keyword
https://read.qxmd.com/read/32065351/arctigenin-induces-necroptosis-through-mitochondrial-dysfunction-with-ccn1-upregulation-in-prostate-cancer-cells-under-lactic-acidosis
#21
JOURNAL ARTICLE
Yoon-Jin Lee, Hae-Seon Nam, Moon-Kyun Cho, Sang-Han Lee
Arctigenin, a mitochondrial complex I inhibitor, has been identified as a potential anti-tumor agent, but the involved mechanism still remains elusive. Herein, we studied the underlying mechanism(s) of action of arctigenin on acidity-tolerant prostate cancer PC-3AcT cells in the lactic acid-containing medium. At concentration showing no toxicity on normal prostate epithelial RWPE-1 and HPrEC cells, arctigenin alone or in combination with docetaxel induced significant cytotoxicity in PC-3AcT cells compared to parental PC-3 cells...
February 17, 2020: Molecular and Cellular Biochemistry
https://read.qxmd.com/read/31957543/zika-virus-promotes-ccn1-expression-via-the-camkii%C3%AE-creb-pathway-in-astrocytes
#22
JOURNAL ARTICLE
Jianhong Sun, Wanpo Zhang, Zhongyuan Tan, Caishang Zheng, Yan Tang, Xianliang Ke, Yuan Zhang, Yan Liu, Penghui Li, Qinxue Hu, Hanzhong Wang, Panyong Mao, Zhenhua Zheng
Zika virus (ZIKV) infection in the human central nervous system (CNS) causes Guillain-Barre syndrome, cerebellum deformity, and other diseases. Astrocytes are immune response cells in the CNS and an important component of the blood-brain barrier. Consequently, any damage to astrocytes facilitates the spread of ZIKV in the CNS. Connective tissue growth factor/Nephroblastoma overexpressed gene family 1 (CCN1), an important inflammatory factor secreted by astrocytes, is reported to regulate innate immunity and viral infection...
December 2020: Virulence
https://read.qxmd.com/read/31769620/ccn1-stimulated-the-osteoblasts-via-pten-akt-gsk3%C3%AE-cyclind1-signal-pathway-in-myeloma-bone-disease
#23
JOURNAL ARTICLE
Siyang Yan, Hui Liu, Zhaoyun Liu, Fengping Peng, Fengjuan Jiang, Lijuan Li, Rong Fu
BACKGROUNDS: Myeloma-related bone disease (MBD) is a common complication of multiple myeloma (MM), which can both decrease life quality and influence the prognosis of the patients. We have found that CCN1 stimulated proliferation and differentiation of osteoblasts in MM in vitro and in vivo, while its mechanism still remains unknown. METHOD: Bone marrow mononuclear cells were collected from MM patients and differentiated into the osteoblasts. After co-culture with CCN1 in vitro, the intracellular signaling antibody array and western blot were performed to explore the signaling pathway...
January 2020: Cancer Medicine
https://read.qxmd.com/read/31731760/ccn2-mediates-s1p-induced-upregulation-of-cox2-expression-in-human-granulosa-lutein-cells
#24
JOURNAL ARTICLE
Liao-Liao Hu, Hsun-Ming Chang, Yuyin Yi, Yingtao Liu, Elizabeth L Taylor, Li-Ping Zheng, Peter C K Leung
CCN1 and CCN2 are members of the CCN family and play essential roles in the regulation of multiple female reproductive functions, including ovulation. Cyclooxygenase-2 (COX2) is a critical mediator of ovulation and can be induced by sphingosine-1-phosphate (S1P) through the S1P1/3 -mediated Yes-associated protein (YAP) signaling. However, it is unclear whether CCN1 or CCN2 can mediate S1P-induced upregulation of COX2 expression and increase in prostaglandin E2 (PGE2) production in human granulosa-lutein (hGL) cells...
November 15, 2019: Cells
https://read.qxmd.com/read/31233838/cell-intrinsic-pd-1-promotes-proliferation-in-pancreatic-cancer-by-targeting-cyr61-ctgf-via-the-hippo-pathway
#25
JOURNAL ARTICLE
