JP2016088926A5 - - Google Patents

Download PDF

Info

Publication number
JP2016088926A5
JP2016088926A5 JP2015043590A JP2015043590A JP2016088926A5 JP 2016088926 A5 JP2016088926 A5 JP 2016088926A5 JP 2015043590 A JP2015043590 A JP 2015043590A JP 2015043590 A JP2015043590 A JP 2015043590A JP 2016088926 A5 JP2016088926 A5 JP 2016088926A5
Authority
JP
Japan
Prior art keywords
ikaros
inflammatory
substance
test substance
inflammation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2015043590A
Other languages
Japanese (ja)
Other versions
JP6653120B2 (en
JP2016088926A (en
Filing date
Publication date
Application filed filed Critical
Publication of JP2016088926A publication Critical patent/JP2016088926A/en
Publication of JP2016088926A5 publication Critical patent/JP2016088926A5/ja
Application granted granted Critical
Publication of JP6653120B2 publication Critical patent/JP6653120B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Claims (16)

IKAROS(IKZF1)阻害剤を含む、抗炎症薬。 An anti-inflammatory agent comprising an IKAROS (IKZF1) inhibitor. 前記IKAROS阻害剤は、PGE2、抗IKAROS siRNA、および抗IKAROS抗体からなる群より選択される、請求項1に記載の抗炎症薬。 The anti-inflammatory drug according to claim 1, wherein the IKAROS inhibitor is selected from the group consisting of PGE2, anti-IKAROS siRNA, and anti-IKAROS antibody. 前記抗炎症薬は、上皮組織を標的とするものである、請求項1〜2のいずれか1項に記載の抗炎症薬。 The anti-inflammatory agent according to any one of claims 1 to 2, wherein the anti-inflammatory agent targets epithelial tissue. 前記炎症は、IKAROSに起因する上皮が関与する炎症である、請求項1〜3のいずれか1項に記載の抗炎症薬。 The anti-inflammatory drug according to any one of claims 1 to 3, wherein the inflammation is inflammation involving an epithelium caused by IKAROS. 局所投与剤である、請求項1〜4のいずれか1項に記載の抗炎症薬。 The anti-inflammatory agent according to any one of claims 1 to 4 , which is a topical administration agent. 前記抗炎症薬は、皮膚または粘膜組織における炎症の処置または予防のためのものである、請求項1〜5のいずれか1項に記載の抗炎症薬。 The anti-inflammatory drug according to any one of claims 1 to 5, wherein the anti-inflammatory drug is for treatment or prevention of inflammation in skin or mucosal tissue. 以下の(1)〜(3)の工程:
(1)IKAROS遺伝子もしくは該当遺伝子の転写調節領域の制御下にあるレポータータンパク質をコードする核酸を含む細胞を、被検物質に接触させる工程;
(2)前記細胞におけるIKAROS遺伝子もしくはIKAROSタンパク質またはレポータータンパク質の発現量を測定する工程;および
(3)被検物質の非存在下において測定した場合と比較して、IKAROS遺伝子もしくはIKAROSタンパク質またはレポータータンパク質の発現量を低下させた被検物質を、抗炎症性物質の候補として選択する工程
を含む、抗炎症性物質のスクリーニング方法。
The following steps (1) to (3):
(1) contacting a cell containing a nucleic acid encoding a reporter protein under the control of the IKAROS gene or the transcriptional regulatory region of the gene of interest with a test substance;
(2) a step of measuring the expression level of an IKAROS gene or an IKAROS protein or reporter protein in the cell; and (3) an IKAROS gene or an IKAROS protein or a reporter protein as compared with a case where measurement is performed in the absence of a test substance. A method for screening an anti-inflammatory substance, comprising a step of selecting a test substance having a reduced expression level of as a candidate for an anti-inflammatory substance.
IKAROSと被検物質とを接触させ、IKAROSと結合能を有する被検物質を抗炎症性物質の候補として選択することを特徴とする、抗炎症性物質のスクリーニング方法。   A method for screening an anti-inflammatory substance, which comprises contacting an IKAROS and a test substance and selecting a test substance capable of binding to IKAROS as a candidate for the anti-inflammatory substance. 以下の(1)〜(3)の工程:
(1)炎症性疾患の標的細胞を、IKAROSの存在下および非存在下で被検物質に接触させる工程;
(2)各条件下での前記細胞における炎症反応の程度を測定する工程;および
(3)被検物質の非存在下において測定した場合と比較して、IKAROSの存在下で炎症反応を抑制し、IKAROSの非存在下で炎症反応を抑制しなかった被検物質を、IKAROSの機能を阻害して抗炎症作用を示す物質の候補として選択する工程
を含む、抗炎症性物質のスクリーニング方法。
The following steps (1) to (3):
(1) a step of contacting a target cell of an inflammatory disease with a test substance in the presence and absence of IKAROS;
(2) a step of measuring the degree of inflammatory reaction in the cells under each condition; and (3) suppressing the inflammatory reaction in the presence of IKAROS as compared to the case of measuring in the absence of the test substance. A method for screening an anti-inflammatory substance, comprising a step of selecting a test substance that did not suppress an inflammatory reaction in the absence of IKAROS as a candidate for a substance that inhibits the function of IKAROS and exhibits an anti-inflammatory action.
polyI:C、インターロイキン−Iα(IL−1α)、腫瘍壊死因子(TNF)αまたはH2O2刺激により炎症反応を惹起することを特徴とする、請求項9に記載の方法。   The method according to claim 9, wherein an inflammatory response is induced by stimulation with polyI: C, interleukin-Iα (IL-1α), tumor necrosis factor (TNF) α or H 2 O 2. 前記細胞が、上皮細胞を含む、請求項7、9または10のいずれか1項に記載の方法。   11. A method according to any one of claims 7, 9 or 10, wherein the cells comprise epithelial cells. 前記炎症は、IKAROSに起因する上皮が関与する炎症である、請求項7〜11のいずれか1項に記載の方法。 The method according to any one of claims 7 to 11, wherein the inflammation is inflammation involving epithelium caused by IKAROS. polyI:Cを含む、IKAROS遺伝子の発現上昇または誘導のための組成物。 A composition for increasing or inducing IKAROS gene expression, comprising polyI: C. IKAROS遺伝子の発現が上昇または誘導された、単離細胞。 An isolated cell in which expression of the IKAROS gene is increased or induced. IKAROS遺伝子の発現が上昇または誘導された、炎症モデル動物。 An inflammation model animal in which expression of the IKAROS gene is increased or induced. 前記炎症モデル動物は、皮膚組織および粘膜組織からなる群より選択される少なくとも1つに細胞浸潤がみられる、請求項15に記載の炎症モデル動物。 The inflammation model animal according to claim 15, wherein the inflammation model animal has cell infiltration in at least one selected from the group consisting of skin tissue and mucosal tissue.
JP2015043590A 2014-10-31 2015-03-05 Anti-inflammatory drugs based on IKAROS inhibition Active JP6653120B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2014223295 2014-10-31
JP2014223295 2014-10-31

