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3 protocols using tu212

1

Cell Culture Protocols for Respiratory and Cancer Cell Lines

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Human bronchial epithelioid cells (16‐HBE) and human laryngeal cancer cells (TU212 and AMC‐HN‐8) were obtained from the BeNa Culture Collection (BNCC), all of which were cultured routinely in high glucose Dulbecco's modified Eagle's medium (H‐DMEM, HyClone) containing 10% fetal bovine serum (Biological Industries). Human umbilical vein endothelial cells (HUVECs) were purchased from the American Type Culture Collection (ATCC) and were cultured in endothelial cell medium (ECM; ScienCell). When the cells reached 90% confluency, they were passaged with a 0.25% trypsin‐EDTA solution (Beyotime Biotechnology). The cells were cultured in a humidified incubator at 37°C under an atmosphere with 5% CO2 in air (Thermo Fisher).
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Laryngeal Squamous Cell Carcinoma Specimens

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The paraffin-embedded specimens of 110 LSCC, 30 noncancerous tissues and 30 tissues of laryngeal severe dysplasia were kindly acquired from the Pathology Department in the Second Affiliated Hospital of Harbin Medical University. All 110 LSCC patients were diagnosed by professional pathologist, and were all initially treated by partial or total laryngectomy at the Otorhinolaryngology Department, the Second Affiliated Hospital of Harbin Medical University from February 2008 to October 2012. 74 LSCC patients among them, who underwent tumor recurrence after surgery, had received chemotherapy for further treatment. All 110 patients were followed up for at least 5 years. In addition, 30 paired LSCC and adjacent noncancerous tissues were kindly obtained from patients and were snap frozen in liquid nitrogen within 15 min after excision. All patients provided written informed consent in accordance with the Declaration of Helsinki. The study was approved by the Ethics Committee of The Second Affiliated Hospital of Harbin Medical University. The laryngeal carcinomas cell lines (AMC-HN8, TU212, TU686)32 (link) were provided by BeNa Culture Collection (Jiangsu, China). Cells were cultured in DMEM medium (Invitrogen, Carlsbad, CA) containing 10% fetal bovine serum (PAN-Biotech, Adenbach, Germany) and incubated in a humidified 37 °C incubator with 5% CO2.
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LSCC Cell Lines and Tissue Samples

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Four LSCC cell lines (AMC-HN-8, HEP-2, TU-212 and TU-686) and the normal bronchial epithelial cell line NHBEC were purchased from Bena Culture Collection (Beijing, China). HEK293T cell line was purchased from American Type Culture Collection (ATCC) (Gaithersburg, MD, USA). All cell lines were cultured in DMEM medium (HyClone, Logan, Utah, USA) containing 10% fetal bovine serum (Biological Industries, Beit HaEmek, Israel) . Thirty pairs of primary LSCC paracancerous and cancerous tissues were collected from Chengde Central Hospital (Chengde, Hebei, China). All patients were pathologically confirmed, and the fresh tissues were immediately collected and frozen in liquid nitrogen after surgery. The collection of tissues was approved by the Review and Ethics committee of Chengde Central Hospital. Nuciferine (Purity, 99.49%) and other 49 natural products used in this study were all obtained from Selleck Chemicals (Houston, Texas, USA).
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