Glioblastoma multiforme (GBM) is the commonest primary malignant brain tumor and has a remarkably weak prognosis. According to the aggressive form of GBM, understanding the accurate molecular mechanism associated with GBM pathogenesis is essential. Growth differentiation factor 15 (GDF‐15) belongs to transforming growth factor‐β superfamily with important roles to control biological processes. It affects cancer growth and progression, drug resistance, and metastasis. It also can promote stemness in many cancers, and also can stress reactions control, bone generation, hematopoietic growth, adipose tissue performance, and body growth, and contributes to cardiovascular disorders. The role GDF‐15 to develop and progress cancer is complicated and remains unclear. GDF‐15 possesses tumor suppressor properties, as well as an oncogenic effect. GDF‐15 antitumorigenic and protumorigenic impacts on tumor development are linked to the cancer type and stage. However, the GDF‐15 signaling and mechanism have not yet been completely identified because of no recognized cognate receptor.
background. Stroke is the second leading cause of death and the most common debilitating neurological disorder worldwide. The ischemic injury causes inflammation and oxidative stress, and leads to apoptosis, necrosis and activation of autophagal pathways determining final infarct size. Melatonin, a hormone secreted by the pineal gland, is a small molecule that acts as a free radical scavenger, and performs antioxidant activities in several neurodegenerative diseases. Melatonin secretion reduces in aging due to pineal gland calcification and thus the calcification is a representative of reduced melatonin production. In this study, our aim was to evaluate the association of pineal gland calcification and stroke. Material and methods. An analytical cross sectional single center study was conducted. Pineal gland calcification was assessed by CT scan in 179 patients with ischemic stroke and 177 hospital controls. results. The mean age in the control and stroke groups were 58.18 and 61.2 years, respectively. Pineal gland calcification was found in 77.4% of subjects in the control group and 88.8% of the subjects in the stroke group. Pineal gland calcification, alone, was shown to significantly increase the risk of ischemic stroke (P=0.005; OR=2.3; 95% CI=1.2-4.1). Furthermore, after adjustment for diabetes mellitus, hypertension, hyper lipedema, gender, and age, there was still a significant association of pineal gland calcification with ischemic stroke (P=0.04; OR=2.0; 95% CI=1.0-3.9). conclusion. The evidence from the present study suggests that pineal gland calcification is associated with ischemic stroke.
Primitive neuroectodermal tumor (PNET) is a highly aggressive tumor and
mostly develops in children and young adults. PNETs of peripheral nerves
are uncommon. Ulnar nerve, in particular, is an extremely peculiar
origin for PNET and to the best of our knowledge only few
well-documented cases have been yet reported.
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