2.Giant myoepithelial carcinoma of the nuchal region: a case report and literature review.
Feng LIU ; Jiang CHANG ; Baoyan ZHU ; Lifang LU ; Jie NAN ; Fei HAN
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2023;37(7):578-581
Myoepithelioma, also known as malignant myoepithelioma, is a rare malignant tumor originating from myoepithelial cell. This article reports a patient with a huge tumor in the neck and left elbow who underwent fine needle aspiration under local anesthesia. The pathological diagnosis was a myoepithelioma. Under general anesthesia, giant tumors in the lower neck, posterior cranial fossa, neck, and left elbow were removed, and postoperative pathology showed that they were all myoepithelial tumors. Immunohistochemistry showed AE1/AE3 (+), P63 (+), CK7 (+), CK5 (+), and CD138 (+). The clinical characteristics and diagnosis and treatment process of this case are reported and relevant literature is reviewed.
Humans
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Myoepithelioma/pathology*
;
Immunohistochemistry
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Epithelial Cells
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Neck/pathology*
;
Carcinoma
3.Sarcomatoid Renal Cell Carcinoma.
Yeon Won PARK ; Jae Hyuk SHIN ; Hyun Sub CHO ; Moon Ki JO ; Min Suk KIM ; Su Whan LEE ; Chang Ho LEE ; Hang Ro PARK ; Hyun Moo LEE
Korean Journal of Urology 2003;44(12):1294-1297
Cases of sarcomatoid renal cell carcinoma are very rare. It has been known that sarcomatoid renal cell carcinoma is an epithelial cell variant that has been metaplastically transformed with a very poor prognosis. Diagnosis of sarcomatoid renal cell carcinoma is performed by examining a nephrectomy specimen to see if epithelial and sarcomatoid components are variously mixed together. Therefore, the aim of this paper is to report five cases of sarcomatoid renal cell carcinoma.
Carcinoma, Renal Cell*
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Diagnosis
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Epithelial Cells
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Nephrectomy
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Pathology
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Prognosis
4.The role of bronchial epithelial cells in airway hyperresponsiveness.
Xiao-Qun QIN ; Yang XIANG ; Chi LIU ; Yu-Rong TAN ; Fei QU ; Li-Hua PENG ; Xiao-Ling ZHU ; Ling QIN
Acta Physiologica Sinica 2007;59(4):454-464
It is commonly accepted that airway hyperresponsiveness (AHR) is a chronic airway inflammation although the exact mechanism of its pathogenesis is still unclear. In the past ten years, an epithelial defect hypothesis has gradually gained supports from the main stream. Airway epithelium is no longer considered only as a simple mechanic barrier but an active interface between the inner and outer environment. Bronchial epithelial cells play a critical role in maintenance of homeostasis in the airway local microenvironment through a wide range of physiologic functions including anti-oxidation, exocrine/endocrine secretions, mucus production and antigen presentation under health and stressed/inflamed/injured conditions. It is reasonably hypothesized that disruption of these functional processes or defects in airway epithelium integrity may be the initial steps leading to airway hyperresponsiveness such as in asthma and chronic obstructive pulmonary disease.
Animals
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Bronchi
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cytology
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Bronchial Hyperreactivity
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physiopathology
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Epithelial Cells
;
pathology
;
Humans
5.Relationship between apoptosis and E-cadherin expression in bronchial epithelium of smoking mouse.
Lifang, LIU ; Yonghui, YUAN ; Fang, LI ; Hongyun, LIU
Journal of Huazhong University of Science and Technology (Medical Sciences) 2003;23(3):216-8
To investigate whether apoptosis is associated with cell adhesion in bronchial epithelium, and whether it contributes to the kinetics of injury and repair of surface epithelia, this study was performed for E-cadherin expression by using immunohistochemistry technique and for apoptosis by TUNEL method. An animal model of smoking was used for this study. The results showed that epithelial cells with membrane anchored E-cadherin decreased remarkably at several time points during 6 months of exposure to smoke (P < 0.01) and then restored to normal level. This fluctuation was associated exclusively with the alteration in number of apoptotic cells (P < 0.01). There was no significant difference in activation of nuclear transcription factor NF-kappa B among groups (P > 0.05). All these suggested that apoptosis is associated with E-cadherin expression in bronchial epithelium of smoking mouse.
