作者: RUI LIU , WENJIE WANG , BINGLING DAI , YANPING LIU , YANMIN ZHANG
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摘要: Taspine has been indicated to be a potential anti‑carcinogenic agent. The present study investigated the effects of TAS9, modified taspine derivative, on proliferation and migration SMMC‑7721 human liver cancer cell line. First, TAS9 growth were examined using MTT colony formation assaya. In vivo Transwell wound healing assays then performed assess inhibitory invasion migration, respectively. expression proliferation‑ migration‑associated signaling molecules was by western blot analysis. results that inhibited downregulating protein kinase Cβ (PKCβ), Akt, mammalian target rapamycin, mitogen‑activated 2, RAF c‑Jun N‑terminal kinase‑1, inhibiting suppressing matrix metalloproteinase (MMP)‑2, MMP‑9, chemokine (C‑X‑C motif) receptor 4, nuclear factor κB, p38 p53. Small interfering RNA‑mediated knockdown PKCβ in cells significantly attenuated tumor TAS9. conclusion, suggested may have cells, serve as candidate for treatment.