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Cited by 675

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The New Human Tissue Kallikrein Gene Family: Structure, Function, and Association to Disease*

Yousef, George M., Diamandis, Eleftherios P.·2001·Endocrine Reviews

Abstract

The human tissue kallikrein gene family was, until recently, thought to consist of only three genes. Two of these human kallikreins, prostate-specific antigen and human glandular kallikrein 2, are currently used as valuable biomarkers of prostatic carcinoma. More recently, new kallikrein-like genes have been discovered. It is now clear that the human tissue kallikrein gene family contains at least 15 genes. All genes share important similarities, including mapping at the same chromosomal locus (19q13.4), significant homology at both the nucleotide and protein level, and similar genomic organization. All genes encode for putative serine proteases and most of them are regulated by steroid hormones. Recent data suggest that at least a few of these kallikrein genes are connected to malignancy. In this review, we summarize the recently accumulated knowledge on the human tissue kallikrein gene family, including gene and protein structure, predicted enzymatic activities, tissue expression, hormonal regulation, and alternative splicing. We further describe the reported associations of the human kallikreins with various human diseases and identify future avenues for research.

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Metadata

Authors
Yousef, G. M., & Diamandis, E. P.
Venue
Endocrine Reviews
Published
2001-04-01
Volume
22
Issue
2
Pages
184-204
ISSN
  • 0163-769X (ISSN-L)
  • 1945-7189
OpenAlex
W1972581901
Cited by
675
References
1
FWCI
16.14
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The New Human Tissue Kallikrein Gene Family: Structure, Function, and Association to Disease*. https://app.cochat.ai/papers/10.1210/edrv.22.2.0424
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Yousef, G. M., & Diamandis, E. P. (2001). The New Human Tissue Kallikrein Gene Family: Structure, Function, and Association to Disease*. Endocrine Reviews. https://doi.org/10.1210/edrv.22.2.0424

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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