Molecular mechanism of inhibitory effects of bovine lactoferrin on the growth of oral squamous cell carcinoma

Chanbora Chea, Mutsumi Miyauchi, Toshihiro Inubushi, Nurina Febriyanti Ayuningtyas, Ajiravudh Subarnbhesaj, Phuong Thao Nguyen, Madhu Shrestha, Sivmeng Haing, Kouji Ohta, Takashi Takata

Research output: Contribution to journalArticlepeer-review

36 Citations (Scopus)

Abstract

Background Lactoferrin (LF), a member of the transferrin family, recently has been demonstrated to have anticancer effects on various cancers including oral squamous cell carcinoma (OSCC). However, little is known about the underlying mechanisms of its effects on OSCC. Therefore, we aimed to investigate the mechanism of the suppressive effects of bovine LF (bLF) on the growth of OSCC cells. Methods In the current study, HSC2, HSC3, HSC4 and normal human oral keratinocytes (RT7) cell lines were tested with bLF 1, 10, and 100 μg/ml. The effects and detail mechanisms of bLF on proliferation and apoptosis of cells were investigated using flow cytometry and western blotting. Results We found that bLF (1, 10, and 100 μg/ml) induced activation of p53, a tumor suppressor gene, is associated with the induction of cell cycle arrest in G1/S phase and apoptosis in OSCC. Moreover, bLF downregulated the phosphorylation of Akt and activated suppressor of cytokine signaling 3 (SOCS3), thereby attenuating multiple signaling pathways including mTOR/S6K and JAK/STAT3. Interestingly, we revealed that bLF exerted its effect selectively against HSC3 but not on RT7 via different effects on the phosphorylation status of NF-κB and Akt. Conclusion This is the first report showing that bLF selectively suppresses proliferation through mTOR/ S6K and JAK/STAT3 pathways and induction of apoptosis in OSCC. This study provides important new findings, which might be useful in the prevention and treatment of OSCC.

Original languageEnglish
Article numbere0191683
JournalPLoS ONE
Volume13
Issue number1
DOIs
Publication statusPublished - Jan 2018
Externally publishedYes

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