Aim: The aim of this study was to investigate heat shock protein 90 (HSP90) and topoisomerase I (Topo I) expression and the association between both proteins and clinicopathological parameters of colorectal cancer (CRC), in order to describe their role in tumor biology regarding to Kirsten Ras (KRAS) - positive/negative cases.

Materials And Methods: Expression of HSP90 and Topo I, and KRAS gene mutations were estimated in primary CRCs.

Results: HSP90/Topo I immunophenotype correlated with gender, Duke staging, tumor grade and lymph node metastasis (p<0.01). Positive correlation was found between KRAS mutation and HSP90 expression (p=0.02). HSP90, Topo I expression, and co-expression of HSP90/Topo I correlated with unfavorable parameters of CRCs in respect to KRAS gene status (p<0.001).

Conclusion: Our results revealed that cooperation between HSP90 and Topo I expression exists in CRCs, independently of KRAS gene status, suggesting that co-expression of both proteins might be considered as a double target on individual tumor cells.

Download full-text PDF

Source
http://dx.doi.org/10.21873/anticanres.11905DOI Listing

Publication Analysis

Top Keywords

association hsp90/topoisomerase
4
hsp90/topoisomerase immunophenotype
4
immunophenotype clinical
4
clinical features
4
features colorectal
4
colorectal cancers
4
cancers respect
4
respect gene
4
gene status
4
status aim
4

Similar Publications

Aim: The aim of this study was to investigate heat shock protein 90 (HSP90) and topoisomerase I (Topo I) expression and the association between both proteins and clinicopathological parameters of colorectal cancer (CRC), in order to describe their role in tumor biology regarding to Kirsten Ras (KRAS) - positive/negative cases.

Materials And Methods: Expression of HSP90 and Topo I, and KRAS gene mutations were estimated in primary CRCs.

Results: HSP90/Topo I immunophenotype correlated with gender, Duke staging, tumor grade and lymph node metastasis (p<0.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!