Literature DB >> 2428168

The cellular tumour antigen p53: evidence for transformation-related, immunological variants of p53.

J Milner, A Cook.   

Abstract

The protein p53 is involved in the control of normal cell proliferation. However, when expressed abnormally, p53 also contributes to the process of cell transformation. The possibility that multifunctional forms of p53 exist was realised when two cell cycle dependent forms of the protein were identified in normal cells (lymphocytes: J. Milner, 1984, Nature (London) 310, 143-145). Interestingly these two forms of p53 in normal cells lack some of the epitopes recognised by monoclonal antibodies developed against p53 in transformed cells. This suggests that p53 may bear additional transformation-related epitopes in transformed cells. We have now investigated this possibility by screening a variety of cell lines for immunological variants of p53. The monoclonal antibodies PAb421, PAb122, RA3.2C2, PAb248, PAb200.47, and PAb246 were used. Our results indicate the existence of two immunologically distinct variants of p53 expressed in transformed cells. The two p53 variants are distinguished by the presence or absence of the epitope recognised by PAb246. A given cell line generally expressed a single immunological variant of p53. However, 3T6 cells expressed two subsets of p53 and appeared to modulate p53 synthesis in response to cell density.

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Year:  1986        PMID: 2428168     DOI: 10.1016/0042-6822(86)90426-5

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  9 in total

1.  Stabilization of the p53 transformation-related protein in mouse fibrosarcoma cell lines: effects of protein sequence and intracellular environment.

Authors:  O Halevy; A Hall; M Oren
Journal:  Mol Cell Biol       Date:  1989-08       Impact factor: 4.272

2.  Tumor suppressor p53: analysis of wild-type and mutant p53 complexes.

Authors:  J Milner; E A Medcalf; A C Cook
Journal:  Mol Cell Biol       Date:  1991-01       Impact factor: 4.272

3.  Mutant p53 tumor suppressor alleles release ras-induced cell cycle growth arrest.

Authors:  G G Hicks; S E Egan; A H Greenberg; M Mowat
Journal:  Mol Cell Biol       Date:  1991-03       Impact factor: 4.272

4.  p53 DNA binding can be modulated by factors that alter the conformational equilibrium.

Authors:  K G McLure; P W Lee
Journal:  EMBO J       Date:  1999-02-01       Impact factor: 11.598

5.  Activating mutations for transformation by p53 produce a gene product that forms an hsc70-p53 complex with an altered half-life.

Authors:  C A Finlay; P W Hinds; T H Tan; D Eliyahu; M Oren; A J Levine
Journal:  Mol Cell Biol       Date:  1988-02       Impact factor: 4.272

6.  Characterization of mutant p53-hsp72/73 protein-protein complexes by transient expression in monkey COS cells.

Authors:  H W Stürzbecher; C Addison; J R Jenkins
Journal:  Mol Cell Biol       Date:  1988-09       Impact factor: 4.272

7.  Evidence for allosteric variants of wild-type p53, a tumour suppressor protein.

Authors:  A Cook; J Milner
Journal:  Br J Cancer       Date:  1990-04       Impact factor: 7.640

Review 8.  Mutant p53 and ETS2, a Tale of Reciprocity.

Authors:  Luis Alfonso Martinez
Journal:  Front Oncol       Date:  2016-02-18       Impact factor: 6.244

9.  High Mobility Group Box 1 Influences HSV1716 Spread and Acts as an Adjuvant to Chemotherapy.

Authors:  Leslee Sprague; Joel M Lee; Brian J Hutzen; Pin-Yi Wang; Chun-Yu Chen; Joe Conner; Lynne Braidwood; Kevin A Cassady; Timothy P Cripe
Journal:  Viruses       Date:  2018-03-15       Impact factor: 5.048

  9 in total

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