IL-8 induces exocytosis of arginase 1 by neutrophil polymorphonuclears in nonsmall cell lung cancer. - Wikidata - wikimedia - TriplyDB

IL-8 induces exocytosis of arginase 1 by neutrophil polymorphonuclears in nonsmall cell lung cancer.

IL-8 induces exocytosis of arginase 1 by neutrophil polymorphonuclears in nonsmall cell lung cancer.

http://www.wikidata.org/entity/Q34980354

about

The IL-8/IL-8R Axis: A Double Agent in Tumor Immune Resistance Neutrophils in Cancer: Two Sides of the Same Coin The CXCL8-CXCR1/2 pathways in cancer Immunosuppression through constitutively activated NF-κB signalling in human ovarian cancer and its reversal by an NF-κB inhibitor.Neutrophils in the tumor microenvironment: trying to heal the wound that cannot heal.Tumor progression stage and anatomical site regulate tumor-associated macrophage and bone marrow-derived monocyte polarization.Myeloid derived suppressor cells (MDSCs) are increased and exert immunosuppressive activity together with polymorphonuclear leukocytes (PMNs) in chronic myeloid leukemia patients.Neutrophils infiltration in the tongue squamous cell carcinoma and its correlation with CEACAM1 expression on tumor cells.Differential transcriptomic analysis of spontaneous lung tumors in B6C3F1 mice: comparison to human non-small cell lung cancer.Tumor-Derived CXCL1 Promotes Lung Cancer Growth via Recruitment of Tumor-Associated Neutrophils Prognostic models to predict survival in patients with advanced non-small cell lung cancer treated with first-line chemo- or targeted therapy Virus-stimulated neutrophils in the tumor microenvironment enhance T cell-mediated anti-tumor immunity.Immune alterations and emerging immunotherapeutic approaches in lung cancer.Protumor and antitumor functions of neutrophil granulocytes.Metabolism of L-arginine by myeloid-derived suppressor cells in cancer: mechanisms of T cell suppression and therapeutic perspectives.The multifaceted functions of neutrophils.Myeloid-derived suppressor cells in glioma.Combination of cancer immunotherapy with clinically available drugs that can block immunosuppressive cells.Small-molecule arginase inhibitors.Metabolism via Arginase or Nitric Oxide Synthase: Two Competing Arginine Pathways in Macrophages Neutrophils: important contributors to tumor progression and metastasis.Neutrophils in the Tumor Microenvironment.Neutrophils in cancer.Leukocyte-mediated Delivery of Nanotherapeutics in Inflammatory and Tumor Sites.IL-10 and ARG-1 concentrations in bone marrow and peripheral blood of metastatic neuroblastoma patients do not associate with clinical outcome.Radiotherapy induces an immediate inflammatory reaction in malignant glioma: a clinical microdialysis study.Increased circulating myeloid-derived suppressor cells correlate with cancer stages, interleukin-8 and -6 in prostate cancer.Inhibition of arginase by CB-1158 blocks myeloid cell-mediated immune suppression in the tumor microenvironment.Phagocyte-extracellular matrix crosstalk empowers tumor development and dissemination.Tumor-associated neutrophils induce apoptosis of non-activated CD8 T-cells in a TNFα and NO-dependent mechanism, promoting a tumor-supportive environment.Induced arginine transport via cationic amino acid transporter-1 is necessary for human T-cell proliferation.Prognostic significance of the ratio of absolute neutrophil count to absolute lymphocyte count in classic Hodgkin lymphoma.Tumor-associated neutrophils suppress pro-tumoral IL-17+ γδ T cells through induction of oxidative stress.CD45+CD33lowCD11bdim myeloid-derived suppressor cells suppress CD8+ T cell activity via the IL-6/IL-8-arginase I axis in human gastric cancer.Macrophages, Neutrophils, and Cancer: A Double Edged Sword Turn Back the TIMe: Targeting Tumor Infiltrating Myeloid Cells to Revert Cancer Progression

P2860

Q26746986-35A95452-0E86-4BFC-8814-B52464931914 Q26773072-226798BD-76CE-4F2B-8F50-0F53F961DB81 Q28075994-8002D554-C06C-444F-BFD6-ABF20AFE51F8 Q33750160-DA3BBD04-8E8C-40DB-A20F-77595F0AF5B2 Q33816141-EF1FF25D-5F80-47E5-87E8-F55B3BD202F6 Q33882555-50508DEF-E72F-44D8-A908-9120A7515369 Q33889439-9575D41C-5C86-4E65-BB7C-798944741E6F Q35108514-B7308FC8-7EB0-4D71-923F-B7F34289E0C7 Q36706060-0FE4D78E-13BF-4B01-B0DC-62D69B8E9336 Q37089248-CC316981-A198-49A8-8528-51993CE9DFCC Q37295840-3B97F582-CE53-44ED-9D9D-15AA692633F4 Q37520497-17551C68-8EEA-4D50-8930-72ECFD137D8F Q38007549-3BA2AC26-00A3-4AB1-81FF-D1B75BCC41FF Q38046098-FCA2CD68-CD79-4811-A9EC-3F796444A98C Q38047050-51EB6F69-C769-4B4C-BC72-8A3422593C90 Q38139589-CD4F9509-3549-4B22-8953-F8552FC9EB9A Q38161536-DE66643E-7CCD-4818-8D61-7C9F47214519 Q38167887-C1062246-FE13-47D9-9C6D-08271E55BC7F Q38172656-7EC8CBBC-5FCB-4A8A-9E01-701BB31E5587 Q38266887-CB8505A2-2F33-4588-9757-A034D380E643 Q38585102-C7746E50-1E56-4E0F-A869-6B76252B2BDC Q38678088-6742EC01-AF1D-4177-B704-C6DE1117FB65 Q38936555-F70187E6-11F6-4771-9BD6-49C7E6429965 Q39159035-8B358800-C0D9-40F9-8859-1115DE1F3A2D Q40190430-5748AA05-ABE0-4BBF-ABF8-EE02B080A405 Q41820198-6A0362A1-A598-4DA5-AC61-F6EA3BBFC64A Q43015717-95938622-517B-4F8C-A70B-189282D73926 Q47146426-74478844-3612-4B57-85C1-25719E0E5889 Q47437633-3C13AC33-020E-4C70-9240-1839545BFE46 Q50424573-9F4A0D69-7AB7-4596-8423-2677B2E853A9 Q50703292-C96B4E21-CE27-4ADF-8F83-957A02253C33 Q53120585-90ED8796-1EB2-4B95-80ED-950307D8E8D2 Q55044228-AF90E4BF-9036-4228-9DBF-572AED5B1024 Q55691199-353F4F29-2290-45F9-87CF-21DDA4E38724 Q56942176-8D8011EA-CF40-4A5C-B19B-6F90F08E11E0 Q58780996-BA141A68-662A-4462-B2A9-870B28393B84

