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Article ; Online: GABA

Wei, Bo / Zhu, Yini / Yang, Peng / Han, Yong / Wang, Suyun / Wang, Xiaomei / Xia, Shuai / Song, Xiaoguang / Zhang, Zhongling / Wang, Sheng / Rondard, Philippe / Pin, Jean-Philippe / Jiang, Xinnong / Liu, Jianfeng

iScience

2021 Volume 24, Issue 11, Page(s) 103311

Abstract: Neurotransmitter receptors are involved in cancer progression. Among them, the heterodimeric ... ...

Abstract	Neurotransmitter receptors are involved in cancer progression. Among them, the heterodimeric GABA
Language	English
Publishing date	2021-10-16
Publishing country	United States
Document type	Journal Article
ISSN	2589-0042
ISSN (online)	2589-0042
DOI	10.1016/j.isci.2021.103311
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Article ; Online: StraPep: a structure database of bioactive peptides.

Wang, Jian / Yin, Tailang / Xiao, Xuwen / He, Dan / Xue, Zhidong / Jiang, Xinnong / Wang, Yan

Database : the journal of biological databases and curation

2018 Volume 2018

Abstract: Database url: http://isyslab.info/StraPep. ...

Abstract	Database url: http://isyslab.info/StraPep.
MeSH term(s)	Amino Acid Motifs ; Databases, Protein ; Peptides/chemistry ; Peptides/classification ; Peptides/genetics ; Peptides/metabolism ; Protein Processing, Post-Translational
Chemical Substances	Peptides
Language	English
Publishing date	2018-04-24
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2496706-3
ISSN	1758-0463 ; 1758-0463
ISSN (online)	1758-0463
ISSN	1758-0463
DOI	10.1093/database/bay038
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Article ; Online: GABAB1e promotes the malignancy of human cancer cells by targeting the tyrosine phosphatase PTPN12

Bo Wei / Yini Zhu / Peng Yang / Yong Han / Suyun Wang / Xiaomei Wang / Shuai Xia / Xiaoguang Song / Zhongling Zhang / Sheng Wang / Philippe Rondard / Jean-Philippe Pin / Xinnong Jiang / Jianfeng Liu

iScience, Vol 24, Iss 11, Pp 103311- (2021)

2021

Abstract: Summary: Neurotransmitter receptors are involved in cancer progression. Among them, the heterodimeric GABAB receptor, activated by the main inhibitory neurotransmitter GABA, is composed of the transmembrane GABAB1 and GABAB2 subunits. The oncogenic role ... ...

Abstract	Summary: Neurotransmitter receptors are involved in cancer progression. Among them, the heterodimeric GABAB receptor, activated by the main inhibitory neurotransmitter GABA, is composed of the transmembrane GABAB1 and GABAB2 subunits. The oncogenic role of the isoform GABAB1e (GB1e) containing only the extracellular domain of GABAB1 remains unclear. We revealed that GB1e is largely expressed in human breast cancer (BrCa) cell lines as well as in BrCa tissues where it is upregulated. Moreover, GB1e promoted the malignancy of BrCa cells both in vitro and in vivo. We propose that GB1e favors EGFR signaling by interacting with PTPN12 to disrupt the interaction between EGFR and PTPN12, and phosphorylation of Y230 and Y404 on GB1e is required in this process. Our data highlight that the GABBR1 gene through the expression of the GB1e isoform might play an important oncogenic role in BrCa and that GB1e is of interest for the treatment of some cancers.
Keywords	Biological sciences ; Molecular biology ; Neuroscience ; Science ; Q
Language	English
Publishing date	2021-11-01T00:00:00Z
Publisher	Elsevier
Document type	Article ; Online
Database	BASE - Bielefeld Academic Search Engine (life sciences selection)

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Article ; Online: GABA

Xia, Shuai / He, Cong / Zhu, Yini / Wang, Suyun / Li, Huiping / Zhang, Zhongling / Jiang, Xinnong / Liu, Jianfeng

Molecular pharmacology

2017 Volume 92, Issue 3, Page(s) 265–277

Abstract: G protein-coupled receptors (GPCRs) and receptor tyrosine kinases (RTKs) act in concert to regulate cell growth, proliferation, survival, and migration. Metabotropic ... ...

