LABORATORY RESEARCH Cancer Genetics-Guided Discovery of Serum Biomarker Signatures for Diagnosis and Prognosis of Prostate Cancer Scientists describe a two-stage strategy for the discovery of serum biomarker signatures corresponding to specific cancer-causing mutations and its application to prostate cancer in the context of the commonly occurring phosphatase and tensin homolog tumor-suppressor gene inactivation. [Proc Natl Acad Sci USA] Peroxiredoxin 1 Controls Prostate Cancer Growth through Toll-Like Receptor 4-Dependent R egulation of Tumor Vasculature Researchers show that peroxiredoxin 1 is overexpressed in human prostate cancer specimens and that it regulates prostate tumor growth through toll-like receptor 4-dependent regulation of prostate tumor vasculature. [Cancer Res] Systematic Analysis of MicroRNAs Targeting the Androgen Receptor in Prostate Cancer Cells To systematically characterize mechanisms involving microRNAs (miRNAs), investigators conducted a gain-of function screen of 1129 miRNA molecules in a panel of human prostate cancer cell lines and quantified changes in androgen receptor protein content using protein lysate microarrays. [Cancer Res] Prostate Cancer Predisposition Loci and Risk of Metastatic Disease and Prostate Cancer Recurrence Single nucleotide polymorphisms in MSMB and 8q24 which predispose to prostate cancer overall are associated with risk for metastatic prostate cancer. [Clin Cancer Res] Inhibition of Prostate Cancer Osteoblastic Progression with VEGF121/rGel, a Single Agent Targeting Osteoblasts, Osteoclasts, and Tumor Neovasculature Scientists previously reported that VEGF121/rGel targets osteoclast precursors and tumor neovasculature. Here, they tested the hypothesis that targeting non-tumor cells expressing these receptors can inhibit tumor progression in a clinically relevant model of osteoblastic prostate cancer. [Clin Cancer Res] Arachidonic Acid Pathway Members PLA2G7, HPGD, EPHX2, and CYP4F8 Identified as Putative Novel Therapeutic Targets in Prostate Cancer Investigators identified four novel putative therapeutic targets with biomarker potential for different subtypes of prostate cancer. [Am J Pathol] Identification of Clinically Relevant Protein Targets in Prostate Cancer with 2D-DIGE Coupled Mass Spectrometry and Systems Biology Network Platform Researchers compared the individual protein expression patterns from histologically characterized prostate cancer and the surrounding benign tissue obtained by manual micro dissection using highly sensitive two-dimensional differential gel electrophoresis (2D-DIGE) coupled with mass spectrometry. [PLoS One] TRPV6 Determines the Effect of Vitamin D3 on Prostate Cancer Cell Growth Scientists demonstrate that in low steroid conditions 1,25-dihydroxyvitamin D3 upregulates the expression of TRPV6, enhances the proliferation by increasing the number of cells entering into S-phase. [PLoS One] Expression Profile of WNT Molecules in Prostate Cancer and its Regulation by Aminobisphosphonates Since the WNT signaling pathway regulates bone remodeling and has been implicated in tumor progression and osteomimicry, investigators analyzed the WNT profile of primary prostate cancer (PCa) tissues and PCa cell lines and assessed its regulation by bisphosphonates. [J Cell Biochem] CLINICAL RESEARCH An Empirical Evaluation of Guidelines on Prostate-specific Antigen Velocity in Prostate Cancer Detection Scientists found no evidence to support the recommendation that men with high prostate-specific antigen velocity should be biopsied in the absence of other indications; this measure should not be included in practice guidelines. [J Natl Cancer Inst] Association Between Single Nucleotide Polymorphisms in the Gene for XRCC1 and Radiation-Induced Late Toxicity in Prostate Cancer Patients The purpose of the present prospective investigation was to evaluate the association of single nucleotide polymorphisms in X-ray repair cross-complementing group 1 (XRCC1) with radiation-induced late side effects in prostate cancer patients treated with radiotherapy. [Radiother Oncol] |