Sufang Liu
Central South University
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Featured researches published by Sufang Liu.
FEBS Letters | 2005
Mao Ye; Ji-Kai Liu; Zhongxin Lu; Yan Zhao; Sufang Liu; Lili Li; Ming Tan; Xinxian Weng; Wei Li; Ya Cao
Grifolin is a natural biologically active substance isolated from the fresh fruiting bodies of the mushroom Albatrellus confluens. Here, for the first time, we describe a novel activity of grifolin, namely its ability to inhibit the growth of tumor cells by the induction of apoptosis. Grifolin strongly inhibited the growth of tumor cell lines: CNE1, HeLa, MCF7, SW480, K562, Raji and B95‐8. Analysis of acridine orange (AO)/ethidium bromide (EB) staining and flow cytometry showed that grifolin possessed apoptosis induction activity to CNE1, HeLa, MCF7 and SW480. Furthermore, the cytochrome c release from mitochondria was detected by confocal microscopy in CNE1 cells after a 12 h treatment with grifolin. The increase of caspase‐8, 9, 3 activities revealed that caspase was a key mediator of the apoptotic pathway induced by grifolin, and the underexpression of Bcl‐2 and up‐regulation of Bax resulted in the increase of Bax: Bcl‐2 ratio, suggesting that Bcl‐2 family involved in the control of apoptosis. Owing to the combination of the significant antitumor activity by inducing apoptosis and natural abundance of the compound, grifolin holds the promise of being an interesting antitumor agent that deserves further laboratory and in vivo exploration.
Carcinogenesis | 2013
Sufang Liu; Hongde Li; Lin Chen; Lifang Yang; Lili Li; Yongguang Tao; Wei Li; Zijian Li; Haidan Liu; Min Tang; Ann M. Bode; Zigang Dong; Ya Cao
Epstein-Barr virus (EBV) reactivation into the lytic cycle plays certain roles in the development of EBV-associated diseases, including nasopharyngeal carcinoma and lymphoma. In this study, we investigated the effects of the tea polyphenol (-)-epigallocatechin-3-gallate (EGCG) on EBV spontaneous lytic infection and the mechanism(s) involved in EBV-positive cells. We found that EGCG could effectively inhibit the constitutive lytic infection of EBV at the DNA, gene transcription and protein levels by decreasing the phosphorylation and activation of extracellular signal-regulated kinase 1/2 (ERK1/2) and Akt. By using cellular signaling pathway-specific inhibitors, we also explored the signaling mechanisms underlying the inhibitory effects of EGCG on EBV spontaneous lytic infection in cell models. Results show that specific inhibitors of Mitogen-Activated Protein Kinase Kinase (MEK) (PD98059) and phosphatidylinositol 3-kinase [PI3-K (LY294002)] markedly downregulated gene transcription and expression of BZLF1 and BMRF1 indicating that the MEK/ERK1/2 and PI3-K/Akt pathways are involved in the EBV spontaneous lytic cycle cascade. Therefore, one of the mechanisms by which EGCG inhibits EBV spontaneous lytic infection appears to involve the suppression of the activation of MEK/ERK1/2 and PI3-K/Akt signaling.
International Journal of Cancer | 2009
Xuechi Lin; Sufang Liu; Xiangjian Luo; Xiaoqian Ma; Lili Guo; Lili Li; Zijian Li; Yongguang Tao; Ya Cao
Oncoprotein 18/stathmin (Op18/stathmin) plays a crucial role in maintaining cell biological characteristics by regulating microtubule dynamics, especially entry into mitosis; phosphorylated Op18/stathmin promotes microtubule polymerization to form the mitotic spindle, which is essential for chromosome segregation and cell division. Cdc2 is a critical kinase in starting M phase events in cell‐cycle progression and is a positive regulator of the cell cycle. Latent membrane protein 1 (LMP1) is an Epstein‐Barr virus (EBV)‐encoded oncogenic protein that is able to induce carcinogenesis via various signaling pathways. This study focused on regulation by LMP1 of Op18/stathmin signaling in nasopharyngeal carcinoma (NPC) cells and showed that LMP1 regulates Op18/stathmin signaling through cdc2 mediation, LMP1 upregulates cdc2 kinase activity, and Op18/stathmin phosphorylation promotes the interaction of cdc2 with Op18/stathmin and microtubule polymerization during mitosis, and inhibition of LMP1 expression attenuates the interaction of cdc2 and Op18/stathmin and promotes microtubule depolymerization. These results reveal a new pathway via which LMP1 regulates Op18/stathmin signaling by cdc2 mediation; this new signaling pathway not only perfects the LMP1 regulation network but also elucidates the molecular mechanism of LMP1 that leads to carcinogenesis.
