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1.
Taiwan J Obstet Gynecol ; 59(4): 586-589, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32653134

ABSTRACT

OBJECTIVE: Mature cystic teratoma is a common benign ovarian tumor. But extragonadal teratomas are very rare. They mainly occur in the midline structure of the body. Uterine teratomas are extremely rare with only few reports. The diagnosis was mainly based on the operative findings. We report a case of uterine mature teratoma in a 37 year-old woman who was diagnosed before the operation. We also review the literature about this exceptional presentation. CASE REPORT: We report a case of uterine teratoma that was initially diagnosed as a uterine tumor under ultrasound examination. But teratoma was highly suspected preoperatively by the abdominal CT scan. She underwent tumor excision via laparotomy. The operative finding and the histological examination confirms the diagnosis of primary uterine teratoma. CONCLUSION: Preoperatively diagnosis of uterine teratoma was difficult. Although there are no gold standard to treat the uterine teratoma, the majority of the treatment choice is surgery. The prognosis of this unusual disease is relatively good in benign lesions.


Subject(s)
Teratoma/diagnosis , Uterine Neoplasms/diagnosis , Adult , Diagnosis, Differential , Female , Humans , Teratoma/pathology , Teratoma/surgery , Ultrasonography , Uterine Neoplasms/pathology , Uterine Neoplasms/surgery
2.
Cell Physiol Biochem ; 41(5): 1851-1864, 2017.
Article in English | MEDLINE | ID: mdl-28376477

ABSTRACT

BACKGROUND: Osteopontin (OPN) is highly expressed in colorectal cancer (CRC) and is associated with disease progression in vivo. High levels of OPN have been demonstrated to predict low survival rates in CRC. Autophagy is a process of self-digestion, which is thought to play a significant role in carcinogenesis. However, the mechanisms of OPN's effects on CRC cell autophagy have not been elucidated. Therefore, we aimed to investigate possible mechanisms of OPN's effects on CRC autophagy. METHODS: HCT116 cell proliferation, apoptosis, and migration and invasion ability were identified by cell counting k¡t-8 assay, flow cytometry, wound healing assay, and transwell chamber invasion assay, respectively. The ratios of proteins LC3-II/LC3-I, P62, and Atg7 were analyzed by Western-blot. Expressions of Beclin-1, Atg4b, Bnip3, and Vps34, both in transcriptional and translational levels, were analyzed and compared by RT-PCR and Western blot. Immunofluorescence and co-focusing experiments were used to investigate the formation of autophagosomes. RESULTS: The results showed that OPN can promote cell proliferation, migration, and invasion, as well as inhibit cell apoptosis. It was also demonstrated that OPN could inhibit cell autophagy. Further experiments revealed that the inhibitory effect of OPN on autophagy could be reversed by blocking the p38 MAPK pathway in HCT116 cells. CONCLUSION: OPN is involved in HCT116 cell progression and is capable of inhibiting cell autophagy possibly by activating the p38 MAPK signaling pathway, implying that OPN could be a potential novel molecular therapeutic biomarker in patients with CRC.


Subject(s)
Apoptosis , Autophagy , Cell Movement , Colorectal Neoplasms/metabolism , MAP Kinase Signaling System , Neoplasm Proteins/metabolism , Osteopontin/metabolism , p38 Mitogen-Activated Protein Kinases/metabolism , Cell Line, Tumor , Colorectal Neoplasms/genetics , Humans , Neoplasm Invasiveness , Neoplasm Proteins/genetics , Osteopontin/genetics , p38 Mitogen-Activated Protein Kinases/genetics
4.
ASAIO J ; 50(4): 294-300, 2004.
Article in English | MEDLINE | ID: mdl-15307536

ABSTRACT

Mechanical artificial heart valves rely on reverse flow to close their leaflets. This mechanism creates regurgitation and water hammer effects that may form cavitations, damage blood cells, and cause thromboembolism. This study analyzes closing mechanisms of monoleaflet (Medtronic Hall 27), bileaflet (Carbo-Medics 27; St. Jude Medical 27; Duromedics 29), and trileaflet valves in a circulatory mock loop, including an aortic root with three sinuses. Downstream flow field velocity was measured via digital particle image velocimetry (DPIV). A high speed camera (PIVCAM 10-30 CCD video camera) tracked leaflet movement at 1000 frames/s. All valves open in 40-50 msec, but monoleaflet and bileaflet valves close in much less time (< 35 msec) than the trileaflet valve (>75 msec). During acceleration phase of systole, the monoleaflet forms a major and minor flow, the bileaflet has three jet flows, and the trileaflet produces a single central flow like physiologic valves. In deceleration phase, the aortic sinus vortices hinder monoleaflet and bileaflet valve closure until reverse flows and high negative transvalvular pressure push the leaflets rapidly for a hard closure. Conversely, the vortices help close the trileaflet valve more softly, probably causing less damage, lessening back flow, and providing a washing effect that may prevent thrombosis formation.


Subject(s)
Aortic Valve , Heart Valve Prosthesis , Acceleration , Electronic Data Processing , Glycerol , Heart Valve Prosthesis/standards , Humans , Mechanics , Photography , Prosthesis Design , Rheology , Solutions , Time Factors
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