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Liquid biopsy, particularly circulating tumor DNA (ctDNA), has drawn a lot of attention as a non- or minimal-invasive detection approach for clinical applications in patients with cancer. Many hematological malignancies are well suited for serial and repeated ctDNA surveillance due to relatively high ctDNA concentrations and high loads of tumor-specific genetic and epigenetic abnormalities. Progress of detecting technology in recent years has improved sensitivity and specificity significantly, thus broadening and strengthening the potential utilities of ctDNA including early diagnosis, prognosis estimation, treatment response evaluation, minimal residual disease monitoring, targeted therapy selection, and immunotherapy surveillance. This manuscript reviews the detection methodologies, clinical application and future challenges of ctDNA in hematological malignancies, especially for lymphomas, myeloma and leukemias.
RESUMO
Rhubarb plants (Rheum officinale and R. tanguticum) have edible stalks. In this work, we aimed to compare the nutritional properties, chemical compositions, and bioactivities of R. officinale (SRO) and R. tanguticum (SRT) stalks and to analyze the composition-function relationship. Results showed that the two stalks were good sources of fiber, as well as minerals. They contained abundant essential amino acids and essential fatty acids to regulate the immunity and prevent some chronic diseases; the contents of polyunsaturated fatty acids were 2,244.32 mg/100 g and 2,844.69 mg/100 g, respectively. The antioxidant activity were also proved. Metabolomics showed that SRO and SRT contained abundant phenolic acids. Due to the higher concentrations of flavones, SRT has better antiinflammatory activities than SRO by inhibiting NF-κB signaling pathway. Rhubarb stalks exhibited good safety in acute toxicity and cytotoxicity tests. This work indicated that the two stalks have nutritional value, safety, and bioactivities, and could be used as sources of nutritional ingredients for regulating the immunity of body in food industry.
RESUMO
OBJECTIVE: To investigate the changes and its clinical significance of the expressions of the mRNA and protein of heat shock protein 70 (HSP70) and heme oxygenase-1 (HO-1) genes in the myocardium of acute myocardial infarction (AMI) areas in patients who died suddenly due to AMI. METHODS: Specimens of myocardial tissue at infarct site was obtained during autopsy from 18 patients who died suddenly due to AMI, and they were enlisted as study group, and that of myocardial tissue from 17 normal hearts of patients died rapidly after accidents were as control group. The levels of mRNA expression of HSP70 and HO-1 genes were measured in all the specimens by reverse transcription-polymerase chain reaction (RT-PCR) using cDNA samples, and the levels and locations of HSP70 and HO-1 protein expressions in myocardial cells of all specimens were examined by immunohistochemistry (IHC), and the pathological changes in the myocardial tissue were observed. RESULTS: The expressions of HSP70 mRNA (0.841+/-0.058), HO-1 mRNA (0.918+/-0.161) and HSP70 protein (3 556.68+/-574.19), HO-1 protein (4 336.68+/-865.30) in the myocardium of the AMI areas in the study group were significantly higher than those in control group (the expressions of HSP70 mRNA: 0.105+/-0.034, HO-1 mRNA: 0.086+/-0.053, HSP70 protein: 289.21+/-68.51, HO-1 protein: 1 556.78+/-506.26, all P<0.01), and a weak expression of HSP70 and HO-1 protein was found in the cardiocytes of the AMI area in study group. In the control group, HSP70 protein expression was negative in the cardiocytes, and there was a weak expression of HO-1 protein in the cardiocytes. There was a significant positive correlation between the expressions of mRNA and protein of HSP70 and HO-1 genes at the cardiocytes of patients died suddenly of AMI in study group (r(1)=0.865, r(2)=0.816, both P<0.01). CONCLUSION: HSP70 and HO-1 probably were both involved in the pathological and physiological processes of AMI, while HO-1 may express in cardiocytes, but it is more abundant in the cardiocytes in the AMI area.