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52 protocols using h1299

1

Culturing Human Lung Cancer Cells

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Human normal bronchial epithelial cell line (BEAS-2B) and NSCLC cell lines (H1650, H1299,
A549, H1975, and HCC827) were obtained from the Shanghai Cell Bank of Chinese Academy of
Sciences (Shanghai, China). BEAS-2B cell line and NSCLC cells were maintained in RPMI1640
(Gibco, Grand Island, NY, USA) supplemented with 10% fetal bovine serum (FBS, Gibco, Grand
Island, NY, USA), 100 μg/ml streptomycin, and 100 U/ml penicillin (Invitrogen, Carlsbad,
CA, USA) at 37˚C with 5% CO2 .
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2

NSCLC Cell Line Cultivation Protocol

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The human NSCLC cell lines A549, H460, H292, H1299, Calu1, and SK-MES-1 were obtained from the Shanghai Cell Bank (Shanghai, China). The HBE cell line was purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). Cells were cultured in RPMI 1640 (Invitrogen, Carlsbad, CA, USA) containing 10% fetal bovine serum (FBS; Invitrogen, Carlsbad, CA, USA) at 37 °C in 5% CO2.
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3

Lung Cancer Cell Line Cultivation

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The human lung cancer cell lines, A549 and H1299, were obtained from the Shanghai Cell Bank (Shanghai, China) and authenticated by short tandem repeat DNA profiling. All cells were cultured in the Roswell Park Memorial Institute-1640 medium, 100 U/mL penicillin, and 100 μg/mL streptomycin (Sigma-Aldrich Co.) at 37°C and 5% CO2 in a high humidity. VP (S1786) was purchased from Selleckchem (Shanghai, China).
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4

Culturing NSCLC Cell Lines A549 and H1299

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We purchased NSCLC cell lines A549 and H1299 from the Shanghai Cell Bank of the Chinese Academy of Sciences (China). The two cell lines were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing 10% fetal bovine serum and placed in a constant temperature incubator at 37°C with 5% CO2 and humidity saturation. The experiment was performed on cells in the logarithmic growth stage.
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5

Culturing Human NSCLC and Lung Epithelial Cells

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Human NSCLC cell lines (A549, H1299, PC-9, HCC827, and H1975) and the normal human lung epithelial cell line BEAS-2B were purchased from the Shanghai Cell Bank of the Chinese Academy of Sciences. All NSCLC cell lines were seeded in culture flasks and cultured in RPMI 1640 medium (Gibco, Thermo Fisher Scientific, Inc.) supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Gibco) at 37 °C in the presence of 95% O2 and 5% CO2. BEAS-2B cells were cultured in Dulbecco's modified Eagle's minimal essential medium (DMEM, Gibco) under consistent culture conditions.
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Cell Culture Protocols for Lung Cancer Research

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The human bronchial epithelium (HBE) cell line was obtained from the American Type Culture Collection. The LK2 cell line was obtained from the Japanese Collection of Research Bioresources Cell Bank. The PG-LH7 (LH7) cell line was a gift from Dr Jie Zheng (Department of Pathology, Peking University). The A549, H1299, BE1, H292 and H460 cell lines were obtained from the Shanghai Cell Bank. All cells were cultured in RPMI-1640 (Invitrogen; Thermo Fisher Scientific, Inc.) supplemented with 10% fetal bovine serum (FBS; Invitrogen; Thermo Fisher Scientific, Inc.), 100 IU/ml penicillin (Sigma-Aldrich; Merck KGaA), and 100 µg/ml streptomycin (Sigma-Aldrich; Merck KGaA) at 37˚C in 5% CO2.
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Cell Culture Protocols for NSCLC Research

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The human bronchial epithelial (HBE) cell line was obtained from the American Type Culture Collection (ATCC) (Manassas, VA, USA) and cultured in DMEM supplemented with 10% fetal bovine serum (FBS). Human NSCLC cell lines (H1299, H460, H292 and A549) were obtained from the Shanghai Cell Bank (Shanghai, China) and cultured in RPMI1640 medium supplemented with 10% FBS (Gibco, NY, USA). All cell lines were cultured in 5% CO2 at 37°C in a humidified incubator.
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8

Culturing Lung Cancer Cell Lines

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The human lung cancer cell lines A549, H460, H1299 and normal human bronchial epithelial cell line (HBE) were purchased from the Shanghai Cell Bank of Chinese Academy of Sciences. All cells were cultured in RPMI1640 cell culture medium containing 100 ml/L fetal bovine serum, 100 U/ml penicillin, 100 g/ml streptomycin and 2 mmol/L glutamine at 37°C with 5% CO2 in full humidity.
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Culturing Diverse Lung Cancer Cell Lines

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The HBE cell line was obtained from the American Type Culture Collection (ATCC; Manassas, VA, USA). The H1299, H460, A549, H292, and SK-MES-1 cell lines were purchased from the Shanghai Cell Bank (Shanghai, China). All of these cells were cultured in RPMI 1640 (Invitrogen, Carlsbad, CA, USA) containing 10% fetal bovine serum (Invitrogen, Carlsbad, CA, USA), 100 μg/ml streptomycin (Sigma, St Louis, MO, USA), and 100 IU/ml penicillin (Sigma, St Louis, MO, USA). Cells were passaged every other day using 0.25% trypsin (Invitrogen, Carlsbad, CA, USA).
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10

Characterization of NSCLC Cell Lines

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The HBE(human bronchial epithelioid cells)cell line was obtained from the American Type Culture Collection (ATCC); (Manassas, VA, USA). The LK2 cell line was a gift from H. Kijima (Department of Pathology and Bioscience, Hirosaki University Graduate School of Medicine, Japan). Other NSCLC cell lines, including A549, SPC, H1299, H292, H460 and H661, were purchased from the Shanghai Cell Bank (Shanghai, China). Under conditions of high humidity (37℃ and 5% CO2), all cells were cultured in RPMI 1640 (Invitrogen, Carlsbad, CA) supplemented with 10% foetal bovine serum (Gibco), 100 U/ml penicillin and 100 μg/ml streptomycin (Sigma‐Aldrich). All cell lines were identified using short tandem repeat DNA analysis.
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