Comparison of Anti-Inflammatory Analgesics for Mechanical Stress-induced Inflammation in a Human Synovial Sarcoma Cell Line

Osteoarthritis is a complicated clinical condition affected by age, mechanical stress, cartilage hypertrophy, cytokines, and genetic predisposition. In this study, we compared the effects of various anti-inflammatory analgesics on mechanical stress-induced inflammation in a synovial sarcoma cell line （SW982 cells）. SW982 cells exposed to mechanical stress by shaking with hydroxyapatite-simulating bone chips were treated with acetaminophen, ketoprofen, triamcinolone acetonide, celecoxib, or neurotrophin for 48hr. The expression of integrin α5β1 receptor, observed in fibroblasts and synovium, was evaluated. Levels of the transcription factor, nuclear factor-κB, the inflammatory cytokine, tumor necrosis factor-α, the proteolytic enzyme, matrix metalloproteinase-3, and prostaglandin E2, which is associated with pain and arachidonate cascade product levels, were measured by ELISA. The expression of integrin α5β1 was significantly increased by mechanical stress. Activation of nuclear factor-κB by mechanical stress was significantly suppressed by celecoxib only. Mechanical stress-induced increases in tumor necrosis factor-α and matrix metalloproteinase-3 levels were significantly suppressed by acetaminophen, triamcinolone acetonide, and neurotrophin. The mechanical stress-induced increase in prostaglandin E2 levels was significantly suppressed by acetaminophen, ketoprofen, and celecoxib. SW982 exposed to mechanical stress is proposed as a model for arthritis, and indeed, the expression of integrin α5β1, a membrane receptor protein that binds to fibronectin and the extracellular matrix, and is involved in cell proliferation, differentiation, and neovascularization in osteoarthritis, was significantly upregulated. Following evaluation using this model, acetaminophen was found to possess anti-inflammatory, analgesic, and joint-destruction suppression properties. This drug may, therefore, have applications in the treatment of mechanical stress-induced inflammation

Relationship of Grade of Malignant Brain Tumor to Cancer Stem Cells and Survivin Expression

Glioblastoma (GBM) is difficult to completely cure by surgical treatment alone, and it is generally treated with a combination of surgery, radiotherapy, and chemotherapy. However, GBM is resistant to radiotherapy and chemotherapy, and complete cure cannot be achieved. Cancer stem cells (CSC) and survivin, which inhibit apoptosis, are considered as factors underlying tumor recurrence and the radiation- and drug-resistance of these tumors. We analyzed CSC and survivin expression in surgically excised specimens of malignant brain tumors to establish the relationships between the grades and CSC and survivin expression and between MIB-1 (Ki-67) expression and resistance. No relationship was noted between the grades and CSC or survivin expression, or between MIB-1 and CSC expression or between Grade 3 and 4 MIB-1 and survivin expression, although a correlation was noted between MIB-1 and survivin expression in Grade II tumors. These findings suggested that CSC are consistently contained in tumor tissue at a specific rate regardless of the histological grade, and the apoptosis of cells with low-level proliferative and cell cycling activities does not occur because these cells do not respond to chemotherapy or radiation, being resistant to treatment

Eribulin Treatment Induces High Expression of miR-195 and Inactivates the Wnt/β - catenin Signaling Pathway in Triple-negative Breast Cancer

