Klk4 induces anti-tumor effects in human xenograft mouse models of orthotopic and metastatic prostate cancer

Brian W.C. Tse, Thomas Kryza, Mei Chun Yeh, Ying Dong, Kamil A. Sokolowski, Carina Walpole, Tobias Dreyer, Johanna Felber, Jonathan Harris, Viktor Magdolen, Pamela J. Russell, Judith A. Clements

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

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.

Original languageEnglish
Article number3501
Pages (from-to)1-15
Number of pages15
JournalCancers
Volume12
Issue number12
DOIs
StatePublished - Dec 2020

Keywords

  • Imaging
  • KLK4
  • Kallikrein-related peptidase 4
  • Metastasis
  • Prostate cancer
  • Tumor xenografts

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