COMPARISON OF MELANOMA ANTIGEN RECOGNIZED BY T-CELLS (MART-1) TO HMB-45 - ADDITIONAL EVIDENCE TO SUPPORT A COMMON LINEAGE FOR ANGIOMYOLIPOMA, LYMPHANGIOMYOMATOSIS, AND CLEAR-CELL SUGAR TUMOR
Pa. Fetsch et al., COMPARISON OF MELANOMA ANTIGEN RECOGNIZED BY T-CELLS (MART-1) TO HMB-45 - ADDITIONAL EVIDENCE TO SUPPORT A COMMON LINEAGE FOR ANGIOMYOLIPOMA, LYMPHANGIOMYOMATOSIS, AND CLEAR-CELL SUGAR TUMOR, Modern pathology, 11(8), 1998, pp. 699-703
The antibody to the melanoma antigen recognized by T cells (anti-MART-
1, clone M2-7C10) is a newly described antibody to a transmembrane pro
tein previously detected only in normal skin melanocytes, retinal tiss
ue, and malignant melanoma (MM), This antibody is the basis for ongoin
g immunotherapy protocols at the National Institutes of Health/Nationa
l Cancer Institute. HMB-45, an antibody directed against a premelanoso
me glycoprotein, although used predominantly for the diagnosis of MM,
has shown consistent staining in angiomyolipoma (AML), lymphangiomyoma
/lymphangiomyomatosis (LAM), and clear cell sugar tumor (CCST), a grou
p of tumors proposed to be related on the basis of their common periva
scular epithelioid cells, which exhibit various degrees of smooth musc
le differentiation, melanogenesis, and intracytoplasmic membrane bound
granules. To compare the immunoreactive patterns of anti-MART-1 with
those of HMB-45, we performed avidin-biotin immunoperoxidase testing o
n nonmelanocytic neoplasms (AMLs, LAMs, CCSTs) known to express HMB-45
, Microwave pretreatment was necessary for anti-MART-1 staining on par
affin-embedded material, Our results showed that all of the 10 cases o
f AML were immunoreactive for both anti-MART-1 and HMB-45; that all of
the 4 cases of LAM were positive for HMB-45, with 1 of the 4 reacting
with anti-MART-1; and that 3 of the 4 cases of CCST expressed HMB-45,
whereas 1 of the 4 was positive for anti-MART-1. Our findings lent ad
ditional support to previous studies that proposed a relationship betw
een AML, LAM, and CCST, Anti-MART-1 and HMB-45 share similar specifici
ties for these nonnelanocytic tumors, but the former seems to be a les
s sensitive marker for these lesions. In similar circumstances, anti-M
ART-1 and HMB-45 are potentially useful clinical markers.