MORPHOLOGICAL AND BIOMECHANICAL CORRELATION IN THE TENNIS ELBOW

With the definition of 'Tennis Elbow' are rubricated a series of pathologies which recognize a common origin in a damage on a level of the myotendon jointing apparatus. A decodification in biochemical molecular key of the jointing apparatus consents to identify a series of microstructures which develop specific functions of a connection between the motory unity and the tendon system. These formations ty ambient such as the one assured by proteoglicanic matrix in which perform the nervous formations wich are appointed to the peripheric control of the rnyotendon jointing. The morphological research led on a level of the myotendon jointings in normal conditions and in the course of insertional pathologia, has displayed howat an insertional level, it takes place deep structural changes characterized by progressive loss of the visco-elasticity . These dates have been put in relation to study of the elbow and wrist joints, in normal conditions and in course of 'tennis elbow'. In particular it has been inquired, in isokinetic, the relation of force of / the 'motor muscles' which control the motory unities of the elbow and wrist joints. In has been observed significative alteration of case control in the peak torque ratio (%) of the an d flex muscles of the wrist (80 vs 40) in the relation of pronators/supinators (138 vs 88). The results of this study suggest how at the base of “tennis elbow' there are biological and biomechanical conditions which determine the arising of pathologia, they condition the evolution and constitute the potential 'target' of the therapy

The Worldwide Spread, Success, and Impact of Ragweed (Ambrosia spp.)

The Ambrosia species represent one of the most problematic groups of invasive weeds around the world. The ease with which they are introduced and spread in new countries, their generalist ecological requirements, and functional traits facilitate their invasion and subsequent naturalization in new areas. All of these aspects contribute to increasing their global social and economic impact, which is mostly related to pollen allergy. Here we analyze available scientific publications about Ambrosia artemisiifolia, A. psilostachya, A. tenuifolia, and A. trifida, with the aim of defining the current level of knowledge and summarizing important data that are currently scattered throughout the literature. Specifically, we analyzed the following: (1) their current global distribution and current stage of invasion; (2) traits and requirements promoting their introduction, reproductive success, and adaptation to climate and environment in the nonnative range; as well as (3) current knowledge about allergens and elements increasing their impact

Cellular and molecular biology of cancer stem cells in melanoma : possible therapeutic implications

Malignant melanoma is a tumor characterized by a very high level of heterogeneity, responsible for its malignant behavior and ability to escape from standard therapies. In this review we highlight the molecular and biological features of the subpopulation of cancer stem cells (CSCs), well known to be characterized by self-renewal properties, deeply involved in triggering the processes of tumor generation, metastasis, progression and drug resistance. From the molecular point of view, melanoma CSCs are identified and characterized by the expression of stemness markers, such as surface markers, ATP-binding cassette (ABC) transporters, embryonic stem cells and intracellular markers. These cells are endowed with different functional features. In particular, they play pivotal roles in the processes of tumor dissemination, epithelial-to-mesenchymal transition (EMT) and angiogenesis, mediated by specific intracellular signaling pathways; moreover, they are characterized by a unique metabolic reprogramming. As reported for other types of tumors, the CSCs subpopulation in melanoma is also characterized by a low immunogenic profile as well as by the ability to escape the immune system, through the expression of a negative modulation of T cell functions and the secretion of immunosuppressive factors. These biological features allow melanoma CSCs to escape standard treatments, thus being deeply involved in tumor relapse. Targeting the CSCs subpopulation is now considered an attractive treatment strategy; in particular, combination treatments, based on both CSCs-targeting and standard drugs, will likely increase the therapeutic options for melanoma patients. The characterization of CSCs in liquid biopsies from single patients will pave the way towards precision medicine

Anticancer properties of tocotrienols : a review of cellular mechanisms and molecular targets

Vitamin E is composed of two groups of compounds: \u3b1-, \u3b2-, \u3b3-, and \u3b4-tocopherols (TPs), and the corresponding unsaturated tocotrienols (TTs). TTs are found in natural sources such as red palm oil, annatto seeds, and rice bran. In the last decades, TTs (specifically, \u3b3-TT and \u3b4-TT) have gained interest due to their health benefits in chronic diseases, based on their antioxidant, neuroprotective, cholesterol-lowering, anti-inflammatory activities. Several in vitro and in vivo studies pointed out that TTs also exert a significant antitumor activity in a wide range of cancer cells. Specifically, TTs were shown to exert antiproliferative/proapoptotic effects and to reduce the metastatic or angiogenic properties of different cancer cells; moreover, these compounds were reported to specifically target the subpopulation of cancer stem cells, known to be deeply involved in the development of resistance to standard therapies. Interestingly, recent studies pointed out that TTs exert a synergistic antitumor effect on cancer cells when given in combination with either standard antitumor agents (i.e., chemotherapeutics, statins, \u201ctargeted\u201d therapies) or natural compounds with anticancer activity (i.e., sesamin, epigallocatechin gallate (EGCG), resveratrol, ferulic acid). Based on these observations, different TT synthetic derivatives and formulations were recently developed and demonstrated to improve TT water solubility and to reduce TT metabolism in cancer cells, thus increasing their biological activity. These promising results, together with the safety of TT administration in healthy subjects, suggest that these compounds might represent a new chemopreventive or anticancer treatment (i.e., in combination with standard therapies) strategy. Clinical trials aimed at confirming this antitumor activity of TTs are needed

Unraveling the molecular mechanisms and the potential chemopreventive/therapeutic properties of natural compounds in melanoma

Melanoma is the most fatal form of skin cancer. Current therapeutic approaches include surgical resection, chemotherapy, targeted therapy and immunotherapy. However, these treatment strategies are associated with development of drug resistance and severe side effects. In recent years, natural compounds have also been extensively studied for their anti-melanoma effects, including tumor growth inhibition, apoptosis induction, angiogenesis and metastasis suppression and cancer stem cell elimination. Moreover, a considerable number of studies reported the synergistic activity of phytochemicals and standard anti-melanoma agents, as well as the enhanced effectiveness of their synthetic derivatives and novel formulations. However, clinical data confirming these promising effects in patients are still scanty. This review emphasizes the anti-tumor mechanisms and potential application of the most studied natural products for melanoma prevention and treatment

Diversity of dermal fibroblasts as major determinant of variability in cell reprogramming

Induced pluripotent stem cells (iPSCs) are adult somatic cells genetically reprogrammed to an embryonic stem cell-like state. Notwithstanding their autologous origin and their potential to differentiate towards cells of all three germ layers, iPSC reprogramming is still affected by low efficiency. As dermal fibroblast is the most used human cell for reprogramming, we hypothesize that the variability in reprogramming is, at least partially, because of the skin fibroblasts used. Human dermal fibroblasts harvested from five different anatomical sites (neck, breast, arm, abdomen and thigh) were cultured and their morphology, proliferation, apoptotic rate, ability to migrate, expression of mesenchymal or epithelial markers, differentiation potential and production of growth factors were evaluated in vitro. Additionally, gene expression analysis was performed by real-time PCR including genes typically expressed by mesenchymal cells. Finally, fibroblasts isolated from different anatomic sites were reprogrammed to iPSCs by integration-free method. Intriguingly, while the morphology of fibroblasts derived from different anatomic sites differed only slightly, other features, known to affect cell reprogramming, varied greatly and in accordance with anatomic site of origin. Accordingly, difference also emerged in fibroblasts readiness to respond to reprogramming and ability to form colonies. Therefore, as fibroblasts derived from different anatomic sites preserve positional memory, it is of great importance to accurately evaluate and select dermal fibroblast population prior to induce reprogramming