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1.
Tumour Biol ; 37(11): 14873-14883, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27644245

RESUMEN

Fatty acid-binding protein 5 (FABP5) was found in our previous study to be a potential biomarker for lymph node metastasis of cervical cancer. However, the roles of FABP5 in cervical cancer remain unclear. In the present study, FABP5 expression was found to be significantly upregulated in cervical cancer tissues, and high FABP5 expression was significantly correlated with lymph node metastasis, lymphovascular space invasion, the International Federation of Gynecology and Obstetrics (FIGO) stage, and tumor size. Moreover, FABP5 was an independent factor for poor prognosis in cervical cancer patients. Silencing of FABP5 inhibited cell proliferation, colony formation, cell migration, and invasion in vitro. Furthermore, FABP5 silencing significantly reduced tumor growth and lung metastases in a murine allograft model in vivo. In addition, FABP5 silencing decreased the expression of matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9) in vitro and in vivo. Collectively, these findings indicated that FABP5 plays an important role in the carcinogenesis and metastasis of cervical cancer, and FABP5 may be a novel predictor for prognostic assessment of cervical cancer patients.


Asunto(s)
Biomarcadores de Tumor/genética , Carcinogénesis/genética , Proliferación Celular/genética , Proteínas de Unión a Ácidos Grasos/genética , Neoplasias del Cuello Uterino/patología , Adulto , Animales , Línea Celular Tumoral , Movimiento Celular/genética , Femenino , Células HeLa , Humanos , Neoplasias Pulmonares/secundario , Metástasis Linfática , Metaloproteinasa 2 de la Matriz/biosíntesis , Metaloproteinasa 9 de la Matriz/biosíntesis , Ratones , Ratones Desnudos , Invasividad Neoplásica/genética , Pronóstico , Interferencia de ARN , ARN Interferente Pequeño , Neoplasias del Cuello Uterino/mortalidad
2.
Int J Gynecol Cancer ; 26(7): 1264-73, 2016 09.
Artículo en Inglés | MEDLINE | ID: mdl-27643649

RESUMEN

OBJECTIVE: The aim of the study was to investigate the long-term oncological outcomes of laparoscopic radical hysterectomy (LRH) and abdominal radical hysterectomy (ARH) for treatment of stage IA2 to IIA2 cervical cancer. METHODS: We matched stage IA2 to IIA2 cervical cancer patients with known risk factors for recurrence who underwent ARH or LRH. RESULTS: After matching, a total of 203 patient pairs (LRH-ARH) were included. The LRH and ARH group had similar 5-year recurrence-free survival (RFS) rates (91.3% vs 90.4%, P = 0.83) and overall survival (OS) rates (93.2% vs 92.1%, P = 0.94). Patients with different tumor size (≤2, 2-4, >4 cm) had similar 5-year OS and RFS. Even in patients with pelvic lymph node metastasis, the 5-year RFS (69.20% vs 69.20%, P = 0.87) and OS (77.4% vs 76.3%, P = 0.83) did not differ statistically between the 2 groups. The LRH and ARH group had similar mean time to recurrence (16.29 vs 22.15 months, P = 0.68) and pattern of recurrence (P = 0.63). Compared with ARH, LRH resulted in significantly shorter operating time, less blood loss, and shorter hospital stay. The intraoperative complications rate was similar between the 2 groups (P = 0.72). The rate of postoperative complications was significantly lower in the LRH group than in the ARH group (P = 0.004). CONCLUSIONS: Laparoscopic radical hysterectomy was associated with fewer operating time, blood loss, postoperative complication, and earlier recovery. Laparoscopic radical hysterectomy is an oncologically safe alternative to ARH.


