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1.
Tumour Biol ; 39(10): 1010428317720863, 2017 Oct.
Article in English | MEDLINE | ID: mdl-29034775

ABSTRACT

Early recurrence is common after curative hepatectomy for hepatocellular carcinoma and is associated with poor prognosis. This study aimed to identify risk factors of early recurrence after curative hepatectomy in hepatocellular carcinoma. Overall, 63 patients who underwent curative hepatectomy for hepatocellular carcinoma were enrolled. Patients were divided into the early recurrence group, who developed recurrence within 12 months after hepatectomy (n = 10), and the non-early recurrence group (n = 53). Clinicopathological factors of early recurrence were retrospectively analyzed. Among the 63 patients, 10 (15.9%) patients experienced early recurrence. Univariate analysis showed tumor necrosis (p = 0.012), level of PIVKA-II (prothrombin induced by vitamin K absence or antagonist-II; p = 0.002), and microvascular invasion (p = 0.029) to be associated with early recurrence. By multivariate analysis, there were significant differences in high PIVKA-II (p < 0.001) and tumor necrosis (p = 0.012) in patients with early recurrence. The optimal cutoff values of PIVKA-II and tumor necrosis were 46 mAU/mL and 3% of total tumor volume, respectively. Patients with a high preoperative PIVKA-II level and extent of tumor necrosis, which are independent risk factors for early recurrence, should be actively treated and monitored closely after hepatectomy.


Subject(s)
Carcinoma, Hepatocellular/pathology , Carcinoma, Hepatocellular/surgery , Liver Neoplasms/pathology , Liver Neoplasms/surgery , Neoplasm Recurrence, Local/etiology , Neoplasm Recurrence, Local/pathology , Biomarkers/metabolism , Carcinoma, Hepatocellular/metabolism , Female , Hepatectomy/methods , Humans , Liver Neoplasms/metabolism , Male , Microvessels/metabolism , Microvessels/pathology , Middle Aged , Multivariate Analysis , Necrosis/metabolism , Necrosis/pathology , Neoplasm Invasiveness/pathology , Neoplasm Recurrence, Local/metabolism , Protein Precursors/metabolism , Prothrombin/metabolism , Retrospective Studies , Risk Factors
2.
Transfus Apher Sci ; 56(3): 385-388, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28366590

ABSTRACT

INTRODUCTION: Therapeutic plasma exchange (TPE) is used for temporary support of liver function in patients presenting with early graft dysfunction after liver transplantation (LT) or liver surgery. We analyzed the effect of therapeutic apheresis on patients with liver disease. METHODS: Between January 2011 and August 2016, 93 apheresis procedures were performed for 26 patients at our institution. Anti-ABO isoagglutination immunoglobulin (Ig) M titer was checked using a type A and type B 3% red blood cell (RBC) suspension in saline with two-fold serial dilutions of patient serum. Anti-ABO isoagglutination IgG titer was checked by a type A and B 0.8% RBC suspension using a low-ionic strength/Coombs card. RESULTS: ABO-incompatible (ABOi) LT was the most common (n=10, 38.5%) indication for apheresis; early graft dysfunction after LT (n=8, 30.7%) was the second most common. Median initial IgM and IgG anti-ABO titers for ABOi LT recipients were 1:16 (range, 1:8-1:128) and 1:48 (range, 1:8-1:2048). We performed preoperative TPE in 10 recipients (median number of sessions, 1.5; range, 1-11). Among patients with early graft dysfunction, those who underwent living donor LT had better survival (4/4; 100%) than those who underwent nonliving donor LT (0/3; 0%). Patients who underwent living donor LT first and then additional LT also survived after three TPE sessions. CONCLUSION: Therapeutic apheresis is associated with a good survival rate and is essential for liver support in patients with early graft dysfunction after LT or posthepatectomy liver failure and during preparation for ABOi LT.


Subject(s)
Blood Component Removal/methods , Liver Transplantation/methods , Liver/pathology , Plasma Exchange/methods , Aged , Female , Humans , Male , Middle Aged
3.
Plant Mol Biol ; 65(1-2): 125-36, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17619151

ABSTRACT

Increasing its root to shoot ratio is a plant strategy for restoring water homeostasis in response to the long-term imposition of mild water stress. In addition to its important role in diverse fundamental processes, indole-3-acetic acid (IAA) is involved in root growth and development. Recent extensive characterizations of the YUCCA gene family in Arabidopsis and rice have elucidated that member's function in a tryptophan-dependent IAA biosynthetic pathway. Through forward- and reverse-genetics screening, we have isolated Tos17 and T-DNA insertional rice mutants in a CONSTITUTIVELY WILTED1 (COW1) gene, which encodes a new member of the YUCCA protein family. Homozygous plants with either a Tos17 or T-DNA-inserted allele of OsCOW1 exhibit phenotypes of rolled leaves, reduced leaf widths, and lower root to shoot ratios. These phenotypes are evident in seedlings as early as 7-10 d after germination, and remain until maturity. When oscow1 seedlings are grown under low-intensity light and high relative humidity, the rolled-leaf phenotype is greatly alleviated. For comparison, in such conditions, the transpiration rate for WT leaves decreases approx. 5- to 10-fold, implying that this mutant trait results from wilting rather than being a morphogenic defect. Furthermore, a lower turgor potential and transpiration rate in their mature leaves indicates that oscow1 plants are water-deficient, due to insufficient water uptake that possibly stems from that diminished root to shoot ratio. Thus, our observations suggest that OsCOW1-mediated IAA biosynthesis plays an important role in maintaining root to shoot ratios and, in turn, affects water homeostasis in rice.


