Abstract: The present disclosure relates to a newly discovered tumor marker for hepatocellular carcinoma (HCC) and related applications thereof in clinical detection. The tumor marker for HCC in the present disclosure is OIT3, which is abnormally expressed at low levels in HCC tissues and can be used in the diagnosis and treatment of HCC. The present application further relates to primer sequences of OIT3 as an HCC marker, which can be used as a reagent for the detection and diagnosis of HCC. The present disclosure can improve the accuracy, efficiency, and diagnosis of early HCC and is suitable for popularization in the clinical diagnosis of HCC.

Abstract: Provided are applications of an upstream Open Reading Frame (uORF) of a Phosphatase and Tensin homolog (PTEN) gene and a polypeptide coded by the same. A potential ORF of 96 bases (31aa-uORF) existing in the 5? UTR of the PTEN can code an oligopeptide of 31 amino acids (named PTEN-31aa) and plays an important role in the development and progression process of tumors. Provided is a new diagnostic and therapeutic method and a drug screening platform for PTEN expression regulation related diseases, in particular gliomas. Also provided is a polypeptide for treatment of PTEN expression regulation related diseases.

Abstract: The present disclosure describes drug-loaded nanoparticles for hepatic artery chemoembolization, wherein the drug-loaded nanoparticles are novel doxorubicin-loaded metal organic framework (MOF) nanoparticles and UiO-66/Bi2S3 nanocomposites. The preparation method of the drug-loaded nanoparticles includes the following steps: mixing UiO-66/Bi2S3 with DOX solution, stirring the resultant mixture overnight at 25° C.±5° C. in a dark environment, centrifuging the mixture, and washing with deionized water to obtain UiO-66/UiO-66/Bi2S3@DOX composite nanomaterials. The present disclosure adopts a “one-pot reaction” with a simple preparation process. The pH-reactive release performance of the MOF material indicates that the tumor tissue of hepatocellular carcinoma (HCC) has a lower pH than normal tissue, and the acidic tumor environment can induce the release of doxorubicin from the nanomaterials.

Abstract: A multi-organ repairing and transferring device without interrupting a blood flow includes a first perfusion bin, a second perfusion bin and a third perfusion bin which are configured for storing respective organs. A first pump is arranged on a first pipeline, two ends of the first pipeline are connected with the first perfusion bin and the second perfusion bin respectively, a second pump is arranged on a second pipeline, two ends of the second pipeline are connected with the first perfusion bin and the second perfusion bin respectively, a third pump is arranged on a third pipeline, two ends of the third pipeline are connected with the first perfusion bin and the third perfusion bin respectively, and a fourth pump is arranged on a fourth pipeline, two ends of the fourth pipeline are connected with the first perfusion bin and the third perfusion bin respectively.

Abstract: Disclosed is an ischaemia-free organ perfusion device and perfusion method. The perfusion device perfuses an isolated organ at normal temperature during whole transplantation, and comprises a first container, a second container, a first flow path, a second flow path, a third flow path and a fourth flow path. The perfusion device and the perfusion method are capable of maintaining the blood flow of the isolated organ during whole transplantation without interruption by machine perfusion, recovering the blood of the organ, effectively avoiding the interruption of blood supply for the organ during the whole transplantation, and improving the prognosis of organ transplantation.

Abstract: Disclosed are an in-vitro cardiopulmonary combined perfusion system and perfusion method. The in-vitro cardiopulmonary combined perfusion system includes an organ cabin, a circulation cabin, a control cabin, a simple breathing cabin, a display and control panel, and a base. The organ cabin is connected with the circulation cabin, the control cabin and the simple breathing cabin. The control cabin is connected with the display and control panel. The organ cabin, the circulation cabin, the control cabin, the simple breathing cabin, and the display and control panel are mounted on the base.

