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Parthenolide

Manufactured by Santa Cruz Biotechnology
Sourced in United States

Parthenolide is a bioactive compound extracted from the feverfew plant (Tanacetum parthenium). It is a natural product with potential therapeutic applications. Parthenolide exhibits anti-inflammatory and anti-cancer properties, and is commonly used in scientific research for its specific biological activities. This compound is available as a laboratory reagent for use in various experimental settings.

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9 protocols using parthenolide

1

Parthenolide Suppresses TWEAK-Induced RANTES

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PAM212 cells (5×104) were washed with PBS and pre-treated for two hours with 10 μM parthenolide (Santa Cruz), wortmannin (Tocris Biosciences, Minneapolis, MN), or PD98059 (Cell Signaling, Beverly, MA), followed by Fc-TWEAK or control Ig for 48 hours. Supernatants were analyzed by RANTES ELISA.
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2

Cytotoxicity of Parthenolide and Cisplatin

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Parthenolide and cisplatin (Figure 1) were obtained from Santa Cruz Biotechnology (Dallas, USA). A549, PC9, H1299, and BEAS-2B cell lines were generously provided by the State Key Laboratory of Oncology in South China. They were cultivated in RPMI 1640 medium supplemented with 10% fetal bovine serum, L-glutamine, gentamycin, and penicillin/streptomycin, and cultured at 37°C in a humidified atmosphere containing 5% CO2.
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3

Investigating Inflammatory Responses in P. aeruginosa

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We obtained LPS derived from P. aeruginosa, dexamethasone (Dex), U 0126, phorbol 12-myristate 13-acetate (PMA), Adenosine triphosphate (ATP), and BITC from Sigma-Aldrich (St. Louis, MO, USA). SP 600126 was obtained from Enzo Life Sciences, Inc. (Farmingdale, NY, USA). BAY 11-7082 and parthenolide were obtained from Santa Cruz Biotechnology Inc. Cell Counting Kit-8 (CCK-8) was obtained from Dojindo Laboratories (Kumamoto, Japan). Antibodies against caspase-1 and pro-IL-1β were obtained from Abcam Inc. (Cambridge, MA, USA). Anti-NF-κB p65 antibodies were purchased from eBioscience (San Diego, CA, USA). Anti-NLRP-3 antibodies were obtained from AdipoGen (San Diego, CA, USA). Antibodies against extracellular signal-related kinase (ERK), phospho (p)-ERK, c-Jun N-terminal kinase (JNK), p-JNK, and p-IκB-α were obtained from Cell Signaling Technology, Inc. (Danvers, MA, USA). Anti-Lamin B antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Goat anti-rabbit IgG-horseradish peroxidase was obtained from A-Frontier (Seoul, Korea). The CellTiter-Glo® Luminescent assay was obtained from Promega (Madison, WI, USA).
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4

Signaling Pathway Inhibitors in LPS Activation

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We purchased LPS (Escherichia coli O111:B4) and U0126 (cat. number U120) from Sigma Chemical Co. (St. Louis, MO, USA). SP600125 (cat. number BML-EI305) and SB203580 (cat. number BML-EI286) were purchased from Enzo Life Sciences, Inc. (Farmingdale, NY, USA). LY294002 (cat. number 440202) was purchased from Calbiochem (La Jolla, CA, USA). SR11302 (cat. number SR-11032) was purchased from R&D Systems (Minneapolis, MN, USA). BAY 11-7082 and parthenolide were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Antibodies against c-Jun N-terminal kinase (JNK) (cat. number 9252), phospho- (p-) JNK (cat. number 9251), p-extracellular signal-related kinase (ERK) (cat. number 9106), Akt (cat. number 9272), p-Akt (cat. number 4058), and p-p38 mitogen-activated protein kinase (MAPK) (cat. number 9211) were purchased from Cell Signaling Technology, Inc. (Danvers, MA, USA). Antibodies against p38 MAPK (cat. number sc-535), ERK (cat. number sc-94), iNOS (cat. number sc-651), and COX-2 (cat. number sc-1745) were purchased from Santa Cruz Biotechnology.
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5