Abstract	G protein-coupled receptors (GPCRs) and receptor tyrosine kinases (RTKs) act in concert to regulate cell growth, proliferation, survival, and migration. Metabotropic GABA
MeSH term(s)	Allosteric Regulation ; Cell Line, Tumor ; Cell Movement ; Extracellular Signal-Regulated MAP Kinases/metabolism ; GTP-Binding Protein alpha Subunits, Gi-Go/physiology ; Humans ; Male ; Neoplasm Invasiveness ; Prostatic Neoplasms/pathology ; Receptor, Epidermal Growth Factor/genetics ; Receptors, GABA-B/physiology ; Transcriptional Activation
Chemical Substances	Receptors, GABA-B ; EGFR protein, human (EC 2.7.10.1) ; Receptor, Epidermal Growth Factor (EC 2.7.10.1) ; Extracellular Signal-Regulated MAP Kinases (EC 2.7.11.24) ; GTP-Binding Protein alpha Subunits, Gi-Go (EC 3.6.5.1)
Language	English
Publishing date	2017-04-19
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	124034-1
ISSN	1521-0111 ; 0026-895X
ISSN (online)	1521-0111
ISSN	0026-895X
DOI	10.1124/mol.116.107854
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Article: Fabrication of a photo-crosslinked gelatin hydrogel for preventing abdominal adhesion

Wu, Wei / Ni, Qing / Xiang, Yi / Dai, Yong / Jiang, Su / Wan, Liping / Liu, Xinnong / Cui, Wenguo

RSC advances. 2016 Sept. 27, v. 6, no. 95

2016

Abstract: Natural hydrogels are promising membranes used to prevent intra-abdominal adhesion formation. Currently, natural hydrogels such as chitosan-, gelatin- or hyaluronic acid-based hydrogels are utilized to prevent adhesion. However, their uncontrollable ... ...

Abstract	Natural hydrogels are promising membranes used to prevent intra-abdominal adhesion formation. Currently, natural hydrogels such as chitosan-, gelatin- or hyaluronic acid-based hydrogels are utilized to prevent adhesion. However, their uncontrollable mechanical properties and quick degradation result in an unsatisfying short effect-time. In this study, a photocrosslinkable gelatin (GelMA) prepolymer was synthesized and developed for preventing intra-abdominal adhesion formation. Hydrogel membranes based on GelMA showed easy-handleability, non-toxic degradation and a long-lasting excellent barrier effect for up to 1 month. We have found that a 20% GelMA hydrogel membrane concentration could be employed to meet the requirements of excellent barrier effect, and the implantation of GelMA hydrogel membranes in rat abdominal cavities in experimental groups led to a considerable decrease in adhesion formation in comparison to the control group. The present study established the initial foundation for a novel and practical approach to prevent abdominal adhesion in surgery.
Keywords	adhesion ; gelatin ; hydrogels ; mechanical properties ; rats ; surgery
Language	English
Dates of publication	2016-0927
Size	p. 92449-92453.
Publishing place	The Royal Society of Chemistry
Document type	Article
ISSN	2046-2069
DOI	10.1039/c6ra21435e
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: Calcium and CaSR/IP3R in prostate cancer development

Liyang Wang / MengMeng Xu / Zhongguang Li / Mengting Shi / Xin Zhou / Xinnong Jiang / Joseph Bryant / Steven Balk / Jianjie Ma / William Isaacs / Xuehong Xu

Cell & Bioscience, Vol 8, Iss 1, Pp 1-

2018 Volume 7

Abstract: Abstract Prostate cancer (PrCa) progression and mortality are associated with calcium metabolism, parathyroid hormone level, and vitamin D level. However, the lack of comprehensive understanding on the molecular rationale of calcium intake, serum ... ...