Subject(s)
Homeostasis , Multigene Family/genetics , Oryza/enzymology , Oxygenases/metabolism , Plant Roots/enzymology , Plant Shoots/enzymology , Water/metabolism , Amino Acid Sequence , DNA, Bacterial/genetics , Gene Expression Regulation, Enzymologic , Gene Expression Regulation, Plant , Genes, Plant/genetics , Indoleacetic Acids/metabolism , Molecular Sequence Data , Mutation/genetics , Oryza/genetics , Oryza/growth & development , Oxygenases/chemistry , Oxygenases/classification , Oxygenases/genetics , Phenotype , Phylogeny , Plant Roots/genetics , Plant Roots/growth & development , Plant Shoots/genetics , Plant Shoots/growth & development , Sequence Alignment , Sequence Homology, Amino Acid , Tryptamines/biosynthesis
4.
J Plant Physiol ; 160(4): 347-53, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12756914

ABSTRACT

To analyze the physiological role of dehydroascorbate reductase (DHAR, EC 1.8.5.1) catalyzing the reduction of DHA to ascorbate in environmental stress adaptation, T1 transgenic tobacco (Nicotiana tabacum cv. Xanthi) plants expressing a human DHAR gene in chloroplasts were biochemically characterized and tested for responses to various stresses. Fully expanded leaves of transgenic plants had about 2.29 times higher DHAR activity (units/g fresh wt) than non-transgenic (NT) plants. Interestingly, transgenic plants also showed a 1.43 times higher glutathione reductase activity than NT plants. As a result, the ratio of AsA/DHA was changed from 0.21 to 0.48, even though total ascorbate content was not significantly changed. When tobacco leaf discs were subjected to methyl viologen (MV) at 5 mumol/L and hydrogen peroxide (H2O2) at 200 mmol/L, transgenic plants showed about a 40% and 25% reduction in membrane damage relative to NT plants, respectively. Furthermore, transgenic seedlings showed enhanced tolerance to low temperature (15 degrees C) and NaCl (100 mmol/L) compared to NT plants. These results suggest that a human derived DHAR properly works for the protection against oxidative stress in plants.


Subject(s)
Adaptation, Physiological , Nicotiana/genetics , Oxidoreductases/genetics , Plants, Genetically Modified/genetics , Cold Temperature , Humans , Hydrogen Peroxide/pharmacology , Paraquat/pharmacology , Plant Leaves/drug effects , Plants, Genetically Modified/metabolism , Plants, Genetically Modified/physiology , Sodium Chloride/administration & dosage , Nicotiana/metabolism , Nicotiana/physiology
5.
Philos Trans R Soc Lond B Biol Sci ; 357(1426): 1441-49; discussion 1449-50, 1469-70, 2002 Oct 29.
Article in English | MEDLINE | ID: mdl-12437883

ABSTRACT

Photoinactivation of photosystem II (PSII), the light-induced loss of ability to evolve oxygen, is an inevitable event during normal photosynthesis, exacerbated by saturating light but counteracted by repair via new protein synthesis. The photoinactivation of PSII is dependent on the dosage of light: in the absence of repair, typically one PSII is photoinactivated per 10(7) photons, although the exact quantum yield of photoinactivation is modulated by a number of factors, and decreases as fewer active PSII targets are available. PSII complexes initially appear to be photoinactivated independently; however, when less than 30% functional PSII complexes remain, they seem to be protected by strongly dissipative PSII reaction centres in several plant species examined so far, a mechanism which we term 'inactive PSII-mediated quenching'. This mechanism appears to require a pH gradient across the photosynthetic membrane for its optimal operation. The residual fraction of functional PSII complexes may, in turn, aid in the recovery of photoinactivated PSII complexes when conditions become less severe. This mechanism may be important for the photosynthetic apparatus in extreme environments such as those experienced by over-wintering evergreen plants, desert plants exposed to drought and full sunlight and shade plants in sustained sunlight.


Subject(s)
Light , Photosynthetic Reaction Center Complex Proteins/metabolism , Photosynthetic Reaction Center Complex Proteins/radiation effects , Energy Transfer , Hydrogen-Ion Concentration , Kinetics , Photosystem II Protein Complex , Plant Diseases , Plant Physiological Phenomena
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