Literature DB >> 16404353

Patterns of expression of TSC-22 protein in astrocytic gliomas.

K O Shostak1, V V Dmitrenko, M I Vudmaska, V G Naidenov, A V Beletskii, T A Malisheva, V M Semenova, Yu P Zozulya, J Demotes-Mainard, V M Kavsan.   

Abstract

AIM: To evaluate expression patterns of protein product of putative tumor suppressor gene TSC-22 in human astrocytic tumors by immunohistochemical approach.
METHODS: Plasmid pET-23d-TSC22 was constructed for the expression of human TSC-22 protein in bacterial system, and polyclonal rabbit antibodies against recombinant TSC-22 were produced. Immunohistochemical analysis of TSC-22 and GFAP expression with the use of anti-human-TSC-22- and anti-human-GFAP-antibodies was performed on histological slides of astrocytic tumors.
RESULTS: Immunohistochemical analysis has shown that the number of cells expressing TSC-22 was significantly lower in glioblastoma tissues than that in diffuse astrocytoma. Double immunohistochemical staining of astrocytic tumors using anti-human-TSC-2- and anti-human-GFAP-antibodies showed that both TSC-22 and GFAP expression is co-localized in astrocytes.
CONCLUSION: TSC-22 protein is expressed in astrocytes, but not in macrophage/microglial cells. In more aggressive forms of astrocytic tumors decreased expression of TSC-22 mRNA correlates with its lowered expression on protein level.

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Year:  2005        PMID: 16404353

Source DB:  PubMed          Journal:  Exp Oncol        ISSN: 1812-9269


  6 in total

1.  Antagonistic TSC22D1 variants control BRAF(E600)-induced senescence.

Authors:  Cornelia Hömig-Hölzel; Remco van Doorn; Celia Vogel; Markus Germann; Marco G Cecchini; Els Verdegaal; Daniel S Peeper
Journal:  EMBO J       Date:  2011-03-29       Impact factor: 11.598

2.  Madm (Mlf1 adapter molecule) cooperates with Bunched A to promote growth in Drosophila.

Authors:  Silvia Gluderer; Erich Brunner; Markus Germann; Virginija Jovaisaite; Changqing Li; Cyrill A Rentsch; Ernst Hafen; Hugo Stocker
Journal:  J Biol       Date:  2010-02-11

3.  Yeast two-hybrid screening identified WDR77 as a novel interacting partner of TSC22D2.

Authors:  Qiao Li; Pan Chen; Zhaoyang Zeng; Fang Liang; Yali Song; Fang Xiong; Xiayu Li; Zhaojian Gong; Ming Zhou; Bo Xiang; Cong Peng; Xiaoling Li; Xiang Chen; Guiyuan Li; Wei Xiong
Journal:  Tumour Biol       Date:  2016-06-23

4.  The Drosophila homolog of human tumor suppressor TSC-22 promotes cellular growth, proliferation, and survival.

Authors:  Xiaodong Wu; Megumu Yamada-Mabuchi; Erick J Morris; Pradeep Singh Tanwar; Leonard Dobens; Silvia Gluderer; Sabina Khan; Jing Cao; Hugo Stocker; Ernst Hafen; Nick J Dyson; Laurel A Raftery
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-28       Impact factor: 11.205

5.  Crucial role of TSC-22 in preventing the proteasomal degradation of p53 in cervical cancer.

Authors:  Cheol-Hee Yoon; Seung Bae Rho; Seong-Tae Kim; Seongho Kho; Junsoo Park; Ik-Soon Jang; Seonock Woo; Sung Soon Kim; Je-Ho Lee; Seung-Hoon Lee
Journal:  PLoS One       Date:  2012-08-01       Impact factor: 3.240

6.  TSC-22 up-regulates collagen 3a1 gene expression in the rat heart.

Authors:  Annina Kelloniemi; Jani Aro; Juha Näpänkangas; Elina Koivisto; Erja Mustonen; Heikki Ruskoaho; Jaana Rysä
Journal:  BMC Cardiovasc Disord       Date:  2015-10-13       Impact factor: 2.298

  6 in total

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