*Apoptosis
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Bronchi/metabolism
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Bronchi/*pathology
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Cadherins/analysis
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Cadherins/*biosynthesis
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Epithelial Cells/chemistry
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Epithelial Cells/metabolism
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Epithelial Cells/pathology
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Smoking/*adverse effects
6.Primary culture of mammary epithelial cells derived from human breast hypertrophy.
Yun XIA ; Ke GUO ; Jia-Ming SUN ; Jie YANG ; Ling-Yun XIONG
Chinese Journal of Plastic Surgery 2012;28(5):356-359
OBJECTIVETo investigate the primary culture of mammary epithelial cells derived from human breast hypertrophy.
METHODSMammary epithelial cells of human breast hypertrophy were isolated and cultured by the collagenase digestion method. The morphology observation and identification of the cultured cells were performed by inverted microscope observation, HE staining and cytokeratin immunohistochemical staining.
RESULTSMost of the cultured cells were pebbles-like or polygon under the inverted microscopy. Some had irregular form. They had typical island-like appearance during multiplication with close connection between the cells. The HE staining results showed the cytoplasm was stained pink or lilac, the nucleus was stained bluish violet and was round or oval in shape, with clearly visible chromosomes in dark blue. The cytokeratin immunohistochemical staining demonstrated the tissue-specific expression of cytokeratin 18 in epithelial cells by the cytoplasm stained claybank.
CONCLUSIONHigh purity of primary mammary epithelial cells derived from human breast hypertrophy can be obtained by the collagenase digestion method and conditioned medium.
Breast ; cytology ; pathology ; Cells, Cultured ; Epithelial Cells ; cytology ; Female ; Humans ; Hypertrophy ; pathology ; Primary Cell Culture ; methods
7.Mechanisms of Epithelial-Mesenchymal Transition of Peritoneal Mesothelial Cells During Peritoneal Dialysis.
Journal of Korean Medical Science 2007;22(6):943-945
A growing body of evidence indicates that epithelial-mesenchymal transition (EMT) of human peritoneal mesothelial cells (HPMC) may play an important role in the development and progression of peritoneal fibrosis during long-term peritoneal dialysis (PD) leading to failure of peritoneal membrane function. Here, we review our own observations and those of others on the mechanisms of EMT of HPMC and suggest potential therapeutic strategies to prevent EMT and peritoneal fibrosis during long-term PD. We found that high glucose and H2O2 as well as transforming growth factor-beta1 (TGF-beta1) induced EMT in HPMC and that high glucoseinduced EMT was blocked not only by inhibition of TGF-beta1 but also by antioxidants or inhibitors of mitogen-activated protein kinases (MAPK). Since MAPKs are downstream target molecules of reactive oxygen species (ROS), these data suggest that high glucose-induced generation of ROS and subsequent MAPK activation mediate high glucose-induced EMT in HPMC. We and others also observed that bone morphogenetic protein-7 (BMP-7) prevented EMT in HPMC. Glucose degradation products (GDP) were shown to play a role in inducing EMT. Involvement of a mammalian target of rapamycin (mTOR) in TGF-beta1-induced EMT has also been proposed in cultured HPMC. A better understanding of the precise mechanisms involved in EMT of HPMC may provide new therapeutic strategies for inhibiting peritoneal fibrosis in long-term PD patients.
Epithelial Cells/*pathology
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Fibrosis
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Humans
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Mesoderm/*pathology
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Peritoneal Dialysis/*adverse effects
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Peritoneum/*pathology
8.Pathogenesis of idiopathic pulmonary fibrosis: from initial apoptosis of epithelial cells to lung remodeling?