Asunto(s)
Carcinoma/cirugía , Histerectomía/estadística & datos numéricos , Complicaciones Posoperatorias/epidemiología , Neoplasias del Cuello Uterino/cirugía , Adulto , Carcinoma/mortalidad , China/epidemiología , Estudios de Cohortes , Femenino , Humanos , Histerectomía/efectos adversos , Histerectomía/métodos , Laparoscopía/efectos adversos , Laparoscopía/estadística & datos numéricos , Persona de Mediana Edad , Complicaciones Posoperatorias/etiología , Neoplasias del Cuello Uterino/mortalidad
3.
Zhonghua Nan Ke Xue ; 19(6): 535-8, 2013 Jun.
Artículo en Zh | MEDLINE | ID: mdl-23862233

RESUMEN

OBJECTIVE: To investigate the clinicopathological characteristics, differential diagnosis and prognosis of testicular cellular fibroma. METHODS: We comprehensively analyzed the clinical presentation, histomorphology and immunohistochemistry of a case of testicular cellular fibroma, reviewed the relevant literature, and discussed its pathological features and differential diagnosis. RESULTS: A 30-year-old man presented with complaint of discomfort and painless enlargement in the right testis. The tumor was found to be a testicular fibroma characterized by a solid, thickly or thinly encapsulated, circumscribed and gray-white mass. Microscopically, fusiform cells were arranged into a storiform and herringbone pattern or fascicles. The tumor exhibited a great deal of cellularity and no nuclear polymorphisms, with a mitotic rate of 0-1/10 HP. Immunohistochemistry showed that the tumor cells were positive for Vimentin, patchily positive for S-100 and SMA, but negative for Desmin, alpha-inhibin, CD34 and CD99. The positive rate of Ki-67 was less than 1%. CONCLUSION: Testicular cellular fibroma is a rare testicular sex cord stromal tumor, pathologically resembling its ovarian counterpart. It can be distinguished from other testicular spindle cell tumors by morphology and immunohistochemical staining. For the treatment of testicular cellular fibroma, surgical resection often has a good prognosis.


Asunto(s)
Fibroma/patología , Neoplasias Testiculares/patología , Adulto , Humanos , Inmunohistoquímica , Masculino
4.
Cardiol J ; 26(5): 584-593, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-29611167

RESUMEN

BACKGROUND: To study the protein profile of the serum exosomes of patients with coronary artery aneurysms (CAA) caused by Kawasaki disease (KD). METHODS: Two-dimensional electrophoresis (2-DE) was used to identify proteins from the exosomes of serum obtained from children with CAA caused by KD, as well as healthy controls. Differentially expressed proteins were identified using matrix-assisted laser desorption/ionization time-of-flight/timeof-flight mass spectrometry (MALDI-TOF/TOF MS) analysis. RESULTS: Thirty two differentially expressed proteins were identified (18 up-regulated and 14 downregulated) from serum exosomes of children with CAA and were compared to healthy controls. The expression levels of 4 proteins (TN, RBP4, LRG1, and APOA4) were validated using Western blotting. Classification analysis and protein-protein network analysis showed that they are associated with multiple functional groups, including host immune response, inflammation, apoptotic process, developmental process, and biological adhesion process. CONCLUSIONS: These findings establish a comprehensive proteomic profile of serum exosomes from children with CAA caused by KD, and provide additional insights into the mechanisms of CAA caused by KD.


Asunto(s)
Aneurisma Coronario/sangre , Exosomas/química , Síndrome Mucocutáneo Linfonodular/complicaciones , Proteínas/análisis , Proteómica , Apolipoproteínas A/sangre , Estudios de Casos y Controles , Aneurisma Coronario/diagnóstico , Aneurisma Coronario/etiología , Electroforesis en Gel Bidimensional , Exosomas/ultraestructura , Glicoproteínas/sangre , Humanos , Lectinas Tipo C/sangre , Síndrome Mucocutáneo Linfonodular/diagnóstico , Mapas de Interacción de Proteínas , Proteínas Plasmáticas de Unión al Retinol/análisis , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción
5.
Nan Fang Yi Ke Da Xue Xue Bao ; 29(2): 228-31, 2009 Feb.
Artículo en Zh | MEDLINE | ID: mdl-19246285