Abstract	Abstract Prostate cancer (PrCa) progression and mortality are associated with calcium metabolism, parathyroid hormone level, and vitamin D level. However, the lack of comprehensive understanding on the molecular rationale of calcium intake, serum homeostasis, and cytoplasmic function, is critically hindering our ability to propose a mechanism based technique for targeting calcium in PrCa. Recently, studies performed on PrCa samples have shown that calcium-sensing receptor regulates cytoplasmic calcium levels in relation to extracellular calcium concentrations. Recent publications have also revealed the role of BAP1 and FBXL2 associated endoplasmic reticular IP3Rs in controlling the trafficking of calcium from cytosol into the mitochondria of PrCa cells. Competitive binding between BAP1, PTEN and FBXL2 to IP3Rs regulates the calcium flux of mitochondria and thereby controls apoptosis. Analysis of data released by Prostate Adenocarcinoma (Provisional TCGA) reveals that calcium related proteins play critical role in the development of PrCa. From this constantly expanding appreciation for the role of calcium outside the muscle, we predict that calcium-induced-calcium-release ryanodine receptors could also be involved in determining cell fate.
Keywords	Prostate cancer ; CaSR ; RyR ; IP3R ; BAP1 ; FBXL2 ; Biotechnology ; TP248.13-248.65 ; Biology (General) ; QH301-705.5 ; Biochemistry ; QD415-436
Language	English
Publishing date	2018-02-01T00:00:00Z
Publisher	BMC
Document type	Article ; Online
Database	BASE - Bielefeld Academic Search Engine (life sciences selection)

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Article ; Online: Pancreatic ductal adenocarcinoma and chronic mass-forming pancreatitis: Differentiation with dual-energy MDCT in spectral imaging mode.

Yin, Qihua / Zou, Xinnong / Zai, Xiaodong / Wu, Zhiyuan / Wu, Qingyang / Jiang, Xingyu / Chen, Hongwei / Miao, Fei

European journal of radiology

2015 Volume 84, Issue 12, Page(s) 2470–2476

Abstract: Objective: To investigate the value of dual-energy MDCT in spectral imaging in the differential diagnosis of chronic mass-forming chronic pancreatitis (CMFP) and pancreatic ductal adenocarcinoma (PDAC) during the arterial phase (AP) and the pancreatic ... ...

Abstract	Objective: To investigate the value of dual-energy MDCT in spectral imaging in the differential diagnosis of chronic mass-forming chronic pancreatitis (CMFP) and pancreatic ductal adenocarcinoma (PDAC) during the arterial phase (AP) and the pancreatic parenchymal phase (PP). Materials and methods: Thirty five consecutive patients with CMFP (n=15) or PDAC (n=20) underwent dual-energy MDCT in spectral imaging during AP and PP. Iodine concentrations were derived from iodine-based material-decomposition CT images and normalized to the iodine concentration in the aorta. The difference in iodine concentration between the AP and PP, contrast-to-noise ratio (CNR) and the slope K of the spectrum curve were calculated. Results: Normalized iodine concentrations (NICs) in patients with CMFP differed significantly from those in patients with PDAC during two double phases (mean NIC, 0.26±0.04 mg/mL vs. 0.53±0.02 mg/mL, p=0.0001; 0.07±0.02 mg/mL vs. 0.28±0.04 mg/mL, p=0.0002, respectively). There were significant differences in the value of the slope K of the spectrum curve in two groups during AP and PP (K(CMFP)=3.27±0.70 vs. K(PDAC)=1.35±0.41, P=0.001, and K(CMFP)=3.70±0.17 vs. K(PDAC)=2.16±0.70, p=0.003, respectively). CNRs at low energy levels (40-70 keV) were higher than those at high energy levels (80-40 keV). Conclusion: Individual patient CNR-optimized energy level images and the NIC can be used to improve the sensitivity and the specificity for differentiating CMFP from PDAC by use of dual-energy MDCT in spectral imaging with fast tube voltage switching.
MeSH term(s)	Adenocarcinoma/diagnostic imaging ; Aged ; Carcinoma, Pancreatic Ductal/diagnostic imaging ; Contrast Media ; Diagnosis, Differential ; Female ; Humans ; Iodine ; Male ; Middle Aged ; Multidetector Computed Tomography/methods ; Observer Variation ; Pancreatic Neoplasms/diagnostic imaging ; Pancreatitis, Chronic/diagnostic imaging ; ROC Curve ; Radiographic Image Enhancement ; Radiography, Dual-Energy Scanned Projection/methods ; Retrospective Studies ; Sensitivity and Specificity
Chemical Substances	Contrast Media ; Iodine (9679TC07X4)
Language	English
Publishing date	2015-12
Publishing country	Ireland
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	138815-0
ISSN	1872-7727 ; 0720-048X
ISSN (online)	1872-7727
ISSN	0720-048X
DOI	10.1016/j.ejrad.2015.09.023
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Article: Perlecan and tumor angiogenesis.