P2860

IL-8 induces exocytosis of arginase 1 by neutrophil polymorphonuclears in nonsmall cell lung cancer.

http://www.wikidata.org/entity/Q34980354

description

2009 nî lūn-bûn

@nan

2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@ast

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@en

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@nl

type

label

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@ast

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@en

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@nl

prefLabel

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@ast

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@en

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@nl

P1433

Q34980354-AA85C2AE-6697-4B36-BE34-30ACBCAFAF41

P1476

Q34980354-604755F2-B7C0-404A-9C65-0619E47FE06B

P2093

Q34980354-2C03BC61-B4B9-4E08-B3EC-50E4544ED977

Q34980354-3206D00F-3C62-4951-B2C8-DB537FD9E501

Q34980354-44810F0B-4284-4C98-8B30-DECF56D459F2

Q34980354-D596D8DB-8CA9-4642-A7A5-6700609535F3

Q34980354-E8AD22F3-491B-466A-B0D6-1B2E57507184

Q34980354-EED3BC89-7E9F-4574-AD94-F8BD9629D80C

P2860

Q34980354-70CF9DB2-24BD-453D-8670-06C7C21039E1

Q34980354-AFE2F48F-F16C-4032-8743-C4B2C35C909C

Q34980354-CE28012D-4A16-4382-9F0B-F2D2A77E1077

Q34980354-EF50FCD2-0A96-4202-AE38-4D42EF168AE6

P304

Q34980354-8A29631D-FCF1-4627-A70B-4A34037E19F1

P31

Q34980354-4F489845-0223-4B62-A157-8D423E99DD52

P356

Q34980354-EE99A132-49A6-4748-B895-BC4D04C75AA6

P433

Q34980354-B64B0DD0-0CF0-4C1C-AB67-B69FA357A1E5

P478

Q34980354-75127A8A-3C3E-4E3E-AC7F-BF9B63C451D1

P50

Q34980354-173EA6D4-DFFE-4A78-8D2E-A2DD08986B97

Q34980354-19E1E6C7-94E1-4C92-8D36-FB4BF2ABBCD3

Q34980354-26BC896A-626D-406C-8284-6AF405A7475A

Q34980354-DC4794A0-A762-4927-83CF-1CFA2A0572F5

P577

Q34980354-52898E71-D3C4-4642-95F8-0117A5D0C57B

P5875

Q34980354-70F4D1D7-72DC-450D-A8AA-073DAFAABB2E

P698

Q34980354-D9BE7016-B498-4C7A-9C83-7EB28D50AF33

P921

Q34980354-D78F8954-85D8-4FD9-80C0-FA3A27648F97

P356

P1433

International Journal of Cancer

P1476

IL-8 induces exocytosis of arg ...... in nonsmall cell lung cancer.

@en

P2093

Anna Maria Orengo

http://www.w3.org/2001/XMLSchema#string

Gaia Barisione

http://www.w3.org/2001/XMLSchema#string

Mauro Truini

http://www.w3.org/2001/XMLSchema#string

Ottavia Barbieri

http://www.w3.org/2001/XMLSchema#string

Rita Rotondo

http://www.w3.org/2001/XMLSchema#string

Roberta Costa

http://www.w3.org/2001/XMLSchema#string

P2860

IL-4-induced arginase 1 suppresses alloreactive T cells in tumor-bearing mice.

L-arginine consumption by macrophages modulates the expression of CD3 zeta chain in T lymphocytes.

Interleukin-8 messenger ribonucleic acid expression correlates with tumor progression, tumor angiogenesis, patient survival, and timing of relapse in non-small-cell lung cancer.

Remission of hepatocellular carcinoma with arginine depletion induced by systemic release of endogenous hepatic arginase due to transhepatic arterial embolisation, augmented by high-dose insulin: arginase as a potential drug candidate for hepatocell

P304

887-893

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/IJC.24448

http://www.w3.org/2001/XMLSchema#string

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

125

http://www.w3.org/2001/XMLSchema#string

P50

Silvano Ferrini

Francesco Grossi

P577

2009-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

24416713

http://www.w3.org/2001/XMLSchema#string

P698

19431148

http://www.w3.org/2001/XMLSchema#string

P921