The cornerstone of integrating circulating tumor DNA into cancer management

Recent circulating tumor DNA (ctDNA) research has demonstrated its potential as a non-invasive biomarker for cancer. However, the deployment of ctDNA assays in routine clinical practice remains challenging owing to variability in analytical approaches and the assessment of clinical significance. A well-developed, analytically valid ctDNA assay is a prerequisite for integrating ctDNA into cancer management, and an appropriate analytical technology is crucial for the development of a ctDNA assay. Other determinants including pre-analytical procedures, test validation, internal quality control (IQC), and continual proficiency testing (PT) are also important for the accuracy of ctDNA assays. In the present review, we will focus on the most widely used ctDNA detection technologies and the key quality management measures used to assure the accuracy of ctDNA assays. The aim of this review is to provide useful information for technology selection during ctDNA assay development and assure a reliable test result in clinical practice.     

Analysis of Plankton Dynamics in a Southwestern U.S.A. Reservoir Using ATP Assays

Plankton biomass in size segregated (i.e. 0.45–10 μm, 10–64 μm, 64–165 μm, and > 165 μm) samples was measured using ATP assays for two years in H. H. Moss Reservoir. The presence of variable numbers of microcrustacean zooplankton in the > 165 μ size class introduced significant, and perhaps inaccurate, variance into temporal dynamics of total ATP concentrations. As many as six physiochemical parameters, measured during 1975–76, were required to produce a significant multiple regression against ATP concentrations; a significant correlation between total ATP measured in the photic zone and surface temperature was observed. A large standing crop of nannoplankton (i.e. 0.45–10 μm) existed in the anaerobic and aphotic hypolimnion during summer stratification both years. This suggested that microbial heterotrophy was an especially important primary trophic event in the reservoir. Particulate (POC) and dissolved (DOC) organic carbon were measured in 1976–77. Organic carbon (POC + DOC) regressed significantly against ATP concentration in the 0.45–10 μm size class and microbial biomass (i.e. 0.45–165 μm) averaged 32 per cent of POC. When biomass was monitored over 24-hour periods in the photic zone, significant changes were documented in various size classes, especially nannoplankton; but total microbial biomass remained relatively constant.     

Influence of the growth conditions on the hydrophobicity of Renibacterium salmoninarum evaluated by different methods

The influence of medium and salinity on the cell surface hydrophobicity of Renibacterium salmoninarum was investigated using three different methods: bacterial adherence to hydrocarbons (BATH), salt agglutination test (SAT), and binding to nitrocellulose filters (NCF). The possible relationship among hydrophobicity, haemagglutination and adherence to cell lines was also evaluated. R. salmoninarum showed to be highly hydrophobic regardless of the growth conditions or technique employed. Nevertheless, slight differences can be detected depending on the method used. In the SAT and NCF assays very uniform values were obtained within the strains. All the R. salmoninarum isolates agglutinated in (NH4)2SO4 in a range of 0.05-0.2 M and displayed a 77-100% of adherence to nitrocellulose filters. However, more variable results were observed in the BATH method depending on the hydrocarbon, buffer and strain employed. Although all of the isolates produced haemagglutinins for homeotherm erythrocytes, the majority of them failed to agglutinate poikilothermic red blood cells and were unable to adhere to fish cell lines. Therefore, a general correlation among hydrophobicity, agglutinating capacity for fish erythrocytes and adherence to fish cells can not be established for R. salmoninarum.     

Autocrine growth factor and spontaneous transformation of rat liver epithelial cells

Summary Liver epithelial cells from a young rat were cultured and passaged for a long period until they showed a malignant transformation (tumorigenicity in athymic mice), to know when an autocrine growth factor is produced in the course of a spontaneous malignant transformation of normal cells in vitro. The cells initially showed a cellular transformation and an increased growth rate, then produced an autocrine growth factor after Passage 55, and finally the cells after Passage 105 showed a malignant transformation (tumorigenicity in vivo). It is suggested that in addition to an autocrine growth factor, some other factors might be related to a malignant transformation (tumorigenicity in vivo).