TY - JOUR
T1 - Differential expression of MART-1 in primary and metastatic melanoma lesions
AU - Kageshita, Toshiro
AU - Kawakami, Yutaka
AU - Hirai, Shunji
AU - Ono, Tomomichi
PY - 1997/1/1
Y1 - 1997/1/1
N2 - Twenty-eight primary and 29 metastatic melanoma lesions and 18 pigmented nevi lesions were analyzed by using the immunoperoxidase reaction with anti-MART-1 and anti-gp100 monoclonal antibodies (mAbs). The MART-1 was expressed in 28, 29, and 18, and gp100 was expressed in 27, 28, and eight of these lesions, respectively. Intensity and percentage of stained cells with anti-MART-1 mAb were stronger and higher than those with anti-gp100 mAb. MART-1 was expressed homogeneously in primary melanoma and pigmented nevi, whereas it was heterogeneously expressed in metastatic melanoma lesions. The level of expression of MART-1 in primary melanoma lesions did not correlate with any clinicopathologic parameters. These results suggest that anti-MART-1 mAb is a useful tool for immunohistochemical analysis of melanocytic lesions and also is useful for patient’s selection and monitoring of antigen-loss variants in clinical trials with the MART-1-based immunotherapy.
AB - Twenty-eight primary and 29 metastatic melanoma lesions and 18 pigmented nevi lesions were analyzed by using the immunoperoxidase reaction with anti-MART-1 and anti-gp100 monoclonal antibodies (mAbs). The MART-1 was expressed in 28, 29, and 18, and gp100 was expressed in 27, 28, and eight of these lesions, respectively. Intensity and percentage of stained cells with anti-MART-1 mAb were stronger and higher than those with anti-gp100 mAb. MART-1 was expressed homogeneously in primary melanoma and pigmented nevi, whereas it was heterogeneously expressed in metastatic melanoma lesions. The level of expression of MART-1 in primary melanoma lesions did not correlate with any clinicopathologic parameters. These results suggest that anti-MART-1 mAb is a useful tool for immunohistochemical analysis of melanocytic lesions and also is useful for patient’s selection and monitoring of antigen-loss variants in clinical trials with the MART-1-based immunotherapy.
KW - GP100
KW - MART-1
KW - Melanocytic tumor
UR - http://www.scopus.com/inward/record.url?scp=0030785491&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0030785491&partnerID=8YFLogxK
U2 - 10.1097/00002371-199711000-00005
DO - 10.1097/00002371-199711000-00005
M3 - Article
C2 - 9409451
AN - SCOPUS:0030785491
SN - 1053-8550
VL - 20
SP - 460
EP - 465
JO - Journal of Biological Response Modifiers
JF - Journal of Biological Response Modifiers
IS - 6
ER -