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Shiva S. Forootan

Researcher at University of Liverpool

Publications -  26
Citations -  920

Shiva S. Forootan is an academic researcher from University of Liverpool. The author has contributed to research in topics: Prostate cancer & Cancer. The author has an hindex of 15, co-authored 25 publications receiving 788 citations.

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Prognostic significance of osteopontin expression in human prostate cancer

TL;DR: The hypothesis that expression of osteopontin (OPN), an integrin‐binding glycoprotein, can independently predict the potential aggressiveness of prostate cancer is supported and the increased OPN level may be involved in the malignant transformation of prostate epithelial cells and OPN expression level is an important determinant for patient survival is suggested.
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Ribosomal protein L19 is a prognostic marker for human prostate cancer

TL;DR: Investigation of gene expression profiles between benign and malignant human prostate cell lines identified the gene encoding ribosomal protein L19 (RPL19) to be overexpressed in the malignant cells, revealing RPL19 to be a sensitive predictor of prostate cancer progression.
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Increased expression of anterior gradient-2 is significantly associated with poor survival of prostate cancer patients

TL;DR: The results suggest that increased AGR2 expression is a valuable prognostic factor to predict the clinical outcome of the prostate cancer patients.
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Expression of cutaneous fatty acid-binding protein (C-FABP) in prostate cancer: potential prognostic marker and target for tumourigenicity-suppression.

TL;DR: The results suggest that C-FABP may be used as a potential prognostic marker to predict patient outcome and the increased C-fABP expression is a possible target to inhibit the malignant progression of prostate cancer cells.
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Fatty acid activated PPARγ promotes tumorigenicity of prostate cancer cells by up regulating VEGF via PPAR responsive elements of the promoter.

TL;DR: The results suggested that the FABP5-PPARγ-VEGF signal transduction axis, rather than androgen modulated route, may be a more important novel therapeutic target for angiogenesis-suppression treatment of castration resistant prostate cancer.