INCREASED EPIDERMAL GROWTH-FACTOR RECEPTORS IN MELANOCYTIC LESIONS

被引:34
作者
ELLIS, DL
KING, LE
NANNEY, LB
机构
[1] DEPT VET AFFAIRS,NASHVILLE,TN
[2] VANDERBILT UNIV,DEPT MED,DIV DERMATOL,NASHVILLE,TN 37240
[3] VANDERBILT UNIV,DEPT CELL BIOL,NASHVILLE,TN 37240
[4] VANDERBILT UNIV,DEPT PLAST SURG,NASHVILLE,TN 37240
关键词
D O I
10.1016/0190-9622(92)70219-6
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Epidermal growth factor receptors (EGF/R) have been reported to be absent in melanomas or, in contrast, to be markers for potential malignancy in melanocytic lesions. Objective: Our purpose was to evaluate the literature discrepancies regarding the presence of EGF/R in melanocytic lesions and to determine whether EGF/R presence correlates with the potential for malignancy of melanocytic lesions. Methods: An EGF/R-specific polyclonal antibody was used to study melanomas, dysplastic nevi, congenital nevi, and nevocellular nevi. Results: All melanocytic cell types (nevus and melanoma cells) in the lesions studied had immunoreactive EGF/R. EGF/R immunoreactivity was also observed throughout the epidermal basal to granular cell layers overlying the melanocytic lesions, although dermal fibroblasts were negative. Conclusion: The pattern of increased immunoreactive EGF/R in both benign and malignant nevocellular lesions suggests that although EGF/R are not a specific marker of potential malignancy in melanocytic lesions, they may mediate or coordinate growth of keratinocytes and nevus cells.
引用
收藏
页码:539 / 546
页数:8
相关论文
共 18 条
[1]   EPIDERMAL GROWTH-FACTOR RECEPTORS IN DIFFERENT SKIN TUMORS [J].
BAUKNECHT, T ;
GROSS, G ;
HAGEDORN, M .
DERMATOLOGICA, 1985, 171 (01) :16-20
[2]  
CARPENTER G, 1990, J BIOL CHEM, V265, P7709
[3]   EPIDERMAL GROWTH-FACTOR REGULATES THE EXPRESSION OF ITS OWN RECEPTOR [J].
CLARK, AJL ;
ISHII, S ;
RICHERT, N ;
MERLINO, GT ;
PASTAN, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (24) :8374-8378
[4]  
ELDER DE, 1989, CANCER RES, V49, P5091
[5]   THE DYSPLASTIC NEVUS SYNDROME [J].
ELDER, DE ;
GREEN, MH ;
GUERRY, D ;
KRAEMER, KH ;
CLARK, WH .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1982, 4 (05) :455-460
[6]  
ELIAS JM, 1990, IMMUNOHISTOPATHOLOGY, P38
[7]   MELANOMA, GROWTH-FACTORS, ACANTHOSIS NIGRICANS, THE SIGN OF LESER-TRELAT, AND MULTIPLE ACROCHORDONS - A POSSIBLE ROLE FOR ALPHA-TRANSFORMING GROWTH-FACTOR IN CUTANEOUS PARA-NEOPLASTIC SYNDROMES [J].
ELLIS, DL ;
KAFKA, SP ;
CHOW, JC ;
NANNEY, LB ;
INMAN, WH ;
MCCADDEN, ME ;
KING, LE .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (25) :1582-1587
[8]   INCREASED EPIDERMAL GROWTH-FACTOR RECEPTORS IN SEBORRHEIC KERATOSES AND ACROCHORDONS OF PATIENTS WITH THE DYSPLASTIC NEVUS SYNDROME [J].
ELLIS, DL ;
NANNEY, LB ;
KING, LE .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1990, 23 (06) :1070-1077
[9]   REGULATION OF PHOSPHOLIPASE-C-GAMMA-1 BY PROFILIN AND TYROSINE PHOSPHORYLATION [J].
GOLDSCHMIDTCLERMONT, PJ ;
KIM, JW ;
MACHESKY, LM ;
RHEE, SG ;
POLLARD, TD .
SCIENCE, 1991, 251 (4998) :1231-1233
[10]  
KUDLOW JE, 1986, J BIOL CHEM, V261, P4134