| Literature DB >> 33255452 |
Brian W-C Tse1,2,3, Thomas Kryza2,3,4, Mei-Chun Yeh2,3, Ying Dong2,3, Kamil A Sokolowski1, Carina Walpole2,3,4, Tobias Dreyer5, Johanna Felber5, Jonathan Harris3, Viktor Magdolen5, Pamela J Russell2,3, Judith A Clements2,3.
Abstract
Recent reports have suggested the role of kallikrein-related peptidase 4 (KLK4) to be that of remodeling the tumor microenvironment in many cancers, including prostate cancer. Notably, these studies have suggested a pro-tumorigenic role for KLK4, especially in prostate cancer. However, these have been primarily in vitro studies, with limited in vivo studies performed to date. Herein, we employed an orthotopic inoculation xenograft model to mimic the growth of primary tumors, and an intracardiac injection to induce metastatic dissemination to determine the in vivo tumorigenic effects of KLK4 overexpressed in PC3 prostate cancer cells. Notably, we found that these KLK4-expressing cells gave rise to smaller localized tumors and decreased metastases than the parent PC-3 cells. To our knowledge, this is the first report of an anti-tumorigenic effect of KLK4, particularly in prostate cancer. These findings also provide a cautionary tale of the need for in vivo analyses to substantiate in vitro experimental data.Entities:
Keywords: KLK4; imaging; kallikrein-related peptidase 4; metastasis; prostate cancer; tumor xenografts
Year: 2020 PMID: 33255452 PMCID: PMC7761350 DOI: 10.3390/cancers12123501
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639