Epigenetic control of defense genes following MeJA-induced priming in rice (O. sativa).

In plant defense, priming is a physiological process by which a plant prepares to more quickly or aggressively respond to a future biotic or abiotic stress. This unique physiological state can be induced by beneficial microbes or by treatment with natural or synthetic compounds. Priming has been described copiously, mainly in dicots, but the study on the molecular mechanisms regulating the phenomenon is still at its infancy. A fascinating possibility is that epigenetic changes may be the main actors on priming establishment. A more accessible chromatin structure, due to DNA methylation and/or histone modifications, could facilitate a quicker and more potent gene response to a subsequent attack. Here, we investigated the impact of methyl jasmonate (MeJA)-induced priming on the response efficacy to mechanical wounding of a monocot (Oryza sativa). In particular, we showed that MeJA primes plants for increased expression of defense-related genes, such as OsBBPI and OsPOX, upon wounding. Finally, we provided evidence that MeJA modulates histone modifications in the promoter region of OsBBPI, as well as changes at genome-wide DNA methylation level. Together these studies corroborate the importance of priming in strengthening plant defense and support the growing evidence that epigenetic regulation plays a pivotal role in priming onset.

Two-dimensional neovascular complexity is significantly higher in nontumor prostate tissue than in low-risk prostate cancer

PURPOSE: Prostate cancer is the most frequent cancer in men in Europe. A major focus in urology is the identification of new biomarkers with improved accuracy in patients with low-risk prostate cancer. Here, we evaluated two-dimensional neovascular complexity in prostate tumor and nontumor biopsy cores by use of a computer-aided image analysis system and assessed the correlations between the results and selected clinical and pathological parameters of prostate carcinoma. MATERIALS AND METHODS: A total of 280 prostate biopsy sections from a homogeneous series of 70 patients with low-risk prostate cancer (Gleason score 3+3, prostate-specific antigen [PSA]<10 ng/mL, and clinical stage T1c) who underwent systematic biopsy sampling and subsequent radical prostatectomy were analyzed. For each biopsy, 2-microm sections were treated with CD34 antibodies and were digitized by using an image analysis system that automatically estimates the surface fractal dimension. RESULTS: Our results showed that biopsy sections without cancer were significantly more vascularized than were tumors. No correlations were found between the vascular surface fractal dimension and patient's age, PSA and free-to-total PSA ratios, pathological stage, Gleason score, tumor volume, vascular invasion, capsular penetration, surgical margins, and biochemical recurrence. CONCLUSIONS: The value of angiogenesis in prostate cancer is still controversial. Our findings suggest that low-risk prostate cancer tissues are less vascularized than are nontumor tissues. Further studies are necessary to understand whether angiogenesis is a hallmark of intermediate- and high-risk prostate cancer.