Tse Brian W-C, Kryza Thomas, Yeh Mei-Chun, Dong Ying, Sokolowski Kamil A, Walpole Carina, Dreyer Tobias, Felber Johanna, Harris Jonathan, Magdolen Viktor, Russell Pamela J, Clements Judith A
Preclinical Imaging Facility, Translational Research Institute, Brisbane, QLD 4102, Australia.
Australian Prostate Cancer Research Centre-Queensland, Institute of Health and Biomedical Innovation, Queensland University of Technology, Translational Research Institute, Brisbane, QLD 4102, Australia.
Cancers (Basel). 2020 Nov 24;12(12):3501. doi: 10.3390/cancers12123501.
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.
最近的报告表明,激肽释放酶相关肽酶4(KLK4)在包括前列腺癌在内的许多癌症中具有重塑肿瘤微环境的作用。值得注意的是,这些研究表明KLK4具有促肿瘤发生的作用,尤其是在前列腺癌中。然而,这些主要是体外研究,迄今为止进行的体内研究有限。在此,我们采用原位接种异种移植模型来模拟原发性肿瘤的生长,并通过心内注射诱导转移扩散,以确定PC3前列腺癌细胞中过表达的KLK4的体内致瘤作用。值得注意的是,我们发现与亲本PC-3细胞相比,这些表达KLK4的细胞产生的局部肿瘤更小,转移也更少。据我们所知,这是关于KLK4,尤其是在前列腺癌中的抗肿瘤作用的首次报道。这些发现也警示了需要进行体内分析以证实体外实验数据。