Old and new serological biomarkers in melanoma: where we are in 2009

被引:22
作者
Mouawad, Roger [1 ]
Spano, Jean-Philippe [1 ]
Khayat, David [1 ]
机构
[1] Univ Paris 06, Salpetriere Hosp, AP HP, Dept Med Oncol, Paris, France
关键词
melanoma; predictive factors; prognostic factors; serological biomarkers; POLYMERASE-CHAIN-REACTION; AMERICAN-JOINT-COMMITTEE; C-REACTIVE PROTEIN; ENDOTHELIAL GROWTH-FACTOR; TYROSINASE MESSENGER-RNA; INHIBITORY-ACTIVITY MIA; SOLUBLE IL-2 RECEPTOR; ELEVATED SERUM-LEVELS; CANCER STAGE-IV; MALIGNANT-MELANOMA;
D O I
10.1097/CMR.0b013e328335a8c1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Biomarkers play an important role in the diagnosis and prognostic classification of various cancers and can be useful in monitoring the patient's clinical course of disease and response to therapy. Generally, biomarkers are proteins and their expressions are associated with malignant disease. In the majority of cases, the marker molecules are expressed by the tumour cells themselves or by the tumour microenvironment cells. Thus, most biomarkers can primarily be found in malignant tissues, but after active secretion or passive release at tumour destruction, they become detectable in body fluids such as blood. Besides morphological and histopathological biomarkers (anatomic site, type of the primary tumour, tumour size, invasion depth, vascular invasion and ulceration), an increasing variety of serological markers have been identified, providing the possibility of a more detailed diagnostic and prognostic subgrouping of tumour entities, up to and even changing existing classification systems. The goal of this review is to provide an overview of old and more recent serological biomarkers in malignant melanoma. We will first focus on confirmed and nonconfirmed serum tumour markers, followed by proteomic profiling, an innovative approach to identify new and better serological biomarkers in melanoma, and ending with the predictive factors for treatments in this pathology. Melanoma Res 20:67-76 (C) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:67 / 76
页数:10
相关论文
共 109 条
[1]   Role of RT-PCR tyrosinase detection in the monitoring of patients with advanced metastatic melanoma [J].
Abate, SO ;
Savoia, P ;
Cambieri, I ;
Salomone, B ;
Quaglino, P ;
Bernengo, MG .
MELANOMA RESEARCH, 2000, 10 (06) :545-555
[2]   Serum S-100 protein: a potentially useful prognostic marker in cutaneous melanoma [J].
Abraha, HD ;
Fuller, LC ;
DuVivier, AWP ;
Higgins, EM ;
Sherwood, RA .
BRITISH JOURNAL OF DERMATOLOGY, 1997, 137 (03) :381-385
[3]   PURIFICATION AND ANALYSIS OF GROWTH-REGULATING PROTEINS SECRETED BY A HUMAN-MELANOMA CELL-LINE [J].
APFEL, R ;
LOTTSPEICH, F ;
HOPPE, J ;
BEHL, C ;
DURR, G ;
BOGDAHN, U .
MELANOMA RESEARCH, 1992, 2 (5-6) :327-336
[4]  
Balch Charles M, 2003, Semin Surg Oncol, V21, P43, DOI 10.1002/ssu.10020
[5]   Final version of the American Joint Committee on Cancer staging system for cutaneous melanoma [J].
Balch, CM ;
Buzaid, AC ;
Soong, SJ ;
Atkins, MB ;
Cascinelli, N ;
Coit, DG ;
Fleming, ID ;
Gershenwald, JE ;
Houghton, A ;
Kirkwood, JM ;
McMasters, KM ;
Mihm, MF ;
Morton, DL ;
Reintgen, DS ;
Ross, MI ;
Sober, A ;
Thompson, JA ;
Thompson, JF .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (16) :3635-3648
[6]   POLYMERASE CHAIN-REACTION DETECTION OF CIRCULATING MELANOCYTES AS A PROGNOSTIC MARKER IN PATIENTS WITH MELANOMA [J].
BATTAYANI, Z ;
GROB, JJ ;
XERRI, L ;
NOE, C ;
ZAROUR, H ;
HOUVAENEGHEL, G ;
DELPERO, JR ;
BIRMBAUM, D ;
HASSOUN, J ;
BONERANDI, JJ .
ARCHIVES OF DERMATOLOGY, 1995, 131 (04) :443-447
[7]  
BLESCH A, 1994, CANCER RES, V54, P5695
[8]  
BOGDAHN U, 1989, CANCER RES, V49, P5358
[9]   Melanoma inhibitory activity (MIA): an important molecule in melanoma development and progression [J].
Bosserhoff, AK .
PIGMENT CELL RESEARCH, 2005, 18 (06) :411-416
[10]  
Bosserhoff AK, 1997, CANCER RES, V57, P3149