ABSTRACT
Purpose: The spatial heterogeneity of phenotypic and molecular characteristics of CTCs within the circulatory system remains unclear. Herein, we mapped the distribution and characterized biological features of CTCs along the transportation route in hepatocellular carcinoma (HCC).Experimental Design: In 73 localized HCC patients, blood was drawn from peripheral vein (PV), peripheral artery (PA), hepatic veins (HV), infrahepatic inferior vena cava (IHIVC), and portal vein (PoV) before tumor resection. Epithelial and mesenchymal transition (EMT) phenotype in CTCs were analyzed by a 4-channel immunofluorescence CellSearch assay and microfluidic quantitative RT-PCR. The clinical significance of CTCs from different vascular sites was evaluated.Results: The CTC number and size gradient between tumor efferent vessels and postpulmonary peripheral vessels was marked. Tracking the fate of CTC clusters revealed that CTCs displayed an aggregated-singular-aggregated manner of spreading. Single-cell characterization demonstrated that EMT status of CTCs was heterogeneous across different vascular compartments. CTCs were predominantly epithelial at release, but switched to EMT-activated phenotype during hematogeneous transit via Smad2 and ß-catenin related signaling pathways. EMT activation in primary tumor correlated with total CTC number at HV, rather than epithelial or EMT-activated subsets of CTCs. Follow-up analysis suggested that CTC and circulating tumor microemboli burden in hepatic veins and peripheral circulation prognosticated postoperative lung metastasis and intrahepatic recurrence, respectively.Conclusions: The current data suggested that a profound spatial heterogeneity in cellular distribution and biological features existed among CTCs during circulation. Multivascular measurement of CTCs could help to reveal novel mechanisms of metastasis and facilitate prediction of postoperative relapse or metastasis pattern in HCC. Clin Cancer Res; 24(3); 547-59. ©2017 AACR.
Subject(s)
Carcinoma, Hepatocellular/diagnosis , Epithelial-Mesenchymal Transition , Liver Neoplasms/diagnosis , Neoplastic Cells, Circulating/metabolism , Neoplastic Cells, Circulating/pathology , Biomarkers, Tumor , Carcinoma, Hepatocellular/etiology , Carcinoma, Hepatocellular/mortality , Cell Count , Epithelial-Mesenchymal Transition/genetics , Flow Cytometry , Gene Expression Profiling , Hemodynamics , Humans , Immunohistochemistry , Liver Neoplasms/etiology , Liver Neoplasms/mortality , Neovascularization, Pathologic/genetics , Neovascularization, Pathologic/metabolism , Phenotype , Prognosis , Shear StrengthABSTRACT
Wheat hybrid necrosis is caused by the interaction of two dominant complementary genes, Ne1 and Ne2, located on chromosome arms 5BL and 2BS, respectively. The sequences of Ne1 or Ne2 have not yet been identified. It is also not known whether Ne1 and Ne2 are structural or regulatory genes. Understanding the proteomic pathways may provide a knowledge base for protecting or maximizing the photosynthesis capacity of wheat. Using DIGE and MALDITOF- TOF MS, the flag leaf protein patterns of the two unique F14 near-isogenic line siblings (NILs), the necrotic ShunMai 12Ah (Ne1Ne1Ne2Ne2) and the normal ShunMai 12Af (Ne1Ne1ne2ne2) were compared. Due to the presence or absence of Ne2, (i) three protein spots were expressed or disappeared, (ii) seven RuBisCO-related proteins were altered significantly, and (iii) 21 photosynthesis/glucose related proteins were changed significantly. Three hypotheses were deduced, (i) Ne1 may also encode protein(s), (ii) genetic maladjustment of RuBisCO could lead to early leaf death, and (iii) interactions between nuclear genes and chloroplast genes could determine photosynthetic traits. Our hypothetical model presents the RuBisCO pathway of hybrid necrosis in wheat and explains how Ne1 and Ne2 interact at molecular level.
Subject(s)
Plant Diseases/genetics , Proteomics , Ribulose-Bisphosphate Carboxylase/genetics , Triticum/genetics , Genotype , Phenotype , Photosynthesis/genetics , Plant Leaves/genetics , Plant Leaves/metabolism , Triticum/growth & developmentABSTRACT
OBJECTIVE: To evaluate the molluscicidal effect of Rongbao in schistosomiasis endemic areas in Mianyang City. METHODS: Three Oncomelania hupensis snail habitats with the similar snail status were selected and sprayed with Rongbao, niclosamide, and fresh water, respectively. Then the snail status in the three fields was surveyed before the spraying and 7, 15, 30 and 60 days after the spraying, and the molluscicidal effects of different molluscicides were compared. RESULTS: The reducing rates of densities of living snails in the field sprayed with Rongbao were 94.4%, 95.9%, 98.2% and 98.8%, 7, 15, 30 and 60 days after the spraying, respectively. The reducing rates of the densities of living snails in the other field sprayed with niclosamide were 94.0%, 94.0%, 89.9% and 92.2% in above-mentioned days, respectively. In the 30 days and 60 days after the spraying, the reducing rates of densities of living snails in the field sprayed with Rongbao were significantly higher than those sprayed with niclosamide (chi2(30d) 8.18, chi2(60d) = 3.97, Both P < 0.05). CONCLUSION: The short-term molluscicidal effect of Rongbao is similar to that of niclosamide, but the long-term effect of Rongbao is better than that of niclosamide.
Subject(s)
Cities , Molluscacides , Snails , Animals , Chemistry, Pharmaceutical , China , Molluscacides/chemistryABSTRACT
Wheat hybrid necrosis has been genetically characterised for many years, but the specific gene(s) and the protein products involved in the processes remains unknown. In this study, protein expression in the base (B), mid (M) and tip (T) segments of the FL-2 leaves of a necrotic hybrid, PZF1 and its parents, Pan555 and Zheng891, was analysed and compared using a high throughput proteomic approach. Twenty-three protein spots, with significant variations in intensity across the necrotic leaf segments, were analysed by MALDI-TOF-MS, of which, 18 were matched to protein accessions in the NCBI database. Several of these proteins are enzymes involved in the methylation cycle, including AdoHcy hydrolase, AdoMet synthase 3 and methionine synthase 1; AdoHcy hydrolase was downregulated sharply in M and T, and AdoMet synthase 3 and methionine synthase 1 were upregulated gradually from M to T. This result suggests that methylation-associated processes, including epigenetic mechanisms, may play a role in the initiation and development of hybrid necrosis. Several energy cycle-associated proteins and cytoprotective proteins were also differentially expressed across the leaf segments, suggesting their direct association with or possible involvement in the necrotic processes. The significant imbalance of a heat-shock protein, a transposon protein and a RNA- and ssDNA-binding protein also makes these proteins potential molecular components in the necrotic processes.