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Apoptotic effect and mechanisms of AHPN on human skin malignant melanoma cell A375 被引量:2

Apoptotic effect and mechanisms of AHPN on human skin malignant melanoma cell A375
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摘要 Objective: To study apoptotic effects of synthetic retinoic acid 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic acid(AHPN) on human skin malignant melanoma A375 cells in comparison with the natural ligand all-trans-retinoic acid(ATRA) in vitro and the mechanisms related to the actions of AHPN. Methods:MTT assay was used to determine the anti-proliferative effects of AHPN and ATRA on A375 cells. Flow cytometry was performed to investigate the influence of AHPN and ATRA on cell cycle and cell apoptosis. In addition, transfection and luciferase activity assays were employed to explore the mechanisms of how AHPN executes its proapoptotic function. Results:Firstly, AHPN promoted apoptosis and GI arrest in A375 cells compared with ATRA. Secondly, the activity of NF-K B in A375 cells treated with AHPN increased 2-3 times compared with solvent DMSO treatment. Conclusion:AHPN, in comparison with ATRA, is a more effective alternative for therapy of malignant melanoma. The potentially proapoptotic function of AHPN requires activation of NF-K B. Objective: To study apoptotic effects of synthetic retinoic acid 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic acid(AHPN) on human skin malignant melanoma A375 cells in comparison with the natural ligand all-trans-retinoic acid(ATRA) in vitro and the mechanisms related to the actions of AHPN. Methods:MTT assay was used to determine the anti-proliferative effects of AHPN and ATRA on A375 cells. Flow cytometry was performed to investigate the influence of AHPN and ATRA on cell cycle and cell apoptosis. In addition, transfection and luciferase activity assays were employed to explore the mechanisms of how AHPN executes its proapoptotic function. Results:Firstly, AHPN promoted apoptosis and GI arrest in A375 cells compared with ATRA. Secondly, the activity of NF-K B in A375 cells treated with AHPN increased 2-3 times compared with solvent DMSO treatment. Conclusion:AHPN, in comparison with ATRA, is a more effective alternative for therapy of malignant melanoma. The potentially proapoptotic function of AHPN requires activation of NF-K B.
出处 《Journal of Nanjing Medical University》 2008年第1期18-22,共5页 南京医科大学学报(英文版)
基金 National Natural Science Funds(No30371295)
关键词 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic acid(AHPN) ATRA A375 cell line apoptosis NF-K B 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic acid(AHPN) ATRA A375 cell line apoptosis NF-K B
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  • 1N. Hail,H. J. Kim,R. Lotan.Mechanisms of fenretinide-induced apoptosis[J].Apoptosis.2006(10) 被引量:1
  • 2Robert A. Nagourney MD.Ex vivo programmed cell death and the prediction of response to chemotherapy[J].Current Treatment Options in Oncology.2006(2) 被引量:1
  • 3Fecher LA,Cummings SD,Keefe MJ,Alani RM.Toward a mo-lecular classification of melanoma[].Journal of Clinical Oncology.2007 被引量:1
  • 4Postovit LM,Seftor EA,Seftor REB,Hendrix MJC.Targeting nodal in malignant melanoma cells[].Expert Opinion on Therapeutic Targets.2007 被引量:1
  • 5Markovic SN,Erickson LA,Rao RD,Weenig RH,Pockaj BA,Bardia A,et al.Malignant melanoma in the 21st century part 2: staging,prognosis,and treatment[].Mayo Clinic Proceedings.2007 被引量:1
  • 6La Porta CA.Drug resistance in melanoma: new perspectives[].Cur-rent Medicinal Chemistry.2007 被引量:1
  • 7Zanardi S,Serrano D,Argusti A,Barile M,Puntoni M,Decensi A.Clinical trials with retinoids for breast cancer chemoprevention[].Endocrine Related Cancer.2006 被引量:1
  • 8Garattini E,Gianni M,Terao M.Retinoids as differentiating agents in oncology: a network of interactions with intracellular pathways as the basis for rational therapeutic combinations[].Current Phar-maceutical Design.2007 被引量:1
  • 9Zhang C,Duvic M.Treatment of cutaneous T-cell lymphoma with retinoids[].Dermatologic Therapy.2006 被引量:1
  • 10Hail N,Kim H,Lotan R.Mechanisms of fenretinide-induced apoptosis[].Apoptosis.2006 被引量:1

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