Molecular Carcinogenesis | 2008
Wei Luo; Guangrong Yan; Lili Li; Zhenlian Wang; Haidan Liu; Shanghui Zhou; Sufang Liu; Min Tang; Wei Yi; Zigang Dong; Ya Cao
We have previously elucidated that Epstein–Barr‐virus‐encoded latent membrane protein 1 (LMP1) can increase the serine phosphorylation level of annexin A2 by activating the protein kinase C (PKC) signaling pathway and that LMP1 induces the nuclear entry of annexin A2 in an energy‐ and temperature‐dependent manner. Here, we further confirm that LMP1 increases the serine phosphorylation level of annexin A2 by activating the phosphoinositide‐specific phospholipase C (PI‐PLC)–PKC α/PKC β pathway, mainly through the activation of the PKCβ pathway. Additionally, active recombinant PKC α, PKC β I, and PKC β II kinases are able to phosphorylate annexin A2 in vitro. Annexin A2 in the nucleus plays an important role in DNA synthesis and cell proliferation. By site‐specific substitution of glutamic acid in the place of serine 11 and 25 in the N‐terminus, we show that serine 25 phosphorylation of annexin A2 was associated with the nuclear entry of annexin A2, DNA synthesis and cell proliferation, whereas serine 11 has no obvious influence. We demonstrate for the first time that the PI‐PLC–PKCα/PKCβ pathway plays an important role in serine phosphorylation and in the nuclear entry of annexin A2 mediated by LMP1. In addition, we show that annexin A2 is the substrate protein of PKC α, PKC βI, and PKC βII kinases. Serine 25 phosphorylation of annexin A2 is shown to be associated with its nuclear entry, DNA synthesis, and cell proliferation.
The International Journal of Biochemistry & Cell Biology | 2012
Zijian Li; Xue Chen; Lili Li; Sufang Liu; Lifang Yang; Xiaoqian Ma; Min Tang; Ann M. Bode; Zigang Dong; Lunquan Sun; Ya Cao
miRNAs (microRNAs) are a class of non-coding small RNAs. The Epstein-Barr-virus (EBV) encoded miR-BHRF1-1 is barely expressed in most nasopharyngeal carcinoma (NPC) cells with EBV latent infection. Here, we used a strategy of overexpression and inhibition of miR-BHRF1-1 and showed that miR-BHRF1-1 is involved in TPA-induced accumulation of EBV lytic proteins and viral copies in late lytic cycle. The data further suggested that the miR-BHRF1-1-potentiated induction of EBV lytic replication was accompanied by inhibiting p53 expression. Our results demonstrated that the EBV original pathogen miR-BHRF1-1 is involved in the control of EBV late lytic replication by directly targeting the host p53 gene.
International Journal of Biological Sciences | 2016
Hongde Li; Sufang Liu; Jianmin Hu; Xiangjian Luo; Namei Li; Ann M. Bode; Ya Cao
Epstein-Barr virus (EBV) has been associated with several types of human cancers. In the host, EBV can establish two alternative modes of life cycle, known as latent or lytic and the switch from latency to the lytic cycle is known as EBV reactivation. Although EBV in cancer cells is found mostly in latency, a small number of lytically-infected cells promote carcinogenesis through the release of growth factors and oncogenic cytokines. This review focuses on the mechanisms by which EBV reactivation is controlled by cellular and viral factors, and discusses how EBV lytic infection contributes to human malignancies.
