期刊文献+

GP100与GPNMB分子水平在黑素瘤预后中的意义

Evaluation of GP100 and GPNMB on the prognosis of patients with melanoma
下载PDF
导出
摘要 目的:探讨可溶性分子GP100和GPNMB在黑素瘤诊断及预后中的意义。方法:采用ELISA检测分析健康对照组、良性黑素瘤组及黑素瘤组患者血清中GP100与GPNMB的分子水平变化。结果:良性黑素瘤组患者血清中GP100平均含量为(4.83±1.13)ng/mL,是健康对照组的4.1倍(P<0.05);而恶性黑素瘤组为(13.82±2.19)ng/mL,是健康对照组的12倍(P<0.01)。良性黑素瘤组患者血清中GPNMB的平均含量为(2.56±0.84)ng/mL,是健康对照组的2.7倍(P<0.05);而恶性黑素瘤组平均含量为(15.34±2.52)ng/mL,是健康对照组的16.68倍(P<0.01)。GP100与GPNMB的水平与黑素瘤恶性程度呈正相关。当恶性黑素瘤患者GP100的含量≥5.43 ng/mL,平均生存周期为11个月;而<5.34ng/mL,平均生存周期为35个月,两者之间差异有统计学意义(P<0.01),表明可溶性GP100含量与黑素瘤患者预后呈负相关(P<0.05)。GPNMB含量≥2.72 ng/mL时,恶性黑素瘤患者预后平均存活时间约为11.3个月;<2.72 ng/mL时,预后平均生存期为36个月,两者之间差异有统计学意义(P<0.01)。GPNMB与黑素瘤患者预后呈负相关。结论:血清中GP100及GPNMB的含量是影响黑素瘤患者预后的因素之一,有助于黑素瘤患者的预后评估。 Objective:To explore the correlation between the serum levels of GP100 and GPNMB and the prognosis of human melanoma.Methods:The serum levels of GP100 and GPNMB were quantitatively using ELISA in healthy control,melanoma benign or melanoma patients.Resuits:The G P100 concentrations of begin melanoma and melanoma patients were (4.83 ±1.13) ng/mL (4.1 times versus control)and 13.82 ± 2.19 ng/mL (12 times versus control),respectively.Whereas the levels of GPNMB were (2.56 ± 0.84) ng/mL (2.7 times versus control) and (15.34 ± 2.52) ng/mL (16.68 times versus control)in begin and melanoma patients,separately.In addition,for 97 begin melanoma patients; increased serum levels of GP100 and GPNMB at diagnosis were associated with a poor prognosis.Patients with GP100 concentrations below or above 5.43 ng/mL had obviously different survival times (median > 35 months or <11 months,respectively).Simultaneously,patients with GPNMB levels up or down 2.72 ng/mL still exhibited a poor prognosis (median >36months or <11.3 months,respectively).Conclusion:The levels of GP100 and GPNMB play important roles in the pathogenesis of melanoma and exert crucial function in the prognosis of melanoma patients.Therefore,both of these two molecules will be new independent prognostic indicators.
出处 《中国现代普通外科进展》 CAS 2013年第10期786-788,805,共4页 Chinese Journal of Current Advances in General Surgery
关键词 黑素瘤 GP100 GPNMB 预后 Melanoma GP100 GPNMB Prognosis
  • 相关文献

参考文献14

  • 1Thompson JF,Scolyer RA,Kefford RF.Cutaneous melanoma[J].The Lancet,2005,365 (9460):687-701.
  • 2韩睿,程浩,朱可建.恶性黑素瘤血清学预后标记研究进展[J].实用肿瘤杂志,2007,22(4):371-373. 被引量:1
  • 3Loftus SK,Antonellis A,Matera I,et al.Gpnmb is a melanoblastexpressed,MITF-dependent gene[J].Pigment cell & melanoma research,2009,22(1):99-110.
  • 4Deichmann M,Benner A,Bock M,et al.S100-Beta,melanoma-inhibiting activity,and lactate dehydrogenase discriminate progressive from nonprogressive American Joint Committee on Cancer stage Ⅳ melanoma[J].Journal of clinical oncology,1999,17(6):1891-1891.
  • 5Berson JF,Harper DC,Tenza D,et al.Pmel17 initiates premelanosome morphogenesis within multivesicular bodies[J].Molecular biology of the cell,2001,12(11):3451-3464.
  • 6李昂,刘荣军,林怡,熊思东,储以微.人黑色素肿瘤相关抗原gp100质粒诱导特异性抗小鼠黑色素瘤的免疫保护效应[J].中华微生物学和免疫学杂志,2006,26(4):334-338. 被引量:2
  • 7Rosenberg SA.Cancer vaccines based on the identification of genes encoding cancer regression antigens[J].Immunology today,1997,18(4):175-182.
  • 8Tomihari M,Hwang SH,Chung JS,et al.Gpnmb is a melanosomeassociated glycoprotein that contributes to melanocyte/keratinocyte adhesion in a RGD-dependent fashion[.J].Exp Dermatol,2009,18(7):586-595.
  • 9Schwartzentruber DJ,Lawson DH,Richards JM,et al.GP100 peptide vaccine and interleukin-2 in patients with advanced melanoma[J].N Engl J Med,2011,364(22):2119-2127.
  • 10Rosenberg SA,Yang JC,Sherry RM,et al.Inability to immunize patients with metastatic melanoma using plasmid DNA encoding the gp100 melanoma-melanocyte antigen[J].Human gene therapy,2003,14(8):709-714.

二级参考文献30

  • 1Overwijk WW,Tsung A,Irvine KR,et al.gp100/pmel 17 is a murine umor rejection antigen:induction of "self"-reactive,tumoricidal T cells using high-affinity,altered peptide ligand.J Exp Med,1998,188:277-286.
  • 2Disis ML.Immunologic targets for breast cancer.Breast Dis,2002,15:83-90.
  • 3Hartmann TB,Bazhin AV,Schadendorf D,et al.SEREX identification of new tumor antigens linked to melanoma-associated retinopathy.Int J Cancer,2005,114(1):88-93.
  • 4Benlalam H,Linard B,Guilloux Y,et al.Identification of five new HLA-B * 3501-restricted epitopes derived from common melanoma-associated antigens,spontaneously recognized by tumor-infiltrating lymphocytes.J Immunol,2003,171(11):6283-6289.
  • 5Wei YQ.Immunotherapy of tumors with vaccines based on xenogeneic homologous molecules.Anticancer Drugs,2002,13 (3):229-235.
  • 6Gallo P,Dharmapuri S,Nuzzo M,et al.Xenogeneic immunization in mice using HER2 DNA delivered by an adenoviral vector.Int J Cancer,2005,113(1):67-77.
  • 7Wei YQ,WangQR,ZhaoX,etal.Immunotherapy of tumors with xenogeneic endothelial cells as a vaccine.Nat Med,2000,6:1160-1166.
  • 8Rosenberg SA.Cancer vaccines based on the identification of genes encoding cancer regression antigens.Immunol Today,1997,18:175-182.
  • 9Zhai Y,Yang JC,Spiess P,et al.Cloning and characterization of the genes encoding the mmrine homologues of the melanoma antigens MART1 and gp100.J Immunother,1997,20:15-25.
  • 10LecoeurH,FevrierM,GarciaS,etal.A novel flow cytometric assay for quantitation and multiparametric characterization of cell-mediated cytotoxicity.J Immunol Methods,2001,253:177-187.

共引文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部