occur around $r_0$, and that is worth of mentioning: at this regime either our analysis is not the proper one, or non-extensive statistics should be employed.Comment: 15 pages, 2 figures, new references added, minor revision, Title changed, to appear in EPJ Plu

Boosting n-type doping levels of Ge with co-doping by integrating plasma-assisted atomic layer deposition and flash annealing process

To achieve a high concentration of dopants over 1 × 1020 cm-3 on germanium (Ge), co-doping with phosphorus (P) and antimony (Sb) by plasma assisted atomic layer deposition (PALD) and a subsequent annealing process [rapid thermal annealing process (RTP) or flash lamp annealing process (FLP)] are proposed and investigated. We found that the PALD stacked co-doping (POx /SiOy and Sb2O5 ) films were uniformly deposited. Using the conventional RTP method led to a low doping concentration (19 cm-3 ). However, FLP with a Xenon (Xe) lamp (lamp duration: 3 ms; energy density: 56 J/cm2 ) raised the surface temperature to nearly 800 °C. Furthermore, high concentrations of both P and Sb (>1 × 1020 cm-3 ) were achieved at the surface. Our findings suggest that the FLP with high energy in a short amount of time (~3 ms) can create the peak power effect and the co-doping effect. The evidence shows that these effects contribute to enhancing n-type doping levels in the Ge structure