Metabolic characterization of human prostate cancer with tissue magnetic resonance spectroscopy

被引:130
作者
Cheng, LL
Burns, MA
Taylor, JL
He, WL
Halpern, EF
McDougal, WS
Wu, CL
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Pathol, Boston, MA USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Radiol, Boston, MA USA
[3] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Urol, Boston, MA USA
关键词
D O I
10.1158/0008-5472.CAN-04-4106
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diagnostic advancements for prostate cancer have so greatly increased early detections that hope abounds for improved patient outcomes. However, histopathology, which guides treatment, often subcategorizes aggressiveness insufficiently among moderately differentiated Gleason score (6 and 7) tumors (> 70% of new cases). Here, we test the diagnostic capability of prostate metabolite profiles measured with intact tissue magnetic resonance spectroscopy and the sensitivity of local prostate metabolites in predicting prostate cancer status. Prostate tissue samples (n = 199) obtained from 82 prostate cancer patients after prostatectomy were analyzed with high-resolution magic angle spinning proton magnetic resonance spectroscopy, and afterwards with quantitative pathology. Metabolite profiles obtained from principal component analysis of magnetic resonance spectroscopy were correlated with pathologic quantitative findings by using linear regression analysis and evaluated against patient pathologic statuses by using ANOVA. Paired t tests show that tissue metabolite profiles can differentiate malignant from benign samples obtained from the same patient (P < 0.005) and correlate with patient serum prostate-specific antigen levels (P < 0.006). Furthermore, metabolite profiles obtained from histologically benign tissue samples of Gleason score 6 and 7 prostates can delineate a subset of less aggressive tumors (P < 0.008) and predict tumor perineural invasion within the subset (P < 0.03). These results indicate that magnetic resonance spectroscopy metabolite profiles of biopsy tissues may help direct treatment plans by assessing prostate cancer pathologic stage and aggressiveness, which at present can be histopathologically determined only after prostatectomy.
引用
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页码:3030 / 3034
页数:5
相关论文
共 24 条
[1]   Perineural invasion is associated with increased relapse after external beam radiotherapy for men with low-risk prostate cancer and may be a marker for occult, high-grade cancer [J].
Beard, CJ ;
Chen, MH ;
Cote, K ;
Loffredo, M ;
Renshaw, AA ;
Hurwitz, M ;
D'Amico, AV .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 58 (01) :19-24
[2]   Improved biomarkers for prostate cancer: A definite need [J].
Carter, HB ;
Isaacs, WB .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (11) :813-815
[3]   Enhanced resolution of proton NMR spectra of malignant lymph nodes using magic-angle spinning [J].
Cheng, LL ;
Lean, CL ;
Bogdanova, A ;
Wright, SC ;
Ackerman, JL ;
Brady, TJ ;
Garrido, L .
MAGNETIC RESONANCE IN MEDICINE, 1996, 36 (05) :653-658
[4]   Quantitative neuropathology by high resolution magic angle spinning proton magnetic resonance spectroscopy [J].
Cheng, LL ;
Ma, MJ ;
Becerra, L ;
Ptak, T ;
Tracey, I ;
Lackner, A ;
Gonzalez, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (12) :6408-6413
[5]   Non-destructive quantitation of spermine in human prostate tissue samples using HRMAS 1H NMR spectroscopy at 9.4 T [J].
Cheng, LL ;
Wu, CL ;
Smith, MR ;
Gonzalez, RG .
FEBS LETTERS, 2001, 494 (1-2) :112-116
[6]   Stromal factors involved in prostate carcinoma metastasis to bone [J].
Cooper, CR ;
Chay, CH ;
Gendernalik, JD ;
Lee, HL ;
Bhatia, J ;
Taichman, RS ;
McCauley, LK ;
Keller, ET ;
Pienta, KJ .
CANCER, 2003, 97 (03) :739-747
[7]   Prostate cancer and health-related quality of life: A review of the literature [J].
Eton, DT ;
Lepore, SJ .
PSYCHO-ONCOLOGY, 2002, 11 (04) :307-326
[8]   Incidence, etiology, and therapy for erectile dysfunction after external beam radiotherapy for prostate cancer [J].
Incrocci, L ;
Slob, AK .
UROLOGY, 2002, 60 (01) :1-7
[9]  
Ko YJ, 2001, ONCOLOGY-NY, V15, P1113
[10]  
KO YJ, 2001, ONCOLOGY HUNTINGT, V15, P31