Literature DB >> 10799856

Cutting edge: the tumor counterattack hypothesis revisited: colon cancer cells do not induce T cell apoptosis via the Fas (CD95, APO-1) pathway.

N Favre-Felix1, A Fromentin, A Hammann, E Solary, F Martin, B Bonnotte.   

Abstract

The counterattack hypothesis, suggesting that cancer cells express Fas ligand (FasL) and are able to kill Fas-expressing tumor-infiltrating activated T cells, was supported by reports of the killing of Jurkat cells by FasL-expressing human colon cancer cell lines. Through the use of an improved cytotoxic assay in which soluble FasL and FasL-transfected KFL9 cells were used as positive controls, we show that none of seven human colon cancer cell lines induce apoptosis of two Fas-expressing target cell lines, Jurkat and L1210-Fas cells. Moreover, in coculture experiments, cancer cell monolayers do not inhibit the growth of Fas-expressing lymphoid cells. Although FasL mRNA and protein were detected in the extracts of the colon cancer cell lines, flow cytometry and confocal microscopy failed to detect the protein on the surface of tumor cells. These results suggest that the counterattack of tumor-infiltrating T lymphocytes by cancer cells may not account for immune tolerance toward tumor cells.

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Year:  2000        PMID: 10799856     DOI: 10.4049/jimmunol.164.10.5023

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  16 in total

1.  Countering the 'counterattack' hypothesis.

Authors:  N P Restifo
Journal:  Nat Med       Date:  2001-03       Impact factor: 53.440

2.  Soluble FAS in the prediction of benefit from cetuximab and irinotecan for patients with advanced colorectal cancer.

Authors:  Jordi Codony-Servat; Xabier Garcia-Albeniz; Carles Pericay; Vicente Alonso; Pilar Escudero; Carlos Fernández-Martos; Rosa Gallego; Anna Martínez-Cardús; Eva Martinez-Balibrea; Joan Maurel
Journal:  Med Oncol       Date:  2013-01-22       Impact factor: 3.064

Review 3.  Colon cancer and the immune system: the role of tumor invading T cells.

Authors:  Maximilian Waldner; Carl-C Schimanski; Markus-F Neurath
Journal:  World J Gastroenterol       Date:  2006-12-07       Impact factor: 5.742

4.  Impaired CD95 expression predisposes for recurrence in curatively resected colon carcinoma: clinical evidence for immunoselection and CD95L mediated control of minimal residual disease.

Authors:  J Sträter; U Hinz; C Hasel; U Bhanot; G Mechtersheimer; T Lehnert; P Möller
Journal:  Gut       Date:  2005-05       Impact factor: 23.059

5.  The regulation of FasL expression during activation-induced cell death (AICD).

Authors:  T Nguyen; J Russell
Journal:  Immunology       Date:  2001-08       Impact factor: 7.397

Review 6.  CD95 (Fas/APO-1)/CD95L in the gastrointestinal tract: fictions and facts.

Authors:  J Sträter; P Möller
Journal:  Virchows Arch       Date:  2003-02-11       Impact factor: 4.064

7.  Upregulation of tumour associated antigen RCAS1 is implicated in high stages of colorectal cancer.

Authors:  K Leelawat; T Watanabe; M Nakajima; S Tujinda; C Suthipintawong; V Leardkamolkarn
Journal:  J Clin Pathol       Date:  2003-10       Impact factor: 3.411

Review 8.  Immune-epithelial crosstalk at the intestinal surface.

Authors:  Nadine Wittkopf; Markus F Neurath; Christoph Becker
Journal:  J Gastroenterol       Date:  2014-01-28       Impact factor: 7.527

9.  Relevance of target cell-induced apoptosis as mechanism of resistance against natural killer cells.

Authors:  Justin Hasenkamp; Andrea Borgerding; Gerald Wulf; Norbert Schmitz; Lorenz Truemper; Bertram Glass
Journal:  Ann Hematol       Date:  2009-10-13       Impact factor: 3.673

10.  Bile salt-induced apoptosis in human colon cancer cell lines involves the mitochondrial transmembrane potential but not the CD95 (Fas/Apo-1) receptor.

Authors:  Frank-Peter Wachs; René C Krieg; Cecilia M P Rodrigues; Helmut Messmann; Frank Kullmann; Ruth Knüchel-Clarke; Jürgen Schölmerich; Gerhard Rogler; Klaus Schlottmann
Journal:  Int J Colorectal Dis       Date:  2004-09-07       Impact factor: 2.571

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