Publications by authors named "Jinghong Peng"

Ependymoma is the third most common pediatric tumor with posterior fossa group A (PFA) being its most aggressive subtype. Ependymomas are generally refractory to chemotherapies and thus lack any effective treatment. Here, we report that elevated expression of CXorf67 (chromosome X open reading frame 67), which frequently occurs in PFA ependymomas, suppresses homologous recombination (HR)-mediated DNA repair.

View Article and Find Full Text PDF

Long-distance gas pipelines generally have complex, undulating sections. Trapped air pockets are often present at the high points or ends of pipelines. This article carries out an experimental research to figure out the transient changes.

View Article and Find Full Text PDF
Article Synopsis
  • Follicular lymphoma (FL) is a common type of lymphoma in the U.S. and Europe, and its diagnosis and grading have not changed much according to the latest WHO classification updates.
  • FL exhibits a wide range of biological and histopathological variations, making some cases hard to identify due to their unique features or being rare variants.
  • This text discusses several unusual FL cases to increase awareness of the diverse histopathological characteristics, including FL variants with Castleman-like changes and those involving specific mutations or virus-related features.
View Article and Find Full Text PDF
Article Synopsis
  • - Prolymphocytic transformation refers to a situation in chronic lymphocytic leukemia/small lymphocytic lymphoma where over 55% of prolymphocytes are found in peripheral blood, and it can also occur in other lymphomas like mantle cell lymphoma and rarely in splenic marginal zone lymphoma (SMZL).
  • - This study presents two unique cases of splenic B-cell lymphomas in a leukemic phase, both classified as SMZL with prolymphocytic transformation, with one case mimicking B-prolymphocytic leukemia (B-PLL).
  • - Notably, both lymphomas expressed cyclin D1 without the typical genetic marker t(11; 14), raising the possibility of
View Article and Find Full Text PDF

Background: Partial monosomy 21 is a rare finding with variable sizes and deletion breakpoints, presenting with a broad spectrum of phenotypes.

Case Presentation: We report a 10-month-old boy with short stature, minor anomalies and mild motor delay. The patient had a monosomy 21 and duplication of the 21q22.

View Article and Find Full Text PDF
Article Synopsis
  • - The study discusses a rare case of a 15-year-old girl diagnosed with primary mediastinal large B-cell lymphoma (PMLBCL), which is known for its aggressiveness and specific characteristics.
  • - Genetic testing revealed "double-hit" (DH) abnormalities involving the MYC and BCL6 genes, expanding the understanding of how DH events can occur in PMLBCL, where such associations were previously unreported.
  • - The findings highlight the importance of cytogenetic testing for DH abnormalities in aggressive large B-cell lymphomas to improve diagnosis and treatment options.
View Article and Find Full Text PDF

The status of human epidermal growth factor receptor 2 (HER2, ERBB2) determines the eligibility of breast cancer patients to receive HER2-targeted therapy. The majority of HER2 testing in the U.S.

View Article and Find Full Text PDF

A series of fluorene derivatives end-capped with diphenylamino and oxadiazolyl were synthesized, and their photophysical and electrochemical properties are reported. Aggregation-induced emission (AIE) effects were observed for the materials, and bipolar characteristics of the molecules are favored with measurement of carrier mobility and calculation of molecular orbitals using density functional theory (DFT). Using the fluorene derivatives as emitting-layer, nondoped organic light-emitting devices (OLEDs) have been fabricated by spin-coating in the configuration ITO/PEDOT:PSS(35 nm)/PVK(15 nm)/PhN-OF(n)-Oxa(80 nm)/SPPO13(30 nm)/Ca(8 nm)/Al(100 nm) (n = 2-4).

View Article and Find Full Text PDF

Background And Aim: Diagnosis of pancreatic malignancy is often based on cytological specimens collected by endoscopic ultrasound guided fine needle aspiration (EUS FNA). Several factors can decrease sensitivity of EUS FNA for pancreatic cancer: well-differentiated tumors, pancreatitis, blood, necrosis and slides with low cellularity. The objective of this study is to report on the use of fluorescence in situ hybridization (FISH) analysis combined with cytology in pancreatic masses.

View Article and Find Full Text PDF

Background: Genomic microarrays have been used as the first-tier cytogenetic diagnostic test for patients with developmental delay/intellectual disability, autism spectrum disorders and/or multiple congenital anomalies. The use of SNP arrays has revealed regions of homozygosity in the genome which can lead to identification of uniparental disomy and parental consanguinity in addition to copy number variations. Consanguinity is associated with an increased risk of birth defects and autosomal recessive disorders.

View Article and Find Full Text PDF

Introduction: Oxygen exposure plays an important role in the pathogenesis of bronchopulmonary dysplasia (BPD). The phosphodiesterase inhibitor pentoxifylline (PTX) has anti-inflammatory and antifibrotic effects in multiple organs. It was hypothesized that PTX would have a protective effect on hyperoxia-induced lung injury (HILI).

View Article and Find Full Text PDF
Article Synopsis
  • The Smad2/3 pathway is crucial for how TGF-beta1 prevents branching morphogenesis and promotes CTGF expression in developing lungs.
  • Researchers studied how inhibiting the JNK pathway affects TGF-beta1's ability to activate Smad2 and influence lung development in mouse embryos.
  • Results showed that JNK inhibition enhances Smad2 activity, decreases normal branching, promotes CTGF expression, and causes cell death, suggesting that the JNK pathway may counteract the effects of TGF-beta1 on lung development.
View Article and Find Full Text PDF

Background: Acute episodes of hypoxemia in ventilated preterm infants are triggered by changes in ventilation, lung volume (LV) and respiratory system compliance (C(RS)) that are not prevented by conventional synchronized intermittent mandatory ventilation (SIMV).

Objective: To assess in a rabbit model of episodic hypoxemia the individual and combined efficacy of targeted tidal volume (V(T)) and minute ventilation (V'(E)) by automatic adjustment of peak inspiratory pressure (PIP) and ventilator rate, respectively.

Methods: Six young New Zealand white rabbits were ventilated with SIMV, targeted V(T), targeted V'(E), and combined targeted V'(E) + V(T) in random sequence.

View Article and Find Full Text PDF

High tidal volume (V(T)) ventilation plays a key role in ventilator induced lung injury and bronchopulmonary dysplasia. However, little is known about the effect of high V(T) on expression of growth factors that are critical to lung development. In a previous study, we demonstrated that connective tissue growth factor (CTGF) inhibits branching morphogenesis.

View Article and Find Full Text PDF
Article Synopsis
  • Transforming growth factor-beta1 (TGF-beta1) is identified as a key negative regulator of lung branching morphogenesis, influencing growth processes in developing lungs.
  • Researchers found that TGF-beta1 not only inhibits branching morphogenesis but also induces the expression of connective tissue growth factor (CTGF), which mediates this inhibitory effect.
  • The study also revealed that inhibiting the TGF-beta signaling pathway with SB431542 could reverse the effects of TGF-beta1 and promote normal lung branching, highlighting the role of the TbetaRI/ALK-5-dependent Smad2 signaling pathway in this process.
View Article and Find Full Text PDF