نتایج جستجو برای: پروتیین grp78

تعداد نتایج: 2989  

Journal: :Cancer research 1995
S Chatterjee M F Cheng R B Berger S J Berger N A Berger

We have recently demonstrated that cell lines deficient in poly(ADP-ribose) synthesis due to deficiency in the enzyme poly(ADP-ribose) polymerase (PADPRP) or depletion of its substrate NAD+ overexpress GRP78. Furthermore, this overexpression of GRP78 is associated with the acquisition of resistance to topoisomerase II-directed drugs such as etoposide (VP-16); (S. Chatterjee et al., Cancer Res.,...

2017
Hyo-Jin Park Jae-Young Park Jin-Woo Kim Seul-Gi Yang Jae-Min Jung Min-Ji Kim Joung Jun Park Deog-Bon Koo

In the present study, we investigated the role of binding immunoglobulin protein/glucose-regulated protein, 78-kDa (BIP/GRP78)-regulated endoplasmic reticulum (ER)-stress on meiotic maturation and cumulus cells expansion in porcine cumulus-oocyte complexes (COCs). Previously, it has been demonstrated that unfolded protein response (UPR)-related genes, such as molecules involved in ER-stress def...

Journal: :Cancer research 2006
Eunjung Lee Peter Nichols Darcy Spicer Susan Groshen Mimi C Yu Amy S Lee

The discovery of predictive factors for chemoresistance is critical for improving adjuvant therapy for cancer patients. The 78-kDa glucose-regulated protein (GRP78), widely used as an indicator of the unfolded protein response (UPR), is induced in the tumor microenvironment. In vitro studies suggest that GRP78 confers chemoresistance to topoisomerase inhibitors, such as Adriamycin (doxorubicin)...

2016
Mina Thon Toru Hosoi Koichiro Ozawa

Leptin, an adipocyte-derived hormone, centrally regulates energy homeostasis. Overlaps in the regulation of glucose and energy homeostasis have been reported between leptin and insulin. However, the effects of insulin on leptin's actions in the central nervous system (CNS) have not yet been elucidated in detail. In the present study, we found that insulin potentiated leptin's actions through GR...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2006
Llana Pootrakul Ram H Datar Shan-Rong Shi Jie Cai Debra Hawes Susan G Groshen Amy S Lee Richard J Cote

BACKGROUND Induction of molecular chaperone Grp78 (78-kDa glucose-regulated protein) occurs in stress conditions that often characterize tumor microenvironments. We investigated the role of Grp78 in prostate cancer progression and the development of castration resistance, where cancer cells continue to survive despite the stress of an androgen-starved environment. EXPERIMENTAL DESIGN Immunohi...

2017
David R. Soto-Pantoja Adam S. Wilson Kenysha YJ. Clear Brian Westwood Pierre L. Triozzi Katherine L. Cook

The unfolded protein response (UPR) is a stress pathway controlled by GRP78 to mediate IRE1, PERK, and ATF6 signaling. We show that targeting GRP78, IRE1, and PERK differentially regulates macrophage polarization. Specifically, PERK targeting enhanced macrophage proliferation and macrophage-mediated killing but not GRP78 or IRE1. Targeting UPR in cancer cells also differentially affected macrop...

2014
Mina Thon Toru Hosoi Michiko Yoshii Koichiro Ozawa

Leptin is a circulating hormone that plays a critical role in regulating energy expenditure and food intake. Evidence to suggest the involvement of endoplasmic reticulum (ER) stress in the development of obesity is increasing. To adapt against ER stress, cells trigger the unfolded protein response (UPR). The 78 kDa glucose-regulated protein (GRP78) is an ER chaperone that protects cells against...

2014
Xiuna Jing Qiaoyun Shi Wei Bi Zhifen Zeng Yanran Liang Xia Wu Songhua Xiao Jun Liu Lianhong Yang Enxiang Tao

Rifampicin has been proposed as a therapeutic candidate for Parkinson's disease (PD). We previously showed that rifampicin was neuroprotective in PD models in vivo and in vitro. However, the molecular mechanisms underlying are not fully elucidated. In this study, using the comprehensive proteomic analysis, we identified that the 78 kDa glucose-regulated protein (GRP78), a hallmark of the unfold...

2012
Seung-Ah Yoo Sungyong You Hyung-Ju Yoon Dong-Ho Kim Hyun-Sook Kim Kyungho Lee Jin Hee Ahn Daehee Hwang Amy S. Lee Ki-Jo Kim Yune-Jung Park Chul-Soo Cho Wan-Uk Kim

An accumulation of misfolded proteins can trigger a cellular survival response in the endoplasmic reticulum (ER). In this study, we found that ER stress-associated gene signatures were highly expressed in rheumatoid arthritis (RA) synoviums and synovial cells. Proinflammatory cytokines, such as TNF and IL-1β, increased the expression of GRP78/BiP, a representative ER chaperone, in RA synoviocyt...

Journal: :Biological & pharmaceutical bulletin 2014
Kazushi Matsumura Chika Sakai Shigeru Kawakami Fumiyoshi Yamashita Mitsuru Hashida

Proteasome inhibitors are a novel class of molecular-targeted anti-cancer drugs that suppress the degradation of malfolded proteins, trigger endoplasmic reticulum (ER) stress, and activate apoptosis signals. Glucose-regulated protein 78 (GRP78), a major ER chaperone, is one of the most important molecules for transduction of unfolded protein response (UPR) signals. In accordance with past findi...

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