8 research outputs found
Effects of climate change and human activities on runoff and sediment inputs of the largest freshwater lake in China, Poyang Lake
<p>The nonparametric Mann-Kendall test and the Pettitt test were employed to examine the change trends and shifts of runoff and sediment input to Poyang Lake between 1961 and 2013. Water balance and linear regression models were used to evaluate the impacts of climate variability and human activities on the runoff and sediment discharge changes. The results showed that runoff inputs to the lake had insignificant temporal trends and change points, while sediment inputs had significant decreasing trends, with an abrupt change in 1989. Quantitative assessment demonstrated that human activities led to a small decrease (5.5%) in runoff inputs to the lake, and a dramatic (121.4%) decrease in sediment inputs to the lake between the reference period (before the change point) and the human-influenced period (after the change point). This work provides a useful reference for future policy makers in water resource utilization and environmental safety of the Poyang Lake basin.</p
Lactate Dehydrogenase B Is Associated with the Response to Neoadjuvant Chemotherapy in Oral Squamous Cell Carcinoma
<div><p>Oral squamous cell carcinoma (OSCC) comprises a subset of head and neck squamous cell carcinoma (HNSCC) with poor therapeutic outcomes and high glycolytic dependency. Neoadjuvant chemotherapy regimens of docetaxel, cisplatin and 5-fluorouracil (TPF) are currently accepted as standard regimens for HNSCC patients with a high risk of distant metastatic spread. However, the antitumor outcomes of TPF neoadjuvant chemotherapy in HNSCC remain controversial. This study investigated the role of lactate dehydrogenase B (LDHB), a key glycolytic enzyme catalyzing the inter-conversion between pyruvate and lactate, in determining chemotherapy response and prognosis in OSCC patients. We discovered that a high protein level of LDHB in OSCC patients was associated with a poor response to TPF regimen chemotherapy as well as poor overall survival and disease-free survival. Our in-depth study revealed that high LDHB expression conferred resistance to taxol but not 5-fluorouracil or cisplatin. LDHB deletion sensitized OSCC cell lines to taxol, whereas the introduction of LDHB decreased sensitivity to taxol treatment. Taxol induced a pronounced impact on LDHB-down-regulated OSCC cells in terms of apoptosis, G2/M phase cell cycle arrest and energy metabolism. In conclusion, our study highlighted the critical role of LDHB in OSCC and proposed that LDHB could be used as a biomarker for the stratification of patients for TPF neoadjuvant chemotherapy and the determination of prognosis in OSCC patients.</p></div
Knockdown of LDHB enhances taxol-induced apoptosis.
<p>(<b>A, B</b>) KB cells and HN12 cells were transfected with scrambled or LDHB siRNA and treated with DMSO or 10 nM taxol for 48 h. <b>(C)</b> HN30 cells were transfected with empty vector or LDHB and treated with DMSO or taxol for 48 h at the indicated concentrations. Quantification results of three independent experiments are shown on the right side.</p
Combination of taxol and LDHB down-regulation exhibits a synergistic effect on cell metabolism.
<p>KB and HN12 cells were transfected with scramble or LDHB siRNA and then treated with DMSO or taxol of 10 nM for 24 h. (<b>A, B</b>) ECAR was measured by an XF96 analyzer. (<b>C, D</b>) OCR was measured by an XF96 analyzer. (<b>E, F</b>) Cell lysates were prepared, and the intracellular ATP level was determined. *<i>P</i> < 0.05, compared to the control group; <sup>#</sup><i>P</i> < 0.05, compared to the taxol group. Mean ± SE (n = 3).</p
LDHB impacts the efficacy of taxol.
<p>(A, B) KB and HN12 cells were transfected with scrambled or LDHB siRNA. (A) After 72 h, LDHB expression was examined, and LDH activity was measured. (B) After 48 h, cells were washed with PBS twice followed by the addition of fresh serum-free media and extracellular lactate amount was measured at 12 h post-incubation. (C, D) KB and HN12 cells were transfected with scrambled or LDHB siRNA and then treated with DMSO or taxol for 72 h at the indicated concentrations, and cell viability was measured. (E) The LDHB stable-interference strains of KB cells were established and verified by western blotting; the clonogenic assay was conducted in shCON and shLDHB KB cells exposed to 0.5 nM taxol. (F) HN30 cells were transfected with empty vector or LDHB and treated with DMSO or taxol for 72 h at the indicated concentrations. *<i>P</i> < 0.05, compared to the control group. Mean ± SE (n = 3).</p
Knockdown of LDHB induces the mitochondrion-dependent apoptosis pathway.
<p>KB cells were transfected with scrambled or LDHB siRNA and then treated with DMSO or 10 nM taxol for 24 h. (<b>A</b>) The mitochondria and the cytoplasm were separated and measured for cytochrome C by western blotting. COX IV was used as a marker for mitochondria. (<b>B</b>) Mitochondrial cytochrome C was measured by FACS analysis. (<b>C</b>) Cell lysates were prepared for western blotting. GAPDH was used as a loading control.</p
Correlations between LDHB and pathological parameters.
<p>*Statistically significant difference.</p><p>Correlations between LDHB and pathological parameters.</p
LDHB is associated with prognosis and TPF induction chemotherapy in OSCC patients.
<p>(A) Representative images of immunohistochemical staining for LDHB expression in OSCC patients. (B, C) The correlation of LDHB expression with overall survival and disease-free survival in OSCC patients (n = 107), as determined by Kaplan-Meier survival analysis. The <i>P</i> value was calculated using the log-rank test. (D) The correlation between LDHB expression and TPF induction chemotherapy efficacy in OSCC patients, as determined by cross-table analysis (n = 50).</p