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Sk lms 1 human leiomyosarcoma cells

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The SK-LMS-1 human leiomyosarcoma cells are a cell line derived from a leiomyosarcoma, a type of soft tissue sarcoma. The cells are designed for in vitro research purposes.

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5 protocols using sk lms 1 human leiomyosarcoma cells

1

Characterization of Sarcoma Cell Lines

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HT1080 human fibrosarcoma cells and SK-LMS-1 human leiomyosarcoma cells were obtained from the American Type Culture Collection (Manassas, VA). The DDLS8817 dedifferentiated liposarcoma cell line was established from samples obtained from patients who signed informed consent forms and were confirmed by cytogenetic analysis and by DNA copy number arrays (Agilent 244 K) to harbor 12q amplification. HT1080 and SK-LMS-1 cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM), and DDLS8817 cells were maintained in DMEM-F12. All media were supplemented with 10% fetal bovine serum (FBS), penicillin (100 U/mL), streptomycin (100 μg/mL), and L-glutamine (2 mM) (“regular media”). Cancer cell lines were actively passaged for <6 months from the time that they were received, and United Kingdom Coordinating Committee on Cancer Research (UKCCCR) guidelines were followed [37 ]. Doxorubicin (RYG02) was purchased from TSZ Chem/BIOTANG Inc. (Lexington, MA). LY294002 (Cat. 440202), U0126 (Cat. 662005), and puromycin (Cat. 508838) were purchased from Calbiochem.
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2

Cultivation of Sarcoma Cell Lines

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HT1080 human fibrosarcoma cells and SK-LMS-1 human leiomyosarcoma cells were obtained from the American Type Culture Collection (ATCC). The DDLS8817 dedifferentiated liposarcoma cell line was established a tumor sample from a patient who signed informed consent and was confirmed to harbor 12q amplification by cytogenetic analysis and by DNA copy number array (Agilent 244K). HT1080 and SK-LMS-1 were maintained in Dulbecco’s Modified Eagle’s medium (DMEM), and DDLS8817 was maintained in DMEM-F12. All media were supplemented with 10% fetal bovine serum, penicillin (100 U/mL), streptomycin (100 μg/mL), and l-glutamine (2 mM) (“regular media”). Cancer cell lines were actively passaged for <6 months from the time that they were received, and United Kingdom Coordinating Committee on Cancer Research (UKCCCR) guidelines were followed28 . Doxorubicin (RYG02) and imatinib (RS029) were purchased from TSZ Chem/BIOTANG Inc. (Lexington, MA).
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3

Cultivation and Characterization of Sarcoma Cell Lines

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HT1080 human fibrosarcoma cells and SK-LMS-1 human leiomyosarcoma cells were obtained from the American Type Culture Collection (ATCC, Manassas, VA). The DDLS8817 dedifferentiated liposarcoma cell line was established from a patient sample following informed consent and were confirmed by cytogenetic analysis and by DNA copy number arrays (Agilent 244K) to harbor chromosome 12q amplification. HT1080 and SK-LMS-1 cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM), and DDLS8817 cells were maintained in DMEM-F12. All media were supplemented with 10% fetal bovine serum (FBS), penicillin (100 U/mL), streptomycin (100 μg/mL), and l-glutamine (2 mM) (hereafter termed “regular media”). Cancer cell lines were actively passaged for less than 6 months from the time that they were received, following United Kingdom Coordinating Committee on Cancer Research guidelines56 (link). Doxorubicin (RYG02) was purchased from Biotang Inc. (Lexington, MA). LY294002 (cat. 440202) and Puromycin (cat. 508838) were purchased from Calbiochem.
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4

Sarcoma Cell Lines and Reagents

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HT1080 human fibrosarcoma cells and SK-LMS-1 human leiomyosarcoma cells were obtained from the America Type Culture Collection (ATCC). MS4515 and MS5907 mouse pleomorphic undifferentiated sarcoma cell lines were derived as previously described (12 (link)). Tumor EC were harvested from HT1080 xenografts as previously described (13 (link)). Purchased reagents included anti-VEGFR2 antibody DC101 (Bio × Cell), IgG antibody (Sigma), doxorubicin (Teva Pharmaceuticals), human HIF-1α shRNA sc-35561, mouse HIF-1α shRNA sc-35562, and scramble shRNA control sc-108080 (Santa Cruz Biotechnology):.
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5

Sarcoma Cell Lines and Reagents

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HT1080 human fibrosarcoma cells and SK-LMS-1 human leiomyosarcoma cells were obtained from the America Type Culture Collection (ATCC, Manassa, VA, USA). MS4515 and MS5907 mouse undifferentiated pleomorphic sarcoma cell lines were derived from genetically engineered mouse models, which we have described previously (Kirsch et al, 2007 (link)). All sarcoma cell lines were maintained in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum, 100 U ml−1 penicillin, 100 μg ml−1 streptomycin, and L-glutamine 2 mM. Human cancer cell lines were actively passaged for <6 months from the time that they were received from ATCC, and United Kingdom Co-ordinating Committee on Cancer Research (UKCCCR) guidelines were followed (UKCCCR, 2000 (link)). Human umbilical vein endothelial cells (HUVECs) were obtained from Lonza (Basel, Switzerland) and used within eight passages. All endothelial cells were grown in EGM-2-MV media (Lonza).
The anti-VEGFR2 antibody DC101 was purchased from Bio X Cell (West Lebanon, NH, USA). Immunoglobulin G antibody was purchased from Sigma-Aldrich (St Louis, MO, USA). Doxorubicin was purchased from Teva Pharmaceuticals (Tikva, Israel). TH-302 was obtained from Threshold Pharmaceuticals (South San Francisco, CA, USA).
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