Ning Pu, Shanshan Gao, Hanlin Yin, Jian-Ang Li, Wenchuan Wu, Yuan Fang, Lei Zhang, Yefei Rong, Xuefeng Xu, Dansong Wang, Tiantao Kuang, Dayong Jin, Jun Yu, Wenhui Lou
Pancreatic ductal adenocarcinoma (PDAC) remains a refractory disease. Programmed cell death protein-1 (PD-1) monotherapy has shown strong performance in targeting several malignancies. However, the effect and mechanism of intrinsic PD-1 in pancreatic cancer cells is still unknown. In this study, associations between clinicopathological characteristics and stained tissue microarrays of PDAC specimens were analyzed along with profiling and functional analyses. The results showed that cell-intrinsic PD-1 was significantly correlated with overall survival (OS)...
September 28, 2019: Cancer Letters
https://read.qxmd.com/read/31170244/yin-yang-expression-of-ccn-family-members-transforming-growth-factor-beta-1-via-alk5-fak-mek-induces-ccn1-and-ccn2-yet-suppresses-ccn3-expression-in-human-dermal-fibroblasts
#26
JOURNAL ARTICLE
Alexander Peidl, Bernard Perbal, Andrew Leask
The role of the microenvironment in driving connective tissue disease is being increasingly appreciated. Matricellular proteins of the CCN family are signaling modifiers that are secreted by cells into the extracellular matrix microenvironment where they have profound, context-dependent effects on organ development, homeostasis and disease. Indeed, CCN proteins are emergent targets for therapeutic intervention. Recent evidence suggests that, in vivo, CCN3 has effects opposing CCN2. Moreover, when CCN3 expression is high, CCN2 expression is low...
2019: PloS One
https://read.qxmd.com/read/30465121/molecular-signatures-for-ccn1-p21-and-p27-in-progressive-mantle-cell-lymphoma
#27
JOURNAL ARTICLE
Afak Rasheed Salman Zaidi, Sadie Dresman, Charlotte Burt, Simon Rule, Lynn McCallum
Mantle cell lymphoma (MCL) is a comparatively rare non-Hodgkin's lymphoma characterised by overexpression of cyclin D1. Many patients present with or progress to advanced stage disease within 3 years. MCL is considered an incurable disease with median survival between 3 and 4 years. We have investigated the role(s) of CCN1 (CYR61) and cell cycle regulators in progressive MCL. We have used the human MCL cell lines REC1 < G519 < JVM2 as a model for disease aggression. The magnitude of CCN1 expression in human MCL cells is REC1 > G519 > JVM2 cells by RQ-PCR, depicting a decrease in CCN1 expression with disease progression...
September 2019: Journal of Cell Communication and Signaling
https://read.qxmd.com/read/30121256/dna-methylation-reduces-the-yes-associated-protein-1-ww-domain-containing-transcription-regulator-1-pathway-and-prevents-pathologic-remodeling-during-bladder-obstruction-by-limiting-expression-of-bdnf
#28
JOURNAL ARTICLE
Martin Sidler, Karen J Aitken, Jia-Xin Jiang, Chris Sotiropoulos, Prateek Aggarwal, Arsalan Anees, Cynthia Chong, Aliza Siebenaller, Thenuka Thanabalasingam, J Maxwell White, Sanaa Choufani, Rosanna Weksberg, Bruno Sangiorgi, Jeff Wrana, Paul Delgado-Olguin, Darius J Bägli
Chronic bladder obstruction and bladder smooth muscle cell (SMC) stretch provide fibrotic and mechanical environments that can lead to epigenetic change. Therefore, we examined the role of DNA methylation in bladder pathology and transcriptional control. Sprague-Dawley female rats underwent partial bladder obstruction by ligation of a silk suture around the proximal urethra next to a 0.9-mm steel rod. Sham operation comprised passing the suture around the urethra. After 2 weeks, rats were randomized to normal saline or DNA methyltransferase inhibitor, 5-aza-2-deoxycytidine (DAC) at 1 mg/kg, three times/week intraperitoneally...