Jiang, Xinnong / Couchman, John R

The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society

2003 Volume 51, Issue 11, Page(s) 1393–1410

Abstract: Perlecan is a major heparan sulfate proteoglycan (HSPG) of basement membranes (BMs) and connective tissues. The core protein of perlecan is divided into five domains based on sequence homology to other known proteins. Commonly, the N-terminal domain I of ...

Abstract	Perlecan is a major heparan sulfate proteoglycan (HSPG) of basement membranes (BMs) and connective tissues. The core protein of perlecan is divided into five domains based on sequence homology to other known proteins. Commonly, the N-terminal domain I of mammalian perlecan is substituted with three HS chains that can bind a number of matrix molecules, cytokines, and growth factors. Perlecan is essential for metazoan life, as shown by genetic manipulations of nematodes, insects, and mice. There are also known human mutations that can be lethal. In vertebrates, new functions of perlecan emerged with the acquisition of a closed vascular system and skeletal connective tissues. Many of perlecan's functions may be related to the binding and presentation of growth factors to high-affinity tyrosine kinase (TK) receptors. Data are accumulating, as discussed here, that similar growth factor-mediated processes may have unwanted promoting effects on tumor cell proliferation and tumor angiogenesis. Understanding of these attributes at the molecular level may offer opportunities for therapeutic intervention.
MeSH term(s)	Alternative Splicing ; Animals ; Extracellular Matrix/metabolism ; Fibroblast Growth Factor 2/metabolism ; Heparan Sulfate Proteoglycans/chemistry ; Heparan Sulfate Proteoglycans/genetics ; Heparan Sulfate Proteoglycans/metabolism ; Humans ; Neoplasms/blood supply ; Neovascularization, Pathologic/metabolism ; Vascular Endothelial Growth Factor A/metabolism
Chemical Substances	Heparan Sulfate Proteoglycans ; Vascular Endothelial Growth Factor A ; Fibroblast Growth Factor 2 (103107-01-3) ; perlecan (143972-95-6)
Language	English
Publishing date	2003-11
Publishing country	United States
Document type	Journal Article ; Research Support, U.S. Gov't, P.H.S. ; Review
ZDB-ID	218208-7
ISSN	1551-5044 ; 0022-1554
ISSN (online)	1551-5044
ISSN	0022-1554
DOI	10.1177/002215540305101101
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Article ; Online: GABAB receptor complex as a potential target for tumor therapy.

Jiang, Xinnong / Su, Li / Zhang, Qian / He, Cong / Zhang, Zhongling / Yi, Ping / Liu, Jianfeng

The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society

2012 Volume 60, Issue 4, Page(s) 269–279

Abstract: γ-Aminobutyric acid (GABA) is the main inhibitory neurotransmitter in the vertebrate central nervous system. Metabotropic GABA(B) receptors are heterodimeric G-protein-coupled receptors (GPCRs) consisting of GABA(B1) and GABA(B2) subunits. The ... ...

Abstract	γ-Aminobutyric acid (GABA) is the main inhibitory neurotransmitter in the vertebrate central nervous system. Metabotropic GABA(B) receptors are heterodimeric G-protein-coupled receptors (GPCRs) consisting of GABA(B1) and GABA(B2) subunits. The intracellular C-terminal domains of GABA(B) receptors are involved in heterodimerization, oligomerization, and association with other proteins, which results in a large receptor complex. Multiple splice variants of the GABA(B1) subunit have been identified in which GABA(B1a) and GABA(B1b) are the most abundant isoforms in the nervous system. Isoforms GABA(B1c) through GABA(B1n) are minor isoforms and are detectable only at mRNA levels. Some of the minor isoforms have been detected in peripheral tissues and encode putative soluble proteins with C-terminal truncations. Interestingly, increased expression of GABA(B) receptors has been detected in several human cancer cells and tissues. Moreover, GABA(B) receptor agonist baclofen inhibited tumor growth in rat models. GABA(B) receptor activation not only induces suppressing the proliferation and migration of various human tumor cells but also results in inactivation of CREB (cAMP-responsive element binding protein) and ERK in tumor cells. Their structural complexity makes it possible to disrupt the functions of GABA(B) receptors in various ways, raising GABA(B) receptor diversity as a potential therapeutic target in some human cancers.
MeSH term(s)	Animals ; Baclofen/pharmacology ; Cell Movement ; Cell Proliferation ; Dimerization ; GABA Agonists/pharmacology ; Humans ; Neoplasms/metabolism ; Neoplasms/pathology ; Neoplasms/therapy ; Rats ; Receptors, GABA-B/chemistry ; Receptors, GABA-B/metabolism ; Signal Transduction
Chemical Substances	GABA Agonists ; Receptors, GABA-B ; Baclofen (H789N3FKE8)
Language	English
Publishing date	2012-01-20
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Review
ZDB-ID	218208-7
ISSN	1551-5044 ; 0022-1554
ISSN (online)	1551-5044
ISSN	0022-1554
DOI	10.1369/0022155412438105
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Article ; Online: Phosphoinositide 3-kinase pathway activation in phosphate and tensin homolog (PTEN)-deficient prostate cancer cells is independent of receptor tyrosine kinases and mediated by the p110beta and p110delta catalytic subunits.

