Development and validation of an online calculator to predict the pathological nature of colorectal tumors.

Background: No single endoscopic feature can reliably predict the pathological nature of colorectal tumors (CRTs).

Aim: To establish and validate a simple online calculator to predict the pathological nature of CRTs based on white-light endoscopy.

Methods: This was a single-center study.

PTPMT1 regulates mitochondrial death through the SLC25A6-NDUFS2 axis in pancreatic cancer cells.

Pancreatic ductal adenocarcinoma is a highly malignant cancer with poor prognosis, for which effective therapeutic strategies are urgently needed. The dual-specificity phosphatase PTPMT1 is localized in mitochondria and highly expressed in various cancers. Here, we investigated the function of PTPMT1 in pancreatic ductal adenocarcinoma.

MAC mediates mammary duct epithelial cell injury in plasma cell mastitis and granulomatous mastitis.

Unlabelled: Plasma cell mastitis (PCM) and granulomatous mastitis (GM) are common inflammatory nonbacterial mastitis (NBM). However, the pathogenesis of NBM is still unclear.

Methods: In this study, we statistically analyzed the pathological features of PCM and GM using pathological HE staining and tissue transmission electron microscopy.

CO or air cholangiography reduces the risk of post-ERCP cholangitis in patients with Bismuth type IV hilar biliary obstruction.

Background: Endoscopic biliary stenting by endoscopic retrograde cholangiopancreatography (ERCP) is the most common form of palliation for malignant hilar obstruction. However, ERCP in such cases is associated with a risk of cholangitis. The incidence of post-ERCP cholangitis is particularly high in Bismuth type IV hilar obstruction, and this risk is further increased when the contrast injected for cholangiography is not drained.

Molecular defect-containing bilayer graphene exhibiting brightened luminescence.

The electronic structure of bilayer graphene can be altered by creating defects in its carbon skeleton. However, the natural defects are generally heterogeneous. On the other hand, rational bottom-up synthesis offers the possibility of building well-defined molecular cutout of defect-containing bilayer graphene, which allows defect-induced modulation with atomic precision.

Malignant glomus tumor of the intestinal ileum with multiorgan metastases: A case report and review of literature.

Background: Glomus tumors (GTs) are rare mesenchymal neoplastic lesions derived from cells of the glomus body. GTs rarely occurs in the visceral organs, where there may be few or no glomus bodies, and the majority of GTs are benign, rarely demonstrating aggressive or malignant behavior and histological features.

Case Summary: We report a patient with malignant GTs of the intestinal ileum with multiorgan metastases who was admitted due to moderate anemia.

[Niches and interspecific association of dominant shrimp species in the offshore waters of southern Zhejiang Province, China].

Based on data from November of 2015 (autumn), February (winter), May (spring), and August (summer) of 2016 in the offshore waters of southern Zhejiang Province, the relationships between major shrimps species were examined by niche breadth, niche overlap, variance ratio, chi-square test, association coefficient and species pair co-occurrence percentage. The results showed that temporal niche breadth of Atypopenaeus stenodactylu was the largest, spatial niche breadth of Solenocera crassicornis was the largest, and A. stenodactylu had the largest spatio-temporal niche breadth.

Molecular bilayer graphene.

Bilayer graphene consists of two stacked graphene layers bound together by van der Waals interaction. As the molecular analog of bilayer graphene, molecular bilayer graphene (MBLG) can offer useful insights into the structural and functional properties of bilayer graphene. However, synthesis of MBLG, which requires discrete assembly of two graphene fragments, has proved to be challenging.

MicroRNA-26a inhibits proliferation by targeting high mobility group AT-hook 1 in breast cancer.

Objectives: To investigate the crucial role of miR-26a in breast cancer and to validate whether miR-26a could regulate proliferation of breast cancer cells by targeting high mobility group AT-hook 1 (HMGA1).

Methods: Reverse transcription-polymerase chain reaction (RT-PCR) was used to quantify the expression levels of miR-26a in breast cancer and adjacent non-cancerous breast tissues. MTT, cell migration and invasion assay were carried out to characterize the miR-26a function.