AXIN-1 protein expression and localization in glioblastoma

Scientific paper - Original scientific paper

• Title (croatian): Izraženost i smještaj proteina aksina u glioblastomima
• Author: Nives Pećina-Šlaus
• Author: Tamara Nikuševa Martić
• Author: Tomislav Kokotović
• Author: Vesna Kušec
• Author: Davor Tomas
• Author: Reno Hrašćan
• Author's institution: University of Zagreb; School of Medicine
• Scientific / art field, discipline and subdiscipline: BIOMEDICINE AND HEALTHCARE; Basic Medical Sciences

Abstract (english)

The etiology and pathogenesis of tumors of the central nervous system are still inadequately explained. In the present study the expression patterns of a critical molecular component of wnt signaling pathway – axin 1 was investigated in 42 patients with glioblastoma, the most aggressive form of glial tumors. Immunostaining and image analysis revealed the quantity and localization of the protein. Downregulation of this tumor suppressor expression was observed in 31% of tumors when compared to the levels of axin in healthy brain tissues. Axin was observed in the cytoplasm in 69% of glioblastoma samples, in 21.4% in both the cytoplasm and nucleus and 9.5% had expression solely in the nucleus. Mean values of relative axin’s expression obtained by image analysis showed that the highest relative quantity of axin was measured when the protein was in the nucleus and the lowest relative quantity of axin when the protein was localized in the cytoplasm. Investigation on axin’s existence at the subcellular level in glioblastomas suggests that axin’s expression and spatial regulation is a dynamic process. Despite increasing knowledge on glioma biology and genetics, the prognostic tools for glioblastoma still need improvement. Our findings on expression of axin 1 may contribute to better understanding of glioblastoma molecular profile.

Abstract (croatian)

Etiologija i patogeneza tumora središnjeg živčanog sustava još uvijek je nedovoljno razjašnjena. U ovoj studiji istraživani su obrasci ekspresije proteina aksina, izuzetno važne molekularne komponente signalnog puta Wnt, u 42 uzorka glioblastoma čovjeka. Imunohistokemijskom metodom i image analizom utvrđena je jačina ekspresije i lokalizacija proteina u stanicama. Smanjena ekspresija ovog tumor supresorskog proteina uočena je u 31% analiziranih tumora usporedbom s razinom ekspresije aksina u normalnom tkivu mozga. U 69% glioblastoma aksin je pronađen u citoplazmi, u 21,4% u jezgri i citoplazmi, dok je u 9,5% glioblastoma lokalizacija bila isključivo u jezgrama. Srednje vrijednosti relativne ekspresije proteina aksina dobivene image analizom pokazuju da je najveća relativna količina aksina izmjerena kada je protein lokaliziran u jezgri, a najmanja relativna količina aksina kada je lokaliziran u citoplazmi. Rezultati istraživanja aksina u glioblastomima na unutarstaničnoj razini pokazuju da je izraženost aksina i njegova prostorna regulacija vrlo dinamičan proces. Unatoč produbljivanju spoznaja o biologiji i genetici glijalnih tumora, saznanja o prognostičkim parametrima za glioblastom još uvijek nisu dostatna. Naši rezultati o razini izraženosti proteina aksina zasigurno će doprinijeti boljem razumijevanju molekularnog profila glioblastoma, te ponuditi potencijalne prognostičke značajke.

• Keywords (english): Adaptor Proteins, Signal Transducing / biosynthesis; Adaptor Proteins, Signal Transducing / metabolism; Adult; Aged; Aged, 80 and over; Axin Protein; Brain Chemistry; Cell Nucleus / metabolism; Cytoplasm / metabolism; Female; Glioblastoma / metabolism; Humans; Immunohistochemistry; Male; Middle Aged; Repressor Proteins / biosynthesis; Repressor Proteins / metabolism
• Language: english
• Publication type: Scientific paper - Original scientific paper
• Publication status: Published
• Peer review: Peer review
• Publication version: Published version
• Journal title: Collegium Antropologicum
• Numbering: vol. 35, no. S. 1, pp. 101-106
• p-ISSN: 0350-6134
• URN:NBN: urn:nbn:hr:105:938585
• Publication: 2011-01
• Document URL: https://hrcak.srce.hr/64050
• Type of resource: Text
• Access conditions: Open access
• Created on: 2024-03-28 12:02:01