Hua-Liang JIN ; Jing-Cheng DONG
Chinese Medical Journal 2011;124(24):4330-4338
Idiopathic pulmonary fibrosis (IPF) is a progressive and often fatal form of interstitial lung disease. Despite extensive efforts in research during recent years, the mechanisms of the disease remain poorly understood. Evidence of an inflammatory mechanism, both supportive and contrary, is briefly reviewed in this paper. However, growing evidence has indicated that the apoptosis of alveolar epithelial cells (AECs) may be the early driving force of progression, with subsequent disrupted integrity of the alveolar-capillary basement membrane leading to an abnormal wound healing pathway. Thus, this paper will focus on outlining a process of pathogenesis of IPF from initial apoptosis of AECs to end lung remodeling.
Apoptosis
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Epithelial Cells
;
pathology
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Humans
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Idiopathic Pulmonary Fibrosis
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etiology
;
pathology
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Lung
;
pathology
9.Interaction of cancer-associated fibroblasts and tumor cells in carcinogenesis.
Journal of Zhejiang University. Medical sciences 2008;37(2):212-217
Tumor microenvironment is composed of mesenchymal cells and extracellular matrix components, which plays an important role in the growth, invasion and metastasis of tumor cells. Characteristic changes of stroma are usually accompanied with the malignant transformation of epithelial cells even ahead. The key component in the process-activated fibroblasts, also known as myofibroblasts, or cancer-associated fibroblasts (CAF), is the most abundant cells in tumor stroma. They promote the malignant transformation of epithelial cells through cell-cell communication via various soluble factors. This article reviews cancer-associated fibroblasts and their role in tumor development.
Cell Communication
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Cell Transformation, Neoplastic
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pathology
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Disease Progression
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Epithelial Cells
;
pathology
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Fibroblasts
;
pathology
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Humans
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Myoblasts
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pathology
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Neoplasms
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pathology
;
physiopathology
10.An experimental study on the apoptosis of rabbit small intestinal cells during early postburn stage.
Hong WANG ; Yu-lan MIAO ; Ke-xian MA ; Gang YAN ; Mao-xing GE ; He JIANG
Chinese Journal of Burns 2003;19(3):141-144
OBJECTIVETo explore the significance of apoptosis of rabbit small intestinal mucosal epithelial cells and lymphocytes, and lymphocytes of lumbrical process at early postburn stage.
METHODSTwenty-five Japanese white rabbits were randomly divided into 5 groups with 5 in each group, i.e. normal control (N), 3-postburn-hour group (3 PBH), 6 PBH, 12 PBH and 24 PBH groups. The rabbits in all PBH groups were inflicted with 30% TBSA III degree of flame burn on the back. The intestinal tissue samples were harvested from 5 anatomical sites for HE staining, electron microscopic examination and the detection of apoptosis in situ by TUNEL method at all the postburn time points. The results of TUNEL slides were analyzed statistically.
RESULTSHE staining revealed that there were relatively abundant apoptotic cells scattering solitarily in the lymph nodules and diffuse lymphatic tissue in the mucosal epithelial and mucosal lamina propria (and partially extended into the submucosal layer) of the intestine and lumbrical process in all burn groups. There were some disruption of intestinal mucosa in 24 PBH group. But no obvious inflammatory reaction and signs of necrosis were observed in all the slides. Apoptotic body formation could be identified by EM. Large number of blue-black positive cellular nuclei were revealed by TUNEL method with their distribution as similar to that found by HE staining. When comparing with those in control group, the apoptotic cells in small intestine and lumbrical process were increased obviously (P < 0.01) in 3 PBH group and reached the top level in 6 and 12 PBH groups (P < 0.01), declining thereafter to near value of 3 PBH in 24 PBH group, though it was still higher than control (P < 0.05). The number of apoptotic epithelial cells in middle distal portions of small intestinal mucosa in burn groups was much higher than that in proximal intestine (P < 0.05).
CONCLUSIONThere was a large number of apoptotic cells in rabbit small intestinal mucosal epithelium, gut associated lymphoid tissue and lymphocytes in the lumbrical process, especially in the middle and distal portions of the intestine. These change might be the cellular basis of postburn intestinal translocation of bacteria and endotoxin.
Animals ; Apoptosis ; Burns ; pathology ; Epithelial Cells ; pathology ; Female ; Intestinal Mucosa ; pathology ; Intestine, Small ; pathology ; Lymphocytes ; pathology ; Male ; Rabbits ; Time Factors