Gm. Yousef et al., Prostase/KLK-L1 is a new member of the human kallikrein gene family, is expressed in prostate and breast tissues, and is hormonally regulated, CANCER RES, 59(17), 1999, pp. 4252-4256
By using the positional candidate gene approach, we were able to identify a
novel serine protease gene that maps to chromosome 19q13.3-q13.4. Screenin
g of expressed sequence tags allowed us to establish the expression of the
gene and delineate its genomic organization (GenBank accession no. AF135023
). We named this gene KLK-L1. Another group, by using a subtraction hybridi
zation method, cloned the same gene and named it prostase (GenBank accessio
n nos. AF113140 and AF113141). Here, we describe the precise mapping and lo
calization of the prostase/KLk-L1 gene between the known genes KLK2 (human
glandular kallikrein) and zyme (also known as protease M/neurosin). The dir
ection of transcription of prostase/KLK-L1 is the same as that of zyme but
opposite to that of KLK2 and prostate-specific antigen genes. Contrary to t
he initial impression, prostase/LK-L1 is expressed at high levels not only
in prostate tissue but also in testis, mammary gland, adrenals, uterus, thy
roid, and salivary glands. We have further demonstrated with in vitro exper
iments with the breast carcinoma cell line BT-474 that this gene is express
ed and that its expression is up-regulated by androgens and progestins. On
the basis of information on other genes that are localized in the same regi
on (prostate-specific antigen, KLK2, zyme, and normal epithelial cell speci
fic-1 gene), we speculate that prostase/KLK-L1 may be involved in the patho
genesis and/or progression of prostate, breast, and possibly other malignan
cies.