RESUMEN

OBJECTIVE: To construct a recombinant lentivirus harboring RNA interference sequence targeting mouse CD99 antigen-like 2 (mCD99L2) gene and observe its infection efficiency of 293FT cells. METHODS: Four pairs of small interfering RNAs (siRNAs) targeting mCD99L2 cDNA were designed, synthesized and linked to the lentivirus vector SD1259 to construct the lentivirus shuttle plasmids. After sequencing, the 4 lentivirus shuttle plasmids were transfected into 293FT cells in the presence of packaging plasmids. Forty-eight hours later, the supernatant was collected and the titer and infection efficiency of the recombinant lentivirus were determined according to the expression of the reporter gene enhanced green fluorescent protein (EGFP) under fluorescent microscope. RESULTS: DNA sequencing demonstrated that mCD99L2 siRNAs were successfully cloned to the lentiviral vector SD1259. The titer of concentrated virus was 1x10(7)/ml in the supernatant of the infected cells. CONCLUSION: The recombinant lentivirus containing siRNA targeting mCD99L2 gene has been successfully constructed, which provide the basis for future establishment of visualized cell model and animal model of Hodgkin's lymphoma.


Asunto(s)
Antígenos CD/genética , Vectores Genéticos , Enfermedad de Hodgkin/patología , Lentivirus/genética , ARN Interferente Pequeño/genética , Antígeno 12E7 , Animales , Secuencia de Bases , ADN Complementario/genética , Proteínas Fluorescentes Verdes/genética , Proteínas Fluorescentes Verdes/metabolismo , Lentivirus/metabolismo , Ratones , Datos de Secuencia Molecular , Interferencia de ARN , Proteínas Recombinantes/genética , Células Tumorales Cultivadas
6.
Nan Fang Yi Ke Da Xue Xue Bao ; 28(4): 572-5, 2008 Apr.
Artículo en Zh | MEDLINE | ID: mdl-18495593

RESUMEN

OBJECTIVE: To compare the efficacy of nuclear microarray combined with fluorescence in situ hybridization (FISH) and immunohistochemistry in detecting ALK gene translocation and ALK fusion protein in anaplastic large cell lymphoma (ALCL). METHODS: ALK gene translocation and ALK fusion protein in 17 paraffin-embedded ALCL specimens were detected using nuclear microarray combined with FISH and immunohistochemical straining, respectively. RESULTS: The expression of ALK fusion protein was detected immunohistochemically with ALK antibody in 8 of the 17 specimens of systemic ALCL, including 4 with both nuclear and cytoplasmic positivity and 4 with only cytoplasmic positivity. Dual-color FISH identified 6 positive specimens, including the 4 specimens with both nuclear and cytoplasmic positivity as identified immunohistochemically, and 2 with immunohistochemical cytoplasmic positivity. FISH yielded negative results for the 2 specimens with immunohistochemical cytoplasmic positivity. CONCLUSION: Nuclear microarray combined with FISH eliminated the cytoplasmic interference of the results of conventional FISH and provides a high-throughput platform for clinical detection with greater specificity than immunohistochemistry.


Asunto(s)
Hibridación Fluorescente in Situ/métodos , Linfoma Anaplásico de Células Grandes/genética , Proteínas Tirosina Quinasas/genética , Translocación Genética , Adolescente , Adulto , Anciano , Quinasa de Linfoma Anaplásico , Niño , Preescolar , Femenino , Humanos , Inmunohistoquímica , Linfoma Anaplásico de Células Grandes/enzimología , Linfoma Anaplásico de Células Grandes/patología , Masculino , Análisis por Micromatrices/métodos , Persona de Mediana Edad , Adhesión en Parafina , Proteínas Tirosina Quinasas Receptoras , Reproducibilidad de los Resultados , Adulto Joven
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