Surfaced-enhanced laser desorption/ionization time-of-flight (SELDI-TOF) differentiation of serum protein profiles of BRCA-1 and sporadic breast cancer

被引:86
作者
Becker, S
Cazares, LH
Watson, P
Lynch, H
Semmes, OJ
Drake, RR
Laronga, C
机构
[1] Eastern Virginia Med Sch, Dept Surg, Norfolk, VA 23507 USA
[2] Eastern Virginia Med Sch, Dept Microbiol, Norfolk, VA 23507 USA
[3] Eastern Virginia Med Sch, Dept Mol & Cell Biol, Norfolk, VA 23507 USA
[4] Virginia Prostate Ctr, Norfolk, VA USA
[5] Creighton Univ, Dept Prevent Med, Omaha, NE 68178 USA
关键词
BRCA-1; breast cancer; protein profiling; serum;
D O I
10.1245/ASO.2004.03.557
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: BRCA-l mutations predispose women to early onset breast cancer, but similar to20% never develop cancer. Surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF MS) profiling can differentiate protein signatures of cancer and normal subjects. Our objective was to distinguish women with BRCA-1 mutations who developed breast cancer (BRCA-1 Ca) from those who did not (Carrier), normal volunteers (NL), and women with sporadic breast cancer (SBC), using SELDI-TOF. Methods: Baseline serum specimens were obtained from women with BRCA-1 mutations without cancer, SBC, and NL. BRCA-1 women were later divided into two cohorts, pending cancer development. The sera were spotted onto protein chips for SELDI-TOF analysis and analyzed with classification algorithm software. Results: BRCA-1 Ca patients (n = 15) developed cancer within 3 years of baseline, whileBRCA-1 carriers (n = 15) were cancer-free in 7 years of follow-up. SELDI-TOF analysis revealed differentially expressed proteins (P < .05) between BRCA-1 Ca, Carrier, and SBC patients (n = 16), such that 13/15 BRCA-1 Ca vs. Carrier women were correctly identified (sensitivity/specificity of 87%/87%) and 14/15 BRCA-1 Ca vs. SBC patients were correctly identified (sensitivity/ specificity 94%/100%). Profiles of Carriers resembled NL profiles (n = 16). Conclusions: SELDI-TOF protein profiles from this small pilot study distinguished between women with BRCA-1 Ca, Carriers, and women with SBC. Whether BRCA-1 Ca represents earlier detection of occult cancer or other risk factors is unknown. Follow-up studies with larger numbers and longer follow-up are required to validate these findings but may allow more timely prophylactic or therapeutic strategies.
引用
收藏
页码:907 / 914
页数:8
相关论文
共 14 条
  • [1] Adam BL, 2002, CANCER RES, V62, P3609
  • [2] Cazares LH, 2002, CLIN CANCER RES, V8, P2541
  • [3] LINKAGE OF EARLY-ONSET FAMILIAL BREAST-CANCER TO CHROMOSOME-17Q21
    HALL, JM
    LEE, MK
    NEWMAN, B
    MORROW, JE
    ANDERSON, LA
    HUEY, B
    KING, MC
    [J]. SCIENCE, 1990, 250 (4988) : 1684 - 1689
  • [4] Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
    King, MC
    Marks, JH
    Mandell, JB
    [J]. SCIENCE, 2003, 302 (5645) : 643 - 646
  • [5] Lakhani SR, 1997, LANCET, V349, P1505
  • [6] Li JN, 2002, CLIN CHEM, V48, P1296
  • [7] Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation.
    Meijers-Heijboer, H
    van Geel, B
    van Putten, WLJ
    Henzen-Logmans, SC
    Seynaeve, C
    Menke-Pluymers, MBE
    Bartels, CCM
    Verhoog, LC
    van den Ouweland, AMW
    Niermeijer, MF
    Brekelmans, CTM
    Klijn, JGM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (03) : 159 - 164
  • [8] Use of proteomic patterns in serum to identify ovarian cancer
    Petricoin, EF
    Ardekani, AM
    Hitt, BA
    Levine, PJ
    Fusaro, VA
    Steinberg, SM
    Mills, GB
    Simone, C
    Fishman, DA
    Kohn, EC
    Liotta, LA
    [J]. LANCET, 2002, 359 (9306) : 572 - 577
  • [10] Long-term psychological impact of carrying a BRCA1/2 mutation and prophylactic surgery: A 5-year follow-up study
    van Oostrom, I
    Meijers-Heijboer, H
    Ladder, LN
    Duivenvoorden, HJ
    van Goal, AR
    Seynaeve, C
    van der Meer, CA
    Klijn, JGM
    van Geel, BN
    Burger, CW
    Wladimiroff, JW
    Tibben, A
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (20) : 3867 - 3874