Jiang, Xinnong / Chen, Sen / Asara, John M / Balk, Steven P

The Journal of biological chemistry

2010 Volume 285, Issue 20, Page(s) 14980–14989

Abstract: Class IA phosphoinositide 3-kinase (PI3K) p110 catalytic subunits are activated upon Src homology 2 domain-mediated binding of their p85 regulatory subunits to tyrosine-phosphorylated pYXXM motifs in receptor tyrosine kinases (RTKs) or adaptor proteins. ... ...

Abstract	Class IA phosphoinositide 3-kinase (PI3K) p110 catalytic subunits are activated upon Src homology 2 domain-mediated binding of their p85 regulatory subunits to tyrosine-phosphorylated pYXXM motifs in receptor tyrosine kinases (RTKs) or adaptor proteins. The PI3K pathway is activated by phosphate and tensin homolog (PTEN) loss in most prostate cancers (PCa), but the contribution of upstream RTKs that may be targeted therapeutically has not been assessed. Immunoblotting of p85-associated proteins in serum-starved PTEN-deficient LNCaP and C4-2 PCa cells showed a small set of discrete tyrosine-phosphorylated proteins, but these proteins were not recognized by an anti-pYXXM motif antibody and were not found in PTEN-deficient PC3 PCa cells. LC/MS/MS using label-free proteomics and immunoblotting showed that p85 was associated primarily with p110beta and p110delta. An interaction with ErbB3 was also detected but was independent of ErbB3 tyrosine phosphorylation and was not required for basal PI3K activity. Basal tyrosine phosphorylation of p110beta and p110delta could be blocked by c-Src inhibitors, but this did not suppress PI3K activity, which was similarly independent of Ras. Basal PI3K activity was mediated by p110beta in PC3 cells and by both p110beta and p110delta in LNCaP cells, whereas p110alpha was required for PI3K activation in response to RTK stimulation by heregulin-beta1. These findings show that basal PI3K activity in PTEN-deficient PCa cells is RTK-independent and can be mediated by p110beta and p110delta. Increased p110beta expression in PCa may be required for RTK-independent PI3K pathway activation in adult prostate epithelium with genetic or epigenetic PTEN down-regulation.
MeSH term(s)	Catalytic Domain ; Cell Line, Tumor ; Chromatography, Liquid ; Enzyme Activation ; Humans ; Male ; PTEN Phosphohydrolase/genetics ; PTEN Phosphohydrolase/physiology ; Phosphatidylinositol 3-Kinases/metabolism ; Phosphorylation ; Prostatic Neoplasms/enzymology ; Prostatic Neoplasms/pathology ; Receptor Protein-Tyrosine Kinases/metabolism ; Tandem Mass Spectrometry
Chemical Substances	Phosphatidylinositol 3-Kinases (EC 2.7.1.-) ; Receptor Protein-Tyrosine Kinases (EC 2.7.10.1) ; PTEN Phosphohydrolase (EC 3.1.3.67) ; PTEN protein, human (EC 3.1.3.67)
Language	English
Publishing date	2010-03-15
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
ZDB-ID	2997-x
ISSN	1083-351X ; 0021-9258
ISSN (online)	1083-351X
ISSN	0021-9258
DOI	10.1074/jbc.M109.085696
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