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王树林, Mijin Kim, Jessica Liao, Melissa L. Dowling, K. Ranh Voong, Sharon E. Parker, Shulin Wang, Wafik S. El-Deiry, and Gary D. Kao
Cancer Res 2008; 68 (9). May1, 2008, 3440-3449,-0001,():
-1年11月30日
Tumor necrosis factor–related apoptosis–inducing ligand (TRAIL) has attracted interest as an anticancer treatment, when used in conjunction with standard chemotherapy. We investigated the mechanistic basis for combining low-dose TRAIL with microtubule-targeting agents that invoke the mitotic checkpoint. Treatment of T98G and HCT116 cells with nocodazole alone resulted in a robust mitotic block with initially little cell death; low levels of cell death were also seen with TRAIL alone at 10ng/mL final concentration. In contrast, the addition of low-dose TRAIL to nocodazole was associated with maximally increased caspase-3, caspase-8, and caspase-9 activation, which efficiently abrogated the mitotic delay and markedly increased cell death. In contrast, the abrogation of mitotic checkpoint and increased cell death were blocked by inhibitors of caspase-8 and caspase-9 or pan-caspase inhibitor. The addition of TRAIL to either nocodazole or paclitaxel (Taxol) reduced levels of the mitotic checkpoint proteins BubR1 and Bub1. BubR1 mutated for the caspase cleavage sites, but not wild-type BubR1, was resistant to cleavage induced by TRAIL added to nocodazole, and partially blocked the checkpoint abrogation. These resultssuggest that adding a relatively low concentration of TRAIL to antimicrotubule agents markedly increases complete caspase activation. This in turn accentuates degradation of spindle checkpoint proteins such as BubR1 and Bub1, contributes to abrogation of the mitotic checkpoint, and induces cancer cell death. These results suggest that TRAIL may increase the anticancer efficacy of microtubule-targeting drugs. [Cancer Res 2008;68 (9):3440–9]
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【期刊论文】TRAIL and apoptosis induction by TNF-family death receptors
王树林, Shulin Wang and Wafik S El-Deiry*,
Oncogene 22 (2003) 8628-8633 ,-0001,():
-1年11月30日
Tumor necrosis factor-related apoptosis-inducing ligand or Apo 2 ligand (TRAIL/Apo2L) is a member of the tumor necrosis factor (TNF) family of ligands capable of initiating apoptosis through engagement of its death receptors. TRAIL selectively induces apoptosis of a variety of tumor cells and transformed cells, but not most normal cells, and therefore has garnered intense interest as a promising agent for cancer therapy. TRA IL is expressed on different cells of the immune system and plays a role in both T-cell-and natural killer cell-mediated tumor surveillance and suppression of suppressing tumor metastasis. Som e mismatch-repair-deficient tumors evade TRAIL-induced apoptosis and acquire TRAIL resistance through different mechanisms. Deat hreceptors, members of the TNF receptor family, signal apoptosis independently of the p53 tumor-suppressor gene. TRAIL treatment in combination with chemo-or radiotherapy enhances TRAIL sensitivity or reverses TRAIL resistance by regulating the downstream effectors. Efforts to identify agents that activate death receptors or block specific effectors may improve therapeutic design. In this review, we summarize recent insights into the apoptosis-signaling pathways stimulated by TRAIL, present our current understanding of the physiological role of this ligand and the potential of its application for cancer therapy and prevention.
tumor necrosis factor (, TNF), -related apoptosis-inducing ligand (, TRAIL), , tumor necrosis factor receptor family, p53, apoptosis, cancer therapy
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【期刊论文】TpMRK regulates cell division of Tetrahymena in response to oxidative stress
王树林, Wenzhou Li y, Siwei Zhang y, Osamu Numata, Yoshinori Nozawa, and Shulin Wang*, y
Oncogene (2008) 27, 6207-6215,-0001,():
-1年11月30日
TpMRK was identified as a stress-responsive mitogen activated protein kinase (MAPK)-related kinase and has been shown to play a critical role in the stress signalling in Tetrahymena cells. Here, we found that the mRNA expression of TpMRK was correlated with cell division of Tetrahymena with decreased expression occurring in cells prior to entering synchronous cell division induced by heat treatment. Notably, cell division was delayed with a lower division index of 40% after exposure to hydrogen peroxide while 85% of cells underwent cell division synchronously at 75 min after heat treatment without the oxidative exposure. Furthermore, inactivation of TpMRK signalling by p38 MAPK inhibitor SB203580 or MEK inhibitor PD 98059 partially derepressed cell division induced by hydrogen peroxide. Our data suggest that oxidative stimuli might cause aberration of synchronous cell division of Tetrahymena through activating the TpMRK cascade. Copyright # 2009 John Wiley & Sons, Ltd.
cell division, mitogen-activated protein kinase, oxidative stress, protozoan, reactive oxygen species, TpMRK
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王树林, S Wang
Oncogene (2008) 27, 6207-6215 & 2008 Macmillan Publishers Limited All rights reserved 0950-9232/08 $32.00,-0001,():
-1年11月30日
Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL)is a member of the TNF superfamily and has been shown to induce apoptosis in cancer cells but not normal cells. TRAIL triggers apoptosis through binding to its receptors DR4 and KILLER/DR5. Chemo or radiotherapy induces apoptosis through activation of p53 in response to cellular damage, whereas TRAIL induces apoptosis independent of p53. Mutations or deletions of p53 occurred in more than half of human tumors confer resistance to chemo-radiotherapy. Treatment of TRAILresistant tumors with agents targeting death receptors, intrinsic Bcl-2 family members, inhibitor of apoptosis proteins or PI3K/Akt pathway restores the sensitivity to TRAIL-induced apoptosis. Combination of rhTRAIL or the agonist antibody for TRAIL receptor with conventional chemotherapeutic agents results in enhanced efficacy in preventing tumor progression and metastasis. Therefore, the rational design of TRAIL-based therapy combining with other modality that either synergizes to apoptosis induction or overcomes the resistance represents a challenging strategy to achieve the systemic tumor targeting and augment the antitumor activity of cancer therapeutics.
tumor necrosis factor-related apoptosisinducing ligand, TNF receptor superfamily, DR4, KILLER/, DR5, apoptosis, cancer therapy
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王树林, Bradley A. Carlson‡, Mohamed E. Moustafa‡, , Aniruddha Sengupta‡, Ulrich Schweizer§, Rajeev Shrimali‡, Mahadev Rao‡, Nianxin Zhong‡, Shulin Wang‡, Lionel Feigenbaum¶, Byeong Jae Lee, Vadim N. Gladyshev**, and Dolph L. Hatfield‡
THE JOURNAL OF BIOLOGICAL CHEMISTRY VOL.282 NO.45 (2007) 32591-32602 ,-0001,():
-1年11月30日
From the ‡ Molecular Biology of Selenium Section, Laboratory of Cancer Prevention, Center for Cancer Research, NCI, National Institutes of Health, Bethesda, Maryland 20892, §Neurobiology of Selenium, Neuroscience Research Center, Institute forExperimental Endocrinology, Charite Universita tsmedizin Berlin, 10117 Berlin, Germany, ¶ Science Applications International Corporation, Frederick Cancer Research and Development Center, Frederick, Maryland 21702, the School of Biological Sciences and Institute of Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Korea, and the **Department of Biochemistry, University of Nebraska, Lincoln, Nebraska 68588
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