Triple-negative breast cancer （TNBC） accounts for 10-15％ of all breast cancer cases and shows a poor prognosis with 30％ distant metastasis. With few specific target molecules and ineffective hormonal and anti-HER2 treatment, an alternative therapeutic method for TNBC is urgently required. Recently, a non-taxane inhibitor of microtubule dynamics called eribulin was developed for breast cancer therapy. Eribulin induces irreversible mitotic mass formation in cancer cells during the G2-M phase, initiating apoptosis; however, the mechanism underlying this eribulin activity remains unclear. We reported previously that exposing non-basal-like （NBL） TNBC cells to eribulin increases miR-195 expression, which in turn decreases the expression of targeted Wnt3a. The present study sought to further clarify the mechanism of this antitumor effect by exploring how eribulin affects Wnt/β - catenin signaling based on miRNA expression changes in TNBC. In an NBL type of human breast cancer cell line （MDA-MB-231 cells）, we compared the expression levels of Wnt/β catenin signaling pathway proteins in cells exposed to an miR-195 mimic （cells transfected with miR-195 and in which Wnt3a expression was suppressed） and in cells exposed to eribulin. Expression levels of Wnt3a, β -catenin, and GSK-3β were measured by ELISA and observed by fluorescence immunostaining. Wnt3a and β -catenin expression was significantly lower and GSK-3β expression was significantly higher in the cells exposed to eribulin and transfected with miR-195 mimic than in the untreated controls, suggesting that eribulin inactivates the Wnt/β -catenin signaling pathway. Therefore, a novel antitumor mechanism of eribulin was determined, whereby eribulin induces high expression of miR-195 to inactivate the Wnt/β -catenin signaling pathway in NBL-type TNBC

Quantification of (–)-Epigallocatechin-3-gallate Inhibition of Anaplastic Thyroid Cancer Cell Line Adhesion and Proliferation Using Real-time Cell Analysis

Anaplastic thyroid cancer (ATC) has a poor prognosis because of immediate metastasis. Several studies in humans and animals have suggested that the ingestion of green tea or its active ingredient (–)-epigallocatechin-3-gallate (EGCG) may decrease the risk of cancer. Using a recently developed real-time cell analysis (RTCA) system, we have shown previously that EGCG inhibits cell migration and the invasion of oral cavity cancers by suppressing matrix metalloproteinases. In the present study we used RTCA to investigate the effects of EGCG on cell adhesion to fibronectin-coated plates using three cancer cell lines: one ATC cell line (TCO-1) and two poorly differentiated oral squamous cell carcinomas (OSCCs) cell lines (SAS and HO-1-u-1; originating from the tongue and floor of the mouth, respectively). EGCG (50µM) inhibited the adhesion of all three cell lines. In addition to its effects on cell adhesion, 50µM EGCG inhibited the cell proliferation of TCO-1 cells. Furthermore, EGCG decreased αV integrin (ITGAV) mRNA levels in all three cell lines, suggesting that EGCG inhibits the cell adhesion and proliferation of OSCC and ATC cells via suppression of integrin expression. Therefore, EGCG represents a useful dietary constituent or a lead compound for counteracting metastasis of oral cavity cancers and thyroid cancers

Apoptosis-induced Proliferation in UV-Irradiated Human Conjunctival Epithelial Cells

A pterygium is a benign growth that develops on the conjunctiva and, in some cases, extends to the cornea and interferes with vision. Excessive exposure to ultraviolet (UV) light is one of the causes of pterygium development. We previously reported that UV-induced apoptosis is led by production of reactive oxygen species (ROS) that activate p38 mitogen-activated protein kinase (MAPK) in human conjunctival epithelial (HCE) cells. Also, ROS-dependent induction of interleukin-11 (IL-11) has been reported to upregulate MAPK pathways, which results in compensatory proliferation. In this study, we examined the effect of UV exposure on HCE cells, in terms of change in apoptosis, ROS generation, phosphorylation of c-Jun N-terminal kinase (JNK), levels of IL-11 (a key cytokine in tissue repair and compensatory proliferation), production of activator protein 1 (AP-1), and expression of c-myc, c-fos and c-jun (which provides evidence of healthy cell proliferation). Apoptosis in HCE cells was induced by UV light irradiation (312nm, 4.94mW/cm2). Apoptosis was measured using the Muse Annexin V and Dead Cell Assay Kit. ROS generation was measured by using 5-(and 6-) chloromethyl-2\u277\u27-dichlorodihydrofluorescein diacetate, acetyl ester. JNK phosphorylation, IL-11 levels and AP-1 production were measured by enzyme-linked immunosorbent assays (ELISAs). Imnunocytochemical staining was used to measure c-myc, c-fos and c-jun expression. UV irradiation increased ROS generation, phosphorylation of JNK, and apoptotic cell count. IL-11 levels and AP-1 production were significantly increased by UV irradiation. The irradiated cells had increased expression of c-myc, c-fos and c-jun, and treatment of the cells with IL-11 significantly increased expression of c-myc, c-fos and c-jun. These results suggest that the release of IL-11 from UV-induced apoptotic HCE cells and surrounding healthy cells could promote proliferation to maintain homeostasis

