Abstract：
:Podoplanin (PDPN), a small transmembrane mucin-like glycoprotein, is ectopically expressed. It is also known to be linked with several aspects of tumor malignancy in some types of human tumors, including invasion, metastasis, and cancer stemness. However, there are few reports on the expression of dog PDPN (dPDPN) in canine tumors, and the association between dPDPN and tumor malignancy has not been elucidated. We identified that 11 out of 18 types of canine tumors expressed dPDPN. Furthermore, 80% of canine malignant melanoma (MM), squamous cell carcinoma, and meningioma expressed dPDPN. Moreover, the expression density of dPDPN was positively associated with the expression of the Ki67 proliferation marker. The silencing of dPDPN by siRNAs resulted in the suppression of cell migration, invasion, stem cell-like characteristics, and cell viability in canine MM cell lines. The suppression of cell viability was caused by the induction of apoptosis and G2/M phase cell cycle arrest. Overall, this study demonstrates that dPDPN is expressed in various types of canine tumors and that dPDPN silencing suppresses cell viability through apoptosis and cell cycle arrest, thus providing a novel biological role for PDPN in tumor progression.
journal_name
Cellsjournal_title
Cellsauthors
Shinada M,Kato D,Kamoto S,Yoshimoto S,Tsuboi M,Yoshitake R,Eto S,Ikeda N,Saeki K,Hashimoto Y,Takahashi Y,Chambers J,Uchida K,Kaneko MK,Fujita N,Nishimura R,Kato Y,Nakagawa Tdoi
10.3390/cells9051136subject
Has Abstractpub_date
2020-05-05 00:00:00issue
5issn
2073-4409pii
cells9051136journal_volume
9pub_type
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