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本文引用的文献

1
Expression of autotaxin and lysophosphatidic acid receptors increases mammary tumorigenesis, invasion, and metastases.自分泌运动因子和溶血磷脂酸受体的表达会增加乳腺肿瘤发生、侵袭及转移。
Cancer Cell. 2009 Jun 2;15(6):539-50. doi: 10.1016/j.ccr.2009.03.027.
2
Cancer statistics, 2009.2009年癌症统计数据。
CA Cancer J Clin. 2009 Jul-Aug;59(4):225-49. doi: 10.3322/caac.20006. Epub 2009 May 27.
3
Molecular targets for treatment of inflammatory breast cancer.炎性乳腺癌治疗的分子靶点
Nat Rev Clin Oncol. 2009 Jul;6(7):387-94. doi: 10.1038/nrclinonc.2009.73. Epub 2009 May 26.
4
The biology of ovarian cancer: new opportunities for translation.卵巢癌生物学:转化医学的新机遇
Nat Rev Cancer. 2009 Jun;9(6):415-28. doi: 10.1038/nrc2644.
5
Lysophosphatidic acid-induced transcriptional profile represents serous epithelial ovarian carcinoma and worsened prognosis.溶血磷脂酸诱导的转录谱代表浆液性上皮性卵巢癌且预后较差。
PLoS One. 2009;4(5):e5583. doi: 10.1371/journal.pone.0005583. Epub 2009 May 15.
6
Identification and characterization of a novel lysophosphatidic acid receptor, p2y5/LPA6.一种新型溶血磷脂酸受体p2y5/LPA6的鉴定与特性分析
J Biol Chem. 2009 Jun 26;284(26):17731-41. doi: 10.1074/jbc.M808506200. Epub 2009 Apr 22.
7
The absence of LPA2 attenuates tumor formation in an experimental model of colitis-associated cancer.在结肠炎相关癌症的实验模型中,LPA2的缺失会减弱肿瘤形成。
Gastroenterology. 2009 May;136(5):1711-20. doi: 10.1053/j.gastro.2009.01.002. Epub 2009 Jan 9.
8
Role of acylglycerol kinase in LPA-induced IL-8 secretion and transactivation of epidermal growth factor-receptor in human bronchial epithelial cells.酰基甘油激酶在溶血磷脂酸诱导人支气管上皮细胞分泌白细胞介素-8及表皮生长因子受体反式激活中的作用
Am J Physiol Lung Cell Mol Physiol. 2009 Mar;296(3):L328-36. doi: 10.1152/ajplung.90431.2008. Epub 2008 Dec 26.
9
Lysophosphatidic acid receptors determine tumorigenicity and aggressiveness of ovarian cancer cells.溶血磷脂酸受体决定卵巢癌细胞的致瘤性和侵袭性。
J Natl Cancer Inst. 2008 Nov 19;100(22):1630-42. doi: 10.1093/jnci/djn378. Epub 2008 Nov 11.
10
Identification of small-molecule inhibitors of autotaxin that inhibit melanoma cell migration and invasion.鉴定抑制黑色素瘤细胞迁移和侵袭的自分泌运动因子小分子抑制剂。
Mol Cancer Ther. 2008 Oct;7(10):3352-62. doi: 10.1158/1535-7163.MCT-08-0463.

ATX-LPA 受体轴在炎症和癌症中的作用。

ATX-LPA receptor axis in inflammation and cancer.

机构信息

Department of Systems Biology, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.

出版信息

Cell Cycle. 2009 Nov 15;8(22):3695-701. doi: 10.4161/cc.8.22.9937. Epub 2009 Nov 27.

DOI:10.4161/cc.8.22.9937
PMID:19855166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4166520/
Abstract

Lysophosphatidic acid (LPA, 1- or 2-acyl-sn-glycerol 3-phosphate) mediates a plethora of physiological and pathological activities via interactions with a series of high affinity G protein-coupled receptors (GPCR). Both LPA receptor family members and autotaxin (ATX/LysoPLD), the primary LPA-producing enzyme, are aberrantly expressed in many human breast cancers and several other cancer lineages. Using transgenic mice expressing either an LPA receptor or ATX, we recently demonstrated that the ATX-LPA receptor axis plays a causal role in breast tumorigenesis and cancer-related inflammation, further validating the ATX-LPA receptor axis as a rich therapeutic target in cancer.

摘要

溶血磷脂酸(LPA,1-或 2-酰基-sn-甘油 3-磷酸)通过与一系列高亲和力 G 蛋白偶联受体(GPCR)相互作用,介导多种生理和病理活性。LPA 受体家族成员和自分泌运动因子(ATX/LysoPLD),即主要的 LPA 产生酶,在许多人类乳腺癌和其他几种癌症谱系中异常表达。使用表达 LPA 受体或 ATX 的转基因小鼠,我们最近证明 ATX-LPA 受体轴在乳腺癌发生和癌症相关炎症中起因果作用,进一步验证了 ATX-LPA 受体轴作为癌症的一个丰富治疗靶点。