ヒフ ランダム セイケン ガ シンダン ニ ユウヨウ デ アッタ ケッカンナイ リンパシュ ノ イチレイ

A６２‐year‐old woman was referred to our hospital for further examination of fever of unknown origin, splenomegaly and pancytopenia. On admission, she had persistent fever and psychological symptoms. Blood examination showed pancytopenia and elevated level of LDH, soluble IL‐２receptor and ferritin. Computed tomography showed multiple low density areas in the spleen, but no systemic lymphadenopathy. In magnetic resonance imaging of the pons, a low and high intensity area on T１‐and T２‐weighted image, respectively, was detected. Taken together these findings, she was suspected to have hepatosplentic T-cell lymphoma or intravascular large B-cell lymphoma. To make a definite diagnosis, random skin biopsy was performed. Immunohistochemical stainings revealed the massive infiltration of CD２０‐and CD７９α‐positive large lymphoid cells inside the vessels, which yielded the diagnosis of intravascular large B-cell lymphoma

Analysis of miRNA Expression in Breast Cancer

Triple-negative breast cancer (TNBC), lacking estrogen receptor (ER), progesterone receptor (PgR), and human epidermal growth factor receptor (HER2) expression, is resistant to conventional therapies. Recent studies have focused on microRNAs (miRNAs) as novel molecular targets for treating TNBC because they modulate gene expression and tumor progression. In the current study, we analyzed the expression of selected miRNAs (miR-145 and miR-182) and tumor promoting factors such as Fascin and poly (ADP-ribose) polymerase (PARP) in human TNBC tissues and "Luminal A" breast cancer tissues, which express ER and PgR, but not HER2, as well as breast cancer cell lines including the triple-negative MDA-MB-231 and Luminal A MCF-7. The results showed that miR-145 and miR-182 were expressed in Luminal A breast cancer tissues and MCF-7 cells, but not in TNBC tissues and MDA-MB-231 cells. In contrast, Fascin and PARP proteins were highly expressed in TNBC and MDA-MB-231, but poorly expressed in Luminal A tissues and MCF-7 cells, indicating a negative correlation between expression of these miRNAs and that of the tumor promoting factors Fascin and PARP. The current study therefore suggests that miR-145 and miR-182 could be potential novel therapeutic targets for TNBC therapy

Suppressive Effects of Catechins in UV-Induced Cytotoxicity of Human Corneal Epithelial Cells