October 2018: American Journal of Pathology
https://read.qxmd.com/read/30044965/portal-myofibroblasts-are-sensitive-to-ccn-mediated-endoplasmic-reticulum-stress-related-apoptosis-with-potential-to-attenuate-biliary-fibrogenesis
#29
JOURNAL ARTICLE
Erawan Borkham-Kamphorst, Bettina Therese Steffen, Eddy van de Leur, Ute Haas, Ralf Weiskirchen
Portal fibroblasts are mesenchyme-derived fibroblasts surrounding the bile ducts, and activated into portal myofibroblasts (pMF) during cholestatic liver injury. pMF express α-smooth muscle actin (α-SMA) and produce the fibrogenic extracellular matrix (ECM) collagen type I and fibronectin, playing important roles in portal fibrosis. A cholestatic bile duct-ligated (BDL) model is characterized by impaired hepatobiliary excretion of bile, leading to increased bile acid accumulation. Accumulation of bile acids is known to induce endoplasmic reticulum (ER) stress leading to liver damage and cell death...
November 2018: Cellular Signalling
https://read.qxmd.com/read/28039333/involvement-of-hypoxia-inducing-factor-1%C3%AE-dependent-plasminogen-activator-inhibitor-1-up-regulation-in-cyr61-ccn1-induced-gastric-cancer-cell-invasion
#30
JOURNAL ARTICLE
Ming-Tsan Lin, I-Hsin Kuo, Cheng-Chi Chang, Chia-Yu Chu, Hsing-Yu Chen, Been-Ren Lin, Munisamy Sureshbabu, Hou-Jung Shih, Min-Liang Kuo
No abstract text is available yet for this article.
December 30, 2016: Journal of Biological Chemistry
https://read.qxmd.com/read/26697179/ccn1-suppresses-pulmonary-vascular-smooth-muscle-contraction-in-response-to-hypoxia
#31
JOURNAL ARTICLE
Seon-Jin Lee, Meng Zhang, Kebin Hu, Ling Lin, Duo Zhang, Yang Jin
Pulmonary vasoconstriction and increased vascular resistance are common features in pulmonary hypertension (PH). One of the contributing factors in the development of pulmonary vasoconstriction is increased pulmonary artery smooth muscle cell (PASMC) contraction. Here we report that CCN1, an extracellular matrix molecule, suppressed PASMC contraction in response to hypoxia. CCN1 (Cyr61), discovered in past decade, belongs to the Cyr61-CTGF-Nov (CCN) family. It carries a variety of cellular functions, including angiogenesis and cell adhesion, death, and proliferation...
December 2015: Pulmonary Circulation
https://read.qxmd.com/read/26459773/ccn1-cyr61-pi3k-akt-signaling-promotes-retinal-neovascularization-in-oxygen-induced-retinopathy
#32
JOURNAL ARTICLE
Yu Di, Yiou Zhang, Qingzhu Nie, Xiaolong Chen
Retinal neovascularization (RNV) is a characteristic pathological finding of retinopathy of prematurity (ROP). Cysteine-rich 61 [Cyr61, also known as CCN family member 1 (CCN1)] has been reported to mediate angiogenesis. The aim of the present study was to investigate the mechanisms of CCN1/Cyr61-phosphoinositide 3-kinase (PI3K)/AKT signaling in ROP. The contribution of CCN1 to human umbilical vein endothelial cell (HUVEC) proliferation and apoptosis under hypoxic conditions was determined using a cell counting kit‑8 (CCK-8) and Annexin V/propidium iodide (PI) staining, respectively, as well as using siRNA targeting CCN1 (CCN1 siRNA)...
December 2015: International Journal of Molecular Medicine
https://read.qxmd.com/read/26393424/ccn1-acutely-increases-nitric-oxide-production-via-integrin-%C3%AE-v%C3%AE-3-akt-s6k-phosphorylation-of-endothelial-nitric-oxide-synthase-at-the-serine-1177-signaling-axis
#33
JOURNAL ARTICLE
Soojin Hwang, Hyeon-Ju Lee, Gyungah Kim, Kyung-Jong Won, Yoon Shin Park, Inho Jo
