Literature DB >> 16292484

Immunocytochemical detection of 14-3-3 in primary nervous system tumors.

Wei-Dong Cao1, Xiang Zhang, Jian-Ning Zhang, Zhi-Jun Yang, Hai-Ning Zhen, Guang Cheng, Bian Li, Dakuan Gao.   

Abstract

14-3-3 proteins have attracted much recent interest in the etiopathogenesis of human cancers owing to their involvement in the prevention of apoptosis. However, the expression of 14-3-3 in primary nervous system tumors has not been previously characterized. In this paper, Immunohistochemistry using a specific anti-14-3-3 antibody was performed on formalin-fixed, paraffin embedded archival tissue from 124 primary human nervous system tumors and 10 normal brain tissues. In the normal control brains, 14-3-3 immunoreactivity was localized mainly in the neuronal somata and processes, and some glial cells showed only weak immunoreactivity. However, 14-3-3 immunoreactivity was seen in the majority of astrocytomas [grade I (9/11), II (16/21), III (13/17), IV (17/21)]. There was no difference between the positive expression rates of 14-3-3 in different grades of astrocytomas (P = 0.968). But the intensity and degree of 14-3-3 immunoreactivity in diffuse astrocytomas, anaplastic astrocytoma, and glioblastoma multiformes showed trends with tumor grade, with glioblastomas having the highest positivity (P = 0.048). The 14-3-3 immunoreactivity was also seen in the majority of other gliomas [oligodendroglioma (2/3), anaplastic oligodendroglioma (4/4), ependymoma (1/2), anaplastic ependymoma (2/2), choroid plexus papilloma (3/3), pineocytoma (2/2), medulloblastoma (5/8)]. All meningiomas [syncytical (3), fibrous/fibroblastic (4), angiomatous (4), transitional/mixed (3)] were intensely and diffusely positive. All schwannomas (4), neurofibromas (2), pituitary adenomas (6) and craniopharyngiomas(4) also showed intense positive staining. These results showed that 14-3-3 is expressed in the majority of the primary human nervous system tumors. The up-regulated expression of 14-3-3 may be a common mechanism for evading apoptosis in most primary human nervous system tumors, and targeting 14-3-3 may be a novel promising strategy for the treatment of these tumors, especially for malignant tumors.

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Year:  2005        PMID: 16292484     DOI: 10.1007/s11060-005-9027-7

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  31 in total

1.  Functional conservation of 14-3-3 isoforms in inhibiting bad-induced apoptosis.

Authors:  R R Subramanian; S C Masters; H Zhang; H Fu
Journal:  Exp Cell Res       Date:  2001-11-15       Impact factor: 3.905

2.  Serine phosphorylation of death agonist BAD in response to survival factor results in binding to 14-3-3 not BCL-X(L)

Authors:  J Zha; H Harada; E Yang; J Jockel; S J Korsmeyer
Journal:  Cell       Date:  1996-11-15       Impact factor: 41.582

3.  Antibodies against the major brain isoforms of 14-3-3 protein. An antibody specific for the N-acetylated amino-terminus of a protein.

Authors:  H Martin; Y Patel; D Jones; S Howell; K Robinson; A Aitken
Journal:  FEBS Lett       Date:  1993-10-04       Impact factor: 4.124

4.  Evidence for phosphatidylinositol 3-kinase-Akt-p7S6K pathway activation and transduction of mitogenic signals by platelet-derived growth factor in meningioma cells.

Authors:  Mahlon D Johnson; Evelyn Okedli; Ann Woodard; Steven A Toms; George S Allen
Journal:  J Neurosurg       Date:  2002-09       Impact factor: 5.115

5.  Apoptosis in nontumorous and neoplastic human pituitaries: expression of the Bcl-2 family of proteins.

Authors:  E Kulig; L Jin; X Qian; E Horvath; K Kovacs; L Stefaneanu; B W Scheithauer; R V Lloyd
Journal:  Am J Pathol       Date:  1999-03       Impact factor: 4.307

6.  Suppression of apoptosis signal-regulating kinase 1-induced cell death by 14-3-3 proteins.

Authors:  L Zhang; J Chen; H Fu
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-20       Impact factor: 11.205

7.  Expression pattern of apoptotic markers in vestibular schwannomas.

Authors:  Christian Mawrin; Elmar Kirches; Knut Dietzmann; Albert Roessner; Carsten Boltze
Journal:  Pathol Res Pract       Date:  2002       Impact factor: 3.250

Review 8.  Molecular neuro-oncology and the development of targeted therapeutic strategies for brain tumors. Part 4: p53 signaling pathway.

Authors:  Herbert B Newton
Journal:  Expert Rev Anticancer Ther       Date:  2005-02       Impact factor: 4.512

9.  Human 14-3-3 protein: radioimmunoassay, tissue distribution, and cerebrospinal fluid levels in patients with neurological disorders.

Authors:  P F Boston; P Jackson; R J Thompson
Journal:  J Neurochem       Date:  1982-05       Impact factor: 5.372

10.  14-3-3-affinity purification of over 200 human phosphoproteins reveals new links to regulation of cellular metabolism, proliferation and trafficking.

Authors:  Mercedes Pozuelo Rubio; Kathryn M Geraghty; Barry H C Wong; Nicola T Wood; David G Campbell; Nick Morrice; Carol Mackintosh
Journal:  Biochem J       Date:  2004-04-15       Impact factor: 3.857

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  7 in total

Review 1.  Choroid plexus papillomas: advances in molecular biology and understanding of tumorigenesis.

Authors:  Michael Safaee; Michael C Oh; Orin Bloch; Matthew Z Sun; Gurvinder Kaur; Kurtis I Auguste; Tarik Tihan; Andrew T Parsa
Journal:  Neuro Oncol       Date:  2012-11-21       Impact factor: 12.300

2.  Trafficking of neuronal two pore domain potassium channels.

Authors:  Alistair Mathie; Kathryn A Rees; Mickael F El Hachmane; Emma L Veale
Journal:  Curr Neuropharmacol       Date:  2010-09       Impact factor: 7.363

3.  Rac1 activation driven by 14-3-3ζ dimerization promotes prostate cancer cell-matrix interactions, motility and transendothelial migration.

Authors:  Anna Goc; Maha Abdalla; Ahmad Al-Azayzih; Payaningal R Somanath
Journal:  PLoS One       Date:  2012-07-13       Impact factor: 3.240

Review 4.  Interaction between Rho GTPases and 14-3-3 Proteins.

Authors:  Daniel Brandwein; Zhixiang Wang
Journal:  Int J Mol Sci       Date:  2017-10-15       Impact factor: 5.923

5.  Rac1 S71 Mediates the Interaction between Rac1 and 14-3-3 Proteins.

Authors:  Abdalla Abdrabou; Daniel Brandwein; Changyu Liu; Zhixiang Wang
Journal:  Cells       Date:  2019-08-30       Impact factor: 6.600

6.  Differential Subcellular Distribution and Translocation of Seven 14-3-3 Isoforms in Response to EGF and During the Cell Cycle.

Authors:  Abdalla Abdrabou; Daniel Brandwein; Zhixiang Wang
Journal:  Int J Mol Sci       Date:  2020-01-02       Impact factor: 5.923

Review 7.  Emerging roles of 14-3-3γ in the brain disorder.

Authors:  Eunsil Cho; Jae-Yong Park
Journal:  BMB Rep       Date:  2020-11       Impact factor: 4.778

  7 in total

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