Isolation and Crystallization of Goyazensolide Compounds

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(–)-Goyazensolide (1), (–)-15-deoxygoyazensolide (2), (–)-ereglomerulide (3), and (+)-rufesolide A (4) were isolated from the leaves of Piptocoma rufescens in a previous study,5 (link) with their single crystals grown in a mixture of n-hexane and acetone by slow crystallization in each case. Parthenolide was purchased from Santa Cruz Biotechnology (Dallas, TX, USA). Paclitaxel, PKC412, and other reagents were purchased from Sigma-Aldrich (St. Louis, MO, USA). All procedures were carried out using solvents obtained from commercial sources and employed without further purification.
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6

Osteogenic Gene Expression Regulation

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Bsp and osteocalcin luciferase constructs with mouse-specific Bsp- and OC-promoter regions were kindly provided by Dr Renny Franceschi (University of Michigan, School of Dentistry) and Dr Chawnshang Chang (University of Rochester Medical Center).(37 (link),38 (link)) pGL3 empty vector and pcDNA-IKK (wild-type) plasmid were obtained from Addgene (Cambridge, MA, USA). Small molecule inhibitors BAY-117082 (10 μM) and parthenolide (10 μM) and siRNA against p65, p50, IKK-beta and HDAC1 were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Cells seeded in αMEM media containing 0.3% FBS were transfected with corresponding constructs using Lipofectamine 2000 (Invitrogen), followed by incubation with TNFα (10 ng/mL) and Bmp2 (100 ng/mL) for 48 hours. Luciferase reporter activity was measured using dual-luciferase reporter assay system (Promega, Madison, WI, USA) as described.(39 (link)) For mRNA assays, cells were lysed and mRNA was isolated using the RNeasy Mini kit (Qiagen, Valencia, CA, USA) and RTPCR was performed using SYBR Green (Applied Biosystems, Carlsbad, CA, USA) as described.(39 (link))
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7

Parthenolide Suppresses TWEAK-Induced RANTES

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PAM212 cells (5×104) were washed with PBS and pre-treated for two hours with 10 μM parthenolide (Santa Cruz), wortmannin (Tocris Biosciences, Minneapolis, MN), or PD98059 (Cell Signaling, Beverly, MA), followed by Fc-TWEAK or control Ig for 48 hours. Supernatants were analyzed by RANTES ELISA.
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8

Parthenolide Cytotoxicity in Gallbladder Cancer

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Parthenolide was purchased from Santa Cruz Biotechnology. The molecular structure of PTL is shown in Fig. 1. The GBD-SD and NOZ gallbladder cancer cell lines were purchased from the Cell Bank of the Chinese Academy of Sciences. GBC-SD cells were cultured in RPMI-1640 medium supplemented with 10% foetal bovine serum (FBS) (cat. no. 10099141; Gibco; Thermo Fisher Scientific, Inc.), and 1% penicillin/streptomycin. NOZ cells were cultured in William’s medium supplemented with 10% foetal bovine serum (FBS) (cat. no. 10099141; Gibco; Thermo Fisher Scientific, Inc.), and 1% penicillin/streptomycin. Cells were grown at 37°C in a humidified incubator with 5% CO2.
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9

Antibody Characterization and RNAi Experiments

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The anti-p65, anti-band3, anti-p16, anti-band4.1R, anti-GPA antibodies and anti-rabbit or anti-mouse IgG were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). The anti-phosphorylated p65 (p-p65) antibody was purchased from Cell Signaling Technology (Beverly, MA, USA). The p65 inhibitor parthenolide was purchased from Santa Cruz Biotechnology. The miRNA mimics, inhibitors, non-specific control (NSC), short interfering RNA (siRNA) smart pools (for p65) and scramble control were purchased from Pharma (Shanghai, China). All-trans-retinoic acid (ATRA) was purchased from Sigma. Dasatinib was a gift from the Shanghai Institute of Blood.
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