Although CCN1 (also known as cysteine-rich, angiogenic inducer 61, CYR61) has been reported to promote angiogenesis and neovascularization in endothelial cells (ECs), its effects on endothelial nitric oxide (NO) production have never been studied. Using human umbilical vein ECs, we investigated whether and how CCN1 regulates NO production. CCN1 acutely increased NO production in a time- and dose-dependent manner, which was accompanied by increased phosphorylation of endothelial NO synthase (eNOS) at serine 1177 (eNOS-Ser(1177)), but not that of eNOS-Thr(495) or eNOS-Ser(114)...
December 2015: Free Radical Biology & Medicine
https://read.qxmd.com/read/26281901/cell-based-assay-system-for-high-throughput-screening-of-anti-photo-aging-agents-in-fibroblast-transfectants
#34
JOURNAL ARTICLE
S Lee, S Shin, E Jung, D Park
The matricellular protein CCN1 is significantly elevated in acutely ultraviolet-irradiated human skin and negatively regulates collagen homeostasis by suppressing collagen synthesis and increasing collagen degradation. In this study, we established a stable cell line, termed CCN1-GFs, by transfection of the pAcGFP1-1-CCN1 promoter plasmid and examined its usefulness as a cell-based assay system for screening anti-aging ingredients. The promoter of the reporter plasmid pAcGFP1-1-CCN1 promoter was transfected into NIH3T3 cells using the Lipofectamine reagent...
August 2016: Cytotechnology
https://read.qxmd.com/read/26028023/the-matricellular-protein-ccn1-suppresses-hepatocarcinogenesis-by-inhibiting-compensatory-proliferation
#35
JOURNAL ARTICLE
C-C Chen, K-H Kim, L F Lau
Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related deaths worldwide, and is on the rise in the United States. Previous studies showed that the matricellular protein CCN1 (CYR61) is induced during hepatic injuries and functions to restrict and resolve liver fibrosis. Here, we show that CCN1 suppresses hepatocarcinogenesis by inhibiting carcinogen-induced compensatory hepatocyte proliferation, thus limiting the expansion of damaged and potentially oncogenic hepatocytes. Consistent with tumor suppression, CCN1 expression is downregulated in human HCC...
March 10, 2016: Oncogene
https://read.qxmd.com/read/25822023/ccn1-induces-hepatic-ductular-reaction-through-integrin-%C3%AE-v%C3%AE-%C3%A2-mediated-activation-of-nf-%C3%AE%C2%BAb
#36
JOURNAL ARTICLE
Ki-Hyun Kim, Chih-Chiun Chen, Gianfranco Alpini, Lester F Lau
Liver cholestatic diseases, which stem from diverse etiologies, result in liver toxicity and fibrosis and may progress to cirrhosis and liver failure. We show that CCN1 (also known as CYR61), a matricellular protein that dampens and resolves liver fibrosis, also mediates cholangiocyte proliferation and ductular reaction, which are repair responses to cholestatic injury. In cholangiocytes, CCN1 activated NF-κB through integrin αvβ5/αvβ3, leading to Jag1 expression, JAG1/NOTCH signaling, and cholangiocyte proliferation...
May 2015: Journal of Clinical Investigation
https://read.qxmd.com/read/25187949/ccn1-induces-oncostatin-m-production-in-osteoblasts-via-integrin-dependent-signal-pathways
#37
JOURNAL ARTICLE
Cheng-Yu Chen, Chen-Ming Su, Yuan-Li Huang, Chun-Hao Tsai, Lih-Jyh Fuh, Chih-Hsin Tang
Inflammatory response and articular destruction are common symptoms of osteoarthritis. Cysteine-rich 61 (CCN1 or Cyr61), a secreted protein from the CCN family, is associated with the extracellular matrix involved in many cellular activities like growth and differentiation. Yet the mechanism of CCN1 interacting with arthritic inflammatory response is unclear. This study finds CCN1 increasing expression of oncostatin m (OSM) in human osteoblastic cells. Pretreatment of αvβ3 monoclonal antibody and inhibitors of focal adhesion kinase (FAK), c-Src, phosphatidylinositol 3-kinase (PI3K), and NF-κB inhibited CCN1-induced OSM expression in osteoblastic cells...