Photokeratitis is a disease in which the ocular surface is directly affected by oxidative stress caused by exposure to ultraviolet （UV） light and oxygen. It is speculated that the production of free radicals and reactive oxygen species （ROS） is caused by UV-induced cytotoxicity. Recent studies have reported that catechins have antioxidant, antiallergic, antitumor, and antibacterial effects. The aim of our study was to investigate the mechanism of UV-induced cytotoxicity in cultured human corneal epithelial （HCE-T） cells and evaluate the protective effects of the catechins, （?）-epigallocatechin gallate （EGCG） and （?）-epigallocatechin 3-O-（3-O-methyl） gallate （EGCG3”Me）, on apoptosis. HCE-T cells were UV irradiated at 312nm （4.94mW/cm2, 296mJ/cm2）. EGCG and EGCG3”Me were dissolved in methanol and adjusted to 5, 10, or 20?M. Absorption was measured from 250 to 400nm. EGCG and EGCG3”Me were pre-incubated for 1 hr. After UV irradiation, membrane lipid peroxide, tumor necrosis factor （TNF）-α production, ROS generation, caspase-3 and -8 activities, mitochondrial membrane potential, and cytochrome c levels were measured. Both EGCG and EGCG3”Me had UV absorption, and increased with concentration dependently. The increases in the levels of membrane lipid hyperoxidation, activation of caspase-3 and -8, production of TNF-α and ROS were found, by UV irradiation, to be significant. But these levels were significantly decreased by pretreatment with EGCG and EGCG3”Me. There were no changes in mitochondrial membrane potential and cytoplasmic cytochrome c levels after UV irradiation. Oxidative stress occurs early near the cell membrane in response to UV irradiation. As a result, TNF-α is induced, leading to apoptosis mainly through caspase-8 activation. Conversely, EGCG and EGCG3”Me absorb UV light directly and inhibit lipid peroxidation in the cell membrane. Catechins inhibit the apoptosis cascade by inactivating caspase-3 and caspase-8

Cancer stem-like cells have cisplatin resistance and miR-93 regulate p21 expression in breast cancer

Aim: This study aims to examine the role of microRNAs (miRNAs) in regulating the expression of p21, a cyclin-dependent kinase inhibitor, and in inducing resistance to cisplatin, an anticancer drug. Methods: Human breast cancer cell line MDA-MB231 cells were separated into two subpopulations, cancer stem-like cells (CSCs) and cancer cells, based on the expression of cell surface antigens CD44 and CD24. Results: p21 protein expression was higher in CSCs than in cancer cells. Exposure of MDA-MB-231 cells to cisplatin increased p21 protein expression. However, p21 expression was significantly lower in cisplatin-treated CSCs than in cisplatin-treated cancer cells, suggesting that p21-dependent cell cycle suppression was lower in CSCs than in cancer cells. Moreover, caspase-3 activity was significantly lower in cisplatin-treated CSCs than in cisplatin-treated cancer cells, indicating that CSCs were more resistant to cisplatin-induced apoptosis than cancer cells. Treatment with miR-93 inhibitors increased p21 expression in CSCs, suggesting that miR-93 suppressed p21 expression. Conclusion: The results of the present study indicate that CSCs contribute to cisplatin resistance of MDA-MB231 cells and suggest that miR-93 inhibits the expression of p21, a factor involved in drug resistance

Establishment of a Mechanical Stress Load Arthritis Model in a Human Synovial Sarcoma Cell Line

Osteoarthritis （OA） is a degenerative disease that occurs in joints throughout the body and includes various concomitant pathologies due to possible mechanical stress, such as destruction of cartilage, hyperplasic changes, and synovial inflammation. However, there have been few studies on the mechanical stress that is the basic cause of OA. Our goal was to establish an OA model at the cellular level, by measuring inflammatory cytokines and cartilage destruction markers that are induced after a mechanical stress load. Using a human synovial sarcoma cell line （SW982 cells）, we provided two types of mechanical stress load for 48hr: shaking stress （amplitude 2mm, speed range 1,000rpm）, and the addition of hydroxyapatite （5?g/ml） into the culture medium. Then we measured the phosphorylation activity of nuclear factor （NF）-κB transcription factor in the cell lysate, and the levels of tumor necrosis factor （TNF）-α and interleukin （IL）-6 as inflammatory cytokines, and the level of matrix metalloproteinase （MMP）-3 as a cartilage destruction marker, released in the medium. Shaking stress significantly induced phosphorylation of NF-κB and production of TNF-α, compared with untreated controls. On the other hand, hydroxyapatite stress only increased production of TNF-α. Both stresses together significantly induced phosphorylation of NF-κB and production of TNF-α, IL-6 and MMP-3 rather than a single stress load. In this study, markers related to inflammation and cartilage destruction （IL-6, TNF-α, and MMP-3） significantly increased. Therefore, we suggest that the mechanical stress load conditions used in this study might be useful as an OA model