Publications (3)

Publication Number Publication Date
JP2016088926A JP2016088926A (en) 2016-05-23
JP2016088926A5 true JP2016088926A5 (en) 2018-03-22
JP6653120B2 JP6653120B2 (en) 2020-02-26

Family

ID=56017549

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015043590A Active JP6653120B2 (en) 2014-10-31 2015-03-05 Anti-inflammatory drugs based on IKAROS inhibition

Country Status (1)

Country Link
JP (1) JP6653120B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111961702A (en) * 2020-07-22 2020-11-20 上海珈蓓生物科技有限公司 Cytological evaluation method for anti-skin infectious inflammatory reaction of plant extract and application thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0625159B1 (en) * 1992-09-14 2003-03-26 The General Hospital Corporation Ikaros: a regulatory gene involved in t-cell differentiation
JPH1029942A (en) * 1996-04-02 1998-02-03 Yoichi Ichikawa Therapeutic agent for chronic arthrorheumatism
CA2737219C (en) * 2008-08-11 2017-02-28 Tracy Keller Halofuginone analogs for inhibition of trna synthetases and uses thereof
WO2014004990A2 (en) * 2012-06-29 2014-01-03 Celgene Corporation Methods for determining drug efficacy using cereblon-associated proteins
US10272117B2 (en) * 2014-02-24 2019-04-30 Celgene Corporation Methods of using an activator of cereblon for neural cell expansion and the treatment of central nervous system disorders

Similar Documents

Publication Publication Date Title
Shao et al. Nuclear IL-33 regulates soluble ST2 receptor and IL-6 expression in primary human arterial endothelial cells and is decreased in idiopathic pulmonary arterial hypertension
Puxeddu et al. Free IL-18 and IL-33 cytokines in chronic spontaneous urticaria
JP2017510552A5 (en)
EA201201640A1 (en) METHODS FOR DETERMINING CANCER STABILITY TO INHIBITORS HISTONEDEISETHYLASE
JP2014144959A5 (en)
WO2015176066A3 (en) Lpa-associated protein and rna expression
van der Pouw Kraan et al. Systemic toll-like receptor and interleukin-18 pathway activation in patients with acute ST elevation myocardial infarction
JP2015521728A5 (en)
Liu et al. HMGB1 translocation and expression is caused by warm ischemia reperfusion injury, but not by partial hepatectomy in rats
Kwak et al. Quantitative evaluation of therapeutic effect of Liriope platyphylla on phthalic anhydride-induced atopic dermatitis in IL-4/Luc/CNS-1 Tg mice
JP2013527437A5 (en)
JP2016528914A5 (en)
Wong et al. The LIM-only protein FHL2 regulates interleukin-6 expression through p38 MAPK mediated NF-κB pathway in muscle cells
Caselli Inflammation in cardiac disease: focus on Interleukin-33/ST2 pathway
JP2016088926A5 (en)
Corporan et al. Hemodynamic and transcriptomic studies suggest early left ventricular dysfunction in a preclinical model of severe mitral regurgitation
Gibbert et al. YB-1 increases glomerular, but decreases interstitial fibrosis in CNI-induced nephropathy
Mahmutovic-Persson et al. Capacity of capsazepinoids to relax human small airways and inhibit TLR3-induced TSLP and IFNβ production in diseased bronchial epithelial cells
JP2016511822A5 (en)
Song et al. Valproic acid attenuates the expression of pro-inflammatory cytokines lipopolysaccharide-treated canine peripheral blood mononuclear cells (in vitro) and in a canine endotoxemia model (in vivo)
JP2016520563A5 (en)
JP2015520744A5 (en)
JP2016531843A5 (en)
Hattori et al. FR-167653, a selective p38 MAPK inhibitor, exerts salutary effect on liver cirrhosis through downregulation of Runx2
Wang et al. Interaction between interleukin‑6 and angiotensin II receptor 1 in the hypothalamic paraventricular nucleus contributes to progression of heart failure