2014: PloS One
https://read.qxmd.com/read/25106095/induction-of-the-matricellular-protein-ccn1-through-rhoa-and-mrtf-a-contributes-to-ischemic-cardioprotection
#38
JOURNAL ARTICLE
Xia Zhao, Eric Y Ding, Olivia M Yu, Sunny Y Xiang, Valerie P Tan-Sah, Bryan S Yung, Joe Hedgpeth, Richard R Neubig, Lester F Lau, Joan Heller Brown, Shigeki Miyamoto
Activation of RhoA, a low molecular-weight G-protein, plays an important role in protecting the heart against ischemic stress. Studies using non-cardiac cells demonstrate that the expression and subsequent secretion of the matricellular protein CCN1 is induced by GPCR agonists that activate RhoA. In this study we determined whether and how CCN1 is induced by GPCR agonists in cardiomyocytes and examined the role of CCN1 in ischemic cardioprotection in cardiomyocytes and the isolated perfused heart. In neonatal rat ventricular myocytes (NRVMs), sphingosine 1-phosphate (S1P), lysophosphatidic acid (LPA) and endothelin-1 induced robust increases in CCN1 expression while phenylephrine, isoproterenol and carbachol had little or no effect...
October 2014: Journal of Molecular and Cellular Cardiology
https://read.qxmd.com/read/24631528/ccn1-enables-fas-ligand-induced-apoptosis-in-cardiomyoblast-h9c2-cells-by-disrupting-caspase-inhibitor-xiap
#39
JOURNAL ARTICLE
Bor-Chyuan Su, Fan-E Mo
Cell proliferation from pre-existing cardiomyocytes is a major source of cells for normal mammalian myocardial renewal or for regeneration after myocardial injury. These proliferative cardiomyocytes may act differently from the postmitotic cardiomyocytes in a stressed heart. Extracellular matrix molecule CCN1 is produced to promote Fas ligand (FasL)-induced cardiomyocyte apoptosis in mice with stress-induced cardiac injury. We aimed to investigate the effect of CCN1 on the proliferative cardiomyocytes. We used rat embryonic cardiomyoblast H9c2 cells to study the cardiotoxicity of CCN1...
June 2014: Cellular Signalling
https://read.qxmd.com/read/24567145/alk5-inhibition-blocks-tgf%C3%AE-induced-ccn1-expression-in-human-foreskin-fibroblasts
#40
JOURNAL ARTICLE
Katherine Thompson, Hannah Murphy-Marshman, Andrew Leask
The potent profibrotic cytokine TGFβ induces connective tissue growth factor (CCN2/CTGF) is induced in fibroblasts in a fashion sensitive to SB-431542, a specific pharmacological inhibitor of TGFβ type I receptor (ALK5). In several cell types, TGFβ induces CCN1 but suppresses CCN3, which opposes CCN1/CCN2 activities. However, whether SB-431542 alters TGFβ-induced CCN1 or CCN3 in human foreskin fibroblasts in unclear. Here we show that TGFβ induces CCN1 but suppresses CCN3 expression in human foreskin fibroblasts in a SB-431542-sensitive fashion...
March 2014: Journal of Cell Communication and Signaling
keyword
keyword
165869
2
3
Fetch more papers »
Fetching more papers... Fetching...
Remove bar
Read by QxMD icon Read
×

Save your favorite articles in one place with a free QxMD account.

×

Search Tips

Use Boolean operators: AND/OR

diabetic AND foot
diabetes OR diabetic

Exclude a word using the 'minus' sign

Virchow -triad

Use Parentheses

water AND (cup OR glass)

Add an asterisk (*) at end of a word to include word stems

Neuro* will search for Neurology, Neuroscientist, Neurological, and so on

Use quotes to search for an exact phrase

"primary prevention of cancer"
(heart or cardiac or cardio*) AND arrest -"American Heart Association"

We want to hear from doctors like you!

Take a second to answer a survey question.