Abstract: The invention belongs to the field of research and development of genetic engineering antibody drugs, in particular, relates to a method for treating a tumor by administering Circ-CDH1. The Circ-CDH1 is a circular RNA Circ-CDH1 nucleic acid molecule or the protein Circ-CDH1-28 KD expressed by the circular RNA Circ-CDH1 nucleic acid molecule. In particular, a monoclonal antibody Anti-Circ-CDH1 is designed against Circ-CDH1-28 KD, which can specifically detect the content of a protein encoded by endogenous circular RNA Circ-CDH1, can remarkably inhibit invasion and metastasis of cells from tumors such as glioma, breast cancer and the like, and has wide application prospects in clinical detection of tumors and invasion and metastasis treatment.

Abstract: The present invention has a simple structure which is convenient in preparation and easy to use. Moreover, in combination with three-dimensional preoperative analysis and rapid molding technology, the present invention has a high customized precision and clinical applicability, and is cost-effective. Based on the three-dimensional preoperative analysis and 3d printing model, the problems of high technical difficulty and cost of the customized accurate implantation of acetabular cup prosthesis in the total hip arthroplasty can be effectively solved, so that the learning curve of operator can be shortened. The present invention can realize the customized accurate implantation of acetabular cup prosthesis without fitting the positioning guiding module with the articular surface area, so that the assisted positioning and assisted reaming depth determination are realized without removing the guiding module when the acetabulum is being reamed, thus the accuracy of the assisted positioning can be guaranteed.

Abstract: The present invention provides a method for three-dimensional reconstruction of fascicular structure of human peripheral nerve, which comprises the steps of: obtaining human peripheral nerve and preparing a peripheral nerve sample; immersing the peripheral nerve sample into a liquid; setting scan parameters of Micro-MRI, scanning the peripheral nerve sample by Micro-MRI, to acquire image data of the peripheral nerve sample in the liquid environment; and three-dimensional reconstructing a structural model of the peripheral nerve sample based on the image data. By means of the method according to the present invention, high-quality scanned images are obtained without destroying the morphology and physical and chemical properties of peripheral nerve, so as to obtain a precise three-dimensional visualization model of peripheral nerve fascicle.

Abstract: The present invention provides a method for establishing a biomimetic nerve graft model for nerve fascicles of the extremities, which comprises the steps of: establishing a database of fascicles structures from nerve fascicles of the extremities with an imaging technique; obtaining information of a defective nerve trunk to be repaired of the extremities; and matching and fitting the information of the defective nerve trunk to be repaired of the extremities with/to the data in the database of fascicles structures, to establish a biomimetic nerve graft model that conforms to the characteristics of fascicles microstructure for nerve fascicles of the defective nerve trunk. In the present invention, the imaging technique and clinical data are fully utilized, to establish a biomimetic nerve graft model conforming to the characteristics of fascicles microstructure for varying types of detects, thus providing more accurate model information for repair of nerve trunk defects in the extremities.

Abstract: The present invention has a simple structure which is convenient in preparation and easy to use. Moreover, in combination with three-dimensional preoperative analysis and rapid molding technology, the present invention has a high customized precision and clinical applicability, and is cost-effective. Based on the three-dimensional preoperative analysis and 3d printing model, the problems of high technical difficulty and cost of the customized accurate implantation of acetabular cup prosthesis in the total hip arthroplasty can be effectively solved, so that the learning curve of operator can be shortened. The present invention can realize the customized accurate implantation of acetabular cup prosthesis without fitting the positioning guiding module with the articular surface area, so that the assisted positioning and assisted reaming depth determination are realized without removing the guiding module when the acetabulum is being reamed, thus the accuracy of the assisted positioning can be guaranteed.

Abstract: The present invention relates to fields of clinical application of nerve defect repair and the medical three-dimensional (3D) printing technology, and provides an integrated visualization method for three-dimensional (3D) reconstruction of internal structure of human peripheral nerves. The method comprises the following steps: obtaining human peripheral nerves, preparing nerve specimens ex vivo by staining with an iodine preparation in combination with a freeze-drying method; scanning the pretreated peripheral nerves using Micro CT to acquire lossless two-dimensional images, and performing binarization processing to the two-dimensional images, then conducting image segmentation based on textural features to acquire images of nerve fascicles; finally, reconstructing the segmented images into a visualization model by using a supercomputer.