No abstract

Phosphatase PRL-3 expression is positively associated to acute myeloid leukemia (AML) progression and drug resistance. SH3-domain-binding glutamic acid-rich protein-like protein (SH3BGRL), a downstream effector of PRL-3, plays a tumor suppressive role in solid tumors, but it remains elusive in AML. Here, we followed up and validated the relevance of SH3BGRL expression to AML progression in 116 cases. Results showed that SH3BGRL is down-regulated in 62.37% AML cases with poor prognosis. Cases with positive response to therapy accompanies with SH3GRL expression restoration. Mechanistically, SH3BGRL down-regulation promotes AML cell cycle progression and enhances the anti-apoptotic ability to drug cytotoxicity. While ectopic SH3BGRL blocks AML cell cycle and proliferation to sensitize them to therapeutic drugs via apoptosis. Xenograft assays further confirmed the suppressive role of SH3BGRL in leukemogenesis. Thus, our results demonstrated that SH3BGRL is a novel crucial player in AML progression and could be both a potential diagnostic and prognostic marker.

The aim of the present study was to investigate the value of systemic [F]fluorodeoxyglucose positron emission tomography (PET)/computed tomography (CT) in the diagnosis and differential diagnosis of aplastic anemia (AA). Systemic PET/CT imaging results of 24 patients diagnosed with AA in The First Affiliated Hospital of Sun Yat-Sen University between May 2011 and August 2014 were retrospectively analyzed and compared with results from healthy individuals and patients with acute leukemia (AL) or myelodysplastic syndrome (MDS) in the same period to summarize the PET/CT characteristics of patients with AA. Systemic PET/CT manifestations of the 24 patients with AA were classified into three types: Normal bone marrow metabolism, hypometabolism and hypometabolism complicated by focal hyperproliferation. Focal hyperproliferation was frequently identified in the vertebral body, breast bones and iliac bones. Bone marrow maximum standardized uptake values (SUV) of AA were associated, to certain extents, with the degree of proliferation and the bone marrow T/B cell ratio. The overall bone marrow SUV of AA were lower compared with those of healthy individuals and AL or patients with MDS, indicating hypometabolism. Considering the T/B cell ratio, systemic PET/CT manifestations of patients with AA are able to predict treatment responses to certain degrees. Systemic PET/CT is highly valuable in the diagnosis and differential diagnosis of AA, and may also indicate treatment responses.

No abstract

Although elevated CO2 (eCO2) in the atmosphere is one of the main factors influencing climate and ecosystem stability, less research on eCO2 in greenhouse soil systems has been conducted, despite their prevalence. In this article, phospholipid fatty acid (PLFA) profiling, 16S rRNA and Internally Transcribed Spacer (ITS) gene sequencing and high-throughput quantity polymerase chain reactions (HT-qPCRs) for 72 biogeochemical cycling-related genes were used to reveal the comprehensive responses of microbes to 23 days eCO2 fumigation in the soil of a tomato greenhouse. Our results indicated that eCO2 significantly increased microbial biomass (p < 0.05). The fungal community was more susceptible to eCO2 than the bacterial community; the fungal alpha diversity indices decreased significantly under eCO2 (p < 0.05) and the abundance of Ascomycota and its lower level taxa also increased significantly (p < 0.01). The absolute abundance of numerous C, N, P, S and methane cycling related genes increased significantly (p < 0.05) under eCO2. Furthermore, the microbial community structure and function were correlated with certain measured plant characteristics. Hence, the microbial ecosystem of the tomato greenhouse soil system was stimulated under eCO2. These results contribute to a greater understanding of how eCO2 in the atmosphere affects terrestrial ecosystem stability.