The absorbance of the solution was read at a wavelength of 540 nm using a microplate reader (BIO-RAD550; BIO-RAD, Tokyo, Japan). The percentage inhibition was determined by comparing the cell density of the see more drug-treated cells with that of untreated controls. All experiments were repeated at least 3 times. Specimens and blood samples We evaluated 100 patients with gastric cancer (cases) who were treated with curative gastrectomy and standard lymph node dissection at the Gastroenterological Surgery Department, Kanazawa University Hospital,
Ishikawa, from 2002 to 2009. The study was approved by the ethics committee of Kanazawa University, and informed consent was obtained from each patient before enrollment in this study. All resected primary tumors and regional lymph nodes were histologically evaluated by H&E staining according Erismodegib mw to the Japanese Classification of Gastric Carcinoma [30]. A fasting morning blood sample was obtained for the adiponectin assay from each patient after admission into the study. Samples were also obtained from 10 healthy volunteer controls. Weight and height of each patient was recorded by medical staff. BMI was calculated as weight in kilograms divided by height in square
meters. Medical staff measured all data. Serum adiponectin measurement All blood samples were immediately separated by centrifugation and stored at -80°C until use. A quantitative JAK inhibitor sandwich enzyme-linked immunosorbent assay technique with a Quantikine human adiponectin immunoassay kit (R&D Systems, Inc., Minneapolis, NM, USA) was used in accordance with the manufacturer’s instructions. All experiments were performed in triplicate. Immunohistochemical staining All surgically obtained specimens were fixed in 10% neutral buffered formalin, embedded in paraffin, and cut into 4-μm-thick serial sections. In brief, the slides were immersed in methanol containing 0.3% H2O2 for 30 min, blocked with 3.3% normal Reverse transcriptase goat serum in PBS, and incubated with the anti-AdipoR1 antibody (C-14, goat polyclonal IgG, diluted 1:100; Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA) and anti-AdipoR2 (C-12, goat polyclonal
IgG, diluted 1:100; Santa Cruz) at 4°C overnight. After the sections were washed in PBS, immunoreactivity was visualized by EnVision reagent (Dako Co., Kyoto, Japan). Slides were examined under low power (×40) to identify the brown staining precipitates within the cytoplasm of cancer cells. Sections that showed same or higher staining than that of the normal gastric mucosa and more than 10% of cancerous tissue stained under a ×100 field were considered positive samples. Statistical analysis Values are expressed as means ± standard error (SE). Differences in the cell growth assay were determined by one-way analysis of variance (ANOVA). The relationship between serum adiponectin level and BMI or clinical stage of gastric cancer was evaluated using the Mann-Whitney U test.