scholarly journals Induction of Tumor Cell Apoptosis or Necrosis by Conditional Expression of Cell Death Proteins: Analysis of Cell Death Pathways and In Vitro Immune Stimulatory Potential

2009 ◽  
Vol 182 (8) ◽  
pp. 4538-4546 ◽  
Author(s):  
Christine Lohmann ◽  
Andreas Muschaweckh ◽  
Susanne Kirschnek ◽  
Luise Jennen ◽  
Hermann Wagner ◽  
...  
Keyword(s):  
Cell Death ◽  
Tumor Cell ◽  
Cell Apoptosis ◽  
Tumor Cell Apoptosis ◽  
Cell Death Pathways ◽  
Conditional Expression

IN VITRO MODULATION OF CISPLATIN-INDUCED TUMOR CELL APOPTOSIS BY INTEGRINS

1996 ◽  
Vol 88 (1-2) ◽  
pp. 77-77
Author(s):  
Fabienne REY ◽  
Martine BOUVIER ◽  
Véronique CAUSSANEL ◽  
Eric TABONE
Keyword(s):  
Tumor Cell ◽  
Cell Apoptosis ◽  
Tumor Cell Apoptosis

scholarly journals Lymphotoxin β receptor mediates caspase-dependent tumor cell apoptosis in vitro and tumor suppression in vivo despite induction of NF-κB activation

2013 ◽  
Vol 34 (5) ◽  
pp. 1105-1114 ◽  
Author(s):  
Xiaolin Hu ◽  
Mary A. Zimmerman ◽  
Kankana Bardhan ◽  
Dafeng Yang ◽  
Jennifer L. Waller ◽  
...  
Keyword(s):  
Tumor Cell ◽  
Cell Apoptosis ◽  
Tumor Suppression ◽  
Tumor Cell Apoptosis ◽  
Β Receptor

Endothelial Cell Protein C Receptor Promotes Apoptosis in Malignant Pleural Mesothelioma Cells

Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 2241-2241
Author(s):  
Shiva Keshava ◽  
L. Vijaya Mohan Rao ◽  
Usha R. Pendurthi
Keyword(s):  
Cell Death ◽  
Tumor Cell ◽  
Cell Apoptosis ◽  
Protein C ◽  
Cytotoxic Effect ◽  
Cell Protein ◽  
Pleural Mesothelioma ◽  
Tumor Cell Apoptosis ◽  
Apoptotic Pathways

Abstract Our recent studies showed that endothelial cell protein C receptor (EPCR) functions as a crucial negative regulator of cancer progression in malignant pleural mesothelioma (MPM) (Keshava et al., Cancer Research 73: 3963-73, 2013). In these studies, the introduction of EPCR expression to aggressive MPM cells lacking EPCR completely attenuated their tumorigenicity whereas the knock-down of EPCR expression in non-aggressive MPM cells that constitutively express EPCR increased their tumorigenicity. This study also revealed that EPCR in MPM cells promotes tumor cell apoptosis in vivo. These data are quite intriguing as EPCR-mediated cell signaling typically activates cell survival and anti-apoptotic pathways and is shown to promote tumor growth in breast and lung cancers. The aim of the present study is to understand the mechanism(s) by which EPCR promotes tumor cell apoptosis in MPM. Evaluation of thoracic fluids obtained from nude mice implanted with MPM cells orthotopically showed a significant increase in the levels of mTNFα and mIFNγ in mice implanted with REN (+EPCR) cells compared to mice implanted with parental REN MPM or REN cells transfected with the vector control [REN(z)]. Analysis of tumor cell apoptosis of cultured cells by TUNEL assay showed that REN (+EPCR) cells were highly susceptible to TNFα+IFNγ-induced cell death compared to parental REN or REN(z) cells (80% vs. 20% cell death at 72 h). In agreement with the concept that EPCR in MPM cells promotes the apoptosis, M9K MPM cells that constitutively express EPCR (non-aggressive MPM cell line) were highly susceptible to TNFα+IFNγ-induced cell death; the knock-down of EPCR in these cells rendered them resistant to cytokine-induced cell death. EPCR-induced tumor cell apoptosis in MPM cells was not dependent on activated protein C (APC). Deletion of the cytoplasmic tail of EPCR failed to diminish its cytotoxic effect. Analysis of REN and REN(+EPCR) tumor cell extracts using PathScan intracellular signaling antibody array kit (Cell Signaling Technology, MA) and immunoblot analysis with specific antibodies against proteins involved in apoptotic pathways revealed that EPCR expression in MPM cells, in comparison to MPM cells lacking EPCR, resulted in a sustained cleavage of poly ADP ribose polymerase (PARP) and an enhanced activation of caspase 3 in response to TNFα+ IFNγ treatment. In addition, REN(+EPCR) cells exhibited an increased activation of caspase 8 and a decreased phosphorylation of anti-apoptotic protein BAD. Further signaling studies showed a delayed activation of NF-kB, suppression of activation of STAT3 and AKT in REN(+EPCR) cells compared to REN cells in response to TNFα+ IFNγ treatment. In addition, EPCR expression suppressed the constitutive activation of the proline-rich AKT substrate, 40 kDa (PRAS40). Overall, our studies indicate that EPCR in MPM cells controls the progression of MPM by exerting its effect at multiple levels. First, EPCR in MPM cells elicits elaboration of cytokines TNFα and IFNγ in vivo and then renders the MPM cells susceptible to TNFα+ IFNγ-induced cell death. The EPCR-mediated cytotoxic effect in MPM cells is independent of APC and the cytoplasmic tail and involves the suppression of STAT3 and AKT activation. At present, it is unclear exactly how EPCR initiates the activation of the apoptotic pathway in MPM cells and whether it involves the interaction of EPCR with the endogenous ligand(s) specific to MPM cells. Studies are underway to identify EPCR interacting proteins in MPM cells. Disclosures No relevant conflicts of interest to declare.

scholarly journals Dual-colour (near-infrared/visible) emitting annexin V for fluorescence imaging of tumour cell apoptosis in vitro and in vivo

RSC Advances ◽  
2020 ◽  
Vol 10 (63) ◽  
pp. 38244-38250
Author(s):  
Setsuko Tsuboi ◽  
Takashi Jin
Keyword(s):  
Tumor Cell ◽  
Indocyanine Green ◽  
Fluorescence Imaging ◽  
Cell Apoptosis ◽  
Near Infrared ◽  
Annexin V ◽  
Tumor Cell Apoptosis ◽  
Dual Colour

Indocyanine green labeled recombinant annexin V probes (ICG–EGFP–Annexin V and ICG–mPlum–Annexin V) were synthesized for near-infrared and visible fluorescence imaging of tumor cell apoptosis both in vitro and in vivo.

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