Poly(adenosine diphosphate-ribose) polymerase 1 expression in malignant melanomas from photoexposed areas of the head and neck region

被引:79
作者
Staibano, S [1 ]
Pepe, S
Lo Muzio, L
Somma, P
Mascolo, M
Argenziano, G
Scalvenzi, M
Salvatore, G
Fabbrocini, G
Molea, G
Bianco, AR
Carlomagno, C
De Rosa, G
机构
[1] Univ Naples Federico II, Dept Biomorphol & Funct Sci, Pathol Sect, I-80127 Naples, Italy
[2] Univ Naples Federico II, Dept Mol & Clin Endocrinol & Oncol, I-80127 Naples, Italy
[3] Univ Naples Federico II, Dept Dermatol, I-80127 Naples, Italy
[4] SUN Univ, Dept Dermatol, I-80127 Naples, Italy
[5] Univ Naples Federico II, Cooperat Melanova Grp, I-80127 Naples, Italy
[6] Univ Naples Federico II, Dept Plast Surg, I-80127 Naples, Italy
[7] Univ Naples Federico II, Dept Med, I-80127 Naples, Italy
关键词
cutaneous melanoma; PARP-l; prognosis;
D O I
10.1016/j.humpath.2005.04.017
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The family of the of adenosine diphosphate-ribose) polymerase (PARP) proteins is directly involved in genomic stability, DNA repair, and apoptosis by DNA damage. In this study, we evaluated the role of PARP-1 in melanoma and its prognostic importance. We studied by immunohistochemistry and Western blot analysis PARP-I expression in a selected series of 80 primary melanoma of the head and neck region. The results were correlated with tumor thickness and patient's outcome. A follow-up of at least 3 years was available. Fifteen cases of benign melanocytic nevi were used as controls. Normal melanocytes showed only scattered, focal nuclear positivity and were considered as negative for PARP-1 expression by immunohistochemistry (score, 0). Thirty cases of melanoma (37.5%) showed nuclear expression of PARP-1 in both radial and vertical growth phases. Western blot analysis showed the presence of a high signal for full-length PARP-1 only in the cases with high immunohistochemical (nuclear) expression of protein (score, ++/+++) in both radial and vertical growth phase. A significant correlation was present between PARP-1 expression in vertical growth phase and the thickness of tumor lesion (P = .014); all but one tumor measuring less than 0.75 mm showed no or low PARP-1 expression. No correlation was found between PARP-1 expression in radial growth phase and tumor thickness (P = .38, data not shown). These data suggest that PARP-1 overexpression is a potential novel molecular marker of aggressive cutaneous malignant melanoma and a direct correlation between PARP-1-mediated inhibition of the apoptosis and biologic behavior of cutaneous malignant melanoma. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:724 / 731
页数:8
相关论文
共 42 条
[1]   CASE-CONTROL STUDY OF MELANOCYTIC NEVI ON THE BUTTOCKS IN ATYPICAL MOLE SYNDROME - ROLE OF SOLAR-RADIATION IN THE PATHOGENESIS OF ATYPICAL MOLES [J].
ABADIR, MC ;
MARGHOOB, AA ;
SLADE, J ;
SALOPEK, TG ;
YADAV, S ;
KOPF, AW .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1995, 33 (01) :31-36
[2]   p53 and DNA damage-inducible expression of the xeroderma pigmentosum group C gene [J].
Adimoolam, S ;
Ford, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12985-12990
[3]   CUTANEOUS MALIGNANT-MELANOMA AND EXPOSURE TO SUNLAMPS OR SUNBEDS - AN EORTC MULTICENTER CASE-CONTROL STUDY IN BELGIUM, FRANCE AND GERMANY [J].
AUTIER, P ;
DORE, JF ;
LEJEUNE, F ;
KOELMEL, KF ;
GEFFELER, O ;
HILLE, P ;
CESARINI, JP ;
LIENARD, D ;
LIABEUF, A ;
JOARLETTE, M ;
CHEMALY, P ;
HAKIM, K ;
KOELN, A ;
KLEEBERG, UR .
INTERNATIONAL JOURNAL OF CANCER, 1994, 58 (06) :809-813
[4]   Sunburn, sunscreens, and phenotypes: some risk factors for cutaneous melanoma in southern Brazil [J].
Bakos, L ;
Wagner, M ;
Bakos, RM ;
Leite, CSM ;
Sperhacke, CL ;
Dzekaniak, KS ;
Gleisner, ALM .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2002, 41 (09) :557-562
[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]  
BALCH CM, 2002, AJCC CANC STAGING MA, P209
[7]   DNA repair/pro-apoptotic dual-role proteins in five major DNA repair pathways: fail-safe protection against carcinogenesis [J].
Bernstein, C ;
Bernstein, H ;
Payne, CM ;
Garewal, H .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2002, 511 (02) :145-178
[8]   BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH [J].
BOISE, LH ;
GONZALEZGARCIA, M ;
POSTEMA, CE ;
DING, LY ;
LINDSTEN, T ;
TURKA, LA ;
MAO, XH ;
NUNEZ, G ;
THOMPSON, CB .
CELL, 1993, 74 (04) :597-608
[9]  
Böni R, 2002, NEUROENDOCRINOL LETT, V23, P48
[10]   SEASONAL-VARIATION IN FREQUENCY OF DIAGNOSIS OF CUTANEOUS MALIGNANT-MELANOMA [J].
BRAUN, MM ;
TUCKER, MA ;
DEVESA, SS ;
HOOVER, RN .
MELANOMA RESEARCH, 1994, 4 (04) :235-241