Cancer Science | 2012
Xuechi Lin; Min Tang; Yongguang Tao; Lili Li; Sufang Liu; Lili Guo; Zijian Li; Xiaoqian Ma; Juan Xu; Ya Cao
The MAPKs are activated by a variety of cellular stimuli to participate in a series of signaling cascades and mediate diverse intracellular responses. One potential target of the MAPKs is Op18/stathmin, a molecule that acts as an integrator of diverse cell signaling pathways and regulates the dynamics of microtubules, which are involved in modulating a variety of cellular processes, including cell cycle progression and cell growth. Our study focused on the regulation of the MAPK‐mediated Op18/stathmin signaling pathway, which is triggered by the Epstein–Barr virus‐encoded latent membrane protein 1 ( LMP1 ) oncogene in nasopharyngeal carcinoma cells. The results showed that the activity of MAPK, which was induced by LMP1, varied with cell cycle progression; LMP1 upregulated phosphorylation of ERK during the G1/S phase, but negatively regulated phosphorylation of ERK during the G2/M phase. We found that the regulation of Op18/stathmin signaling by LMP1 was mainly mediated through ERK. The inhibition of LMP1 expression attenuated the interaction of ERK with Op18/stathmin and promoted microtubule depolymerization. These findings indicate the existence of a new cell cycle‐associated signaling pathway in which LMP1 regulates ERK‐mediated Op18/stathmin signaling. (Cancer Sci 2012; 103: 993–999)
European Journal of Pharmacology | 2008
Sufang Liu; Hai Wang; Zijian Li; Xiyun Deng; Hui Xiang; Yongguang Tao; Wei Li; Min Tang; Ya Cao
Epstein-Barr virus (EBV) infection in tumor cells is generally restricted to the latent forms of viral infection. Switching the latent form of viral infection into the lytic form may induce tumor cell death. High levels of nuclear factor (NF)-kappaB can inhibit EBV lytic replication, and aspirin has the ability to inhibit NF-kappaB activity. The aims of the current study were to determine the effects of aspirin on inducing EBV lytic infection, and thus to reveal the possibility of targeting EBV-positive cancer cells by aspirin. Our results showed that aspirin depleted NF-kappaB (p65) in the nucleus and reactivated EBV into lytic replication. Cells exhibited decreased viability in a dose- and time-dependent manner when incubated with aspirin. When ganciclovir was used in combination with aspirin to treat EBV-positive B95.8 cells and Raji cells, the cytotoxic effect of aspirin was amplified. We demonstrated that aspirin reduced the viability of EBV-positive B lymphocytes due to its ability to induce EBV lytic replication.
Cell Biology International | 2008
Sufang Liu; Hai Wang; Xu-Chi Lin; Hui Xiang; Xiyun Deng; Wei Li; Min Tang; Ya Cao
Epstein—Barr virus (EBV) infection in tumor cells is generally restricted to the latent forms of viral infection. Switching the latent form of viral infection into the lytic form may induce tumor cell death. An important nuclear factor, nuclear factor (NF)‐κB, is thought to play an essential role in EBV lytic infection; high levels of NF‐κB can inhibit EBV lytic replication. In this study, we tested the effect of inducing EBV lytic replication using two NF‐κB inhibitors: Bay11‐7082 and Z‐LLF‐CHO, to reveal the possibility of targeting EBV‐positive cancer therapy with these two NF‐κB inhibitors. Our results showed that Bay11‐7082 and Z‐LLF‐CHO reactivated EBV in a dose‐dependent manner, thus resulting in EBV‐positive 5‐8F cell death. In contrast, there was no significant effect on EBV‐negative HNE3 cells. When ganciclovir was used in combination with either Bay11‐7082 or Z‐LLF‐CHO to treat 5‐8F cells, the cytotoxic effect of the NF‐κB inhibitor was amplified. The finding indicates that inhibiting the NF‐κB activity of EBV‐positive cells can induce lytic replication of EBV and cause lytic cytotoxicity against these cells.
Oncology Reports | 2015
Xiangjian Luo; Xinfang Yu; Sufang Liu; Qipan Deng; Xiaolan Liu; Songling Peng; Hongde Li; Ji-Kai Liu; Ya Cao
The WHO clearly identifies tumors as a curable or a chronic disease. The use of natural agents in cancer prevention and therapy is currently playing an important role. Our laboratory has been investigating various natural phenolic compounds, including grifolin, neoalbaconol and epigallocatechin-3-gallate (EGCG). In the present review, we focus on the anticancer activities and the molecular mechanisms of these compounds. Grifolin, a secondary metabolite isolated from the mushroom Albatrellus confluens, has been shown to inhibit cell growth and induce cell cycle arrest in multiple cancer cell lines by targeting extracellular signal-regulated kinase 1 or by upregulating death-associated protein kinase 1 (DAPK1) via p53. We also demonstrated that neoalbaconol, a novel small-molecular compound with a drimane-type sesquiterpenoid structure obtained from Albatrellus confluens, regulates cell metabolism by targeting 3-phosphoinositide-dependent protein kinase 1 (PDK1) and inhibits cancer cell growth. EGCG, a well known catechin found in tea, has gained much attention for its anticancer effects. Previously, we found that it regulates EBV lytic infection through the phosphoinositide-3 kinase/Akt (PI3K/Akt) and mitogen-activated protein kinase (MAPK) pathways in EBV-positive cancer cells. Therefore, these natural agents could be used as potential leading compounds in the prevention of tumor progression and/or EBV-related cancer.