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Alternatively activated macrophages are associated with metastasis and poor prognosis in prostate adenocarcinoma.交替活化的巨噬细胞与前列腺腺癌的转移和不良预后相关。
Oncol Lett. 2015 Sep;10(3):1390-1396. doi: 10.3892/ol.2015.3400. Epub 2015 Jun 19.
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Focal-adhesion-independent integrin-αv regulation of FAK and c-Myc is necessary for 3D skin formation and tumor invasion.粘着斑非依赖性整合素αv对粘着斑激酶(FAK)和c-Myc的调节对于三维皮肤形成和肿瘤侵袭是必要的。
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Interactions between αv-Integrin and HER2 and Their Role in the Invasive Phenotype of Breast Cancer Cells In Vitro and in Rat Brain.αv整合素与HER2之间的相互作用及其在乳腺癌细胞体外和大鼠脑侵袭表型中的作用
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CDH1 and IL1-beta expression dictates FAK and MAPKK-dependent cross-talk between cancer cells and human mesenchymal stem cells.CDH1和白细胞介素-1β的表达决定了癌细胞与人间充质干细胞之间由黏着斑激酶和丝裂原活化蛋白激酶激酶依赖性的相互作用。
Stem Cell Res Ther. 2015 Jul 24;6(1):135. doi: 10.1186/s13287-015-0123-0.
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Galectin-3 Overrides PTRF/Cavin-1 Reduction of PC3 Prostate Cancer Cell Migration.半乳糖凝集素-3克服了PTRF/Cavin-1对PC3前列腺癌细胞迁移的抑制作用。
PLoS One. 2015 May 5;10(5):e0126056. doi: 10.1371/journal.pone.0126056. eCollection 2015.
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miR-25 Modulates Invasiveness and Dissemination of Human Prostate Cancer Cells via Regulation of αv- and α6-Integrin Expression.miR-25 通过调节αv-和α6-整合素的表达来调节人前列腺癌细胞的侵袭和扩散。
Cancer Res. 2015 Jun 1;75(11):2326-36. doi: 10.1158/0008-5472.CAN-14-2155. Epub 2015 Apr 9.
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MicroRNA miR-125a-3p modulates molecular pathway of motility and migration in prostate cancer cells.微小RNA miR-125a-3p调节前列腺癌细胞的运动和迁移分子途径。
Oncoscience. 2014 Apr 30;1(4):250-261. doi: 10.18632/oncoscience.30. eCollection 2014.
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FAK signaling in human cancer as a target for therapeutics.FAK 信号在人类癌症中的作用及其作为治疗靶点的研究进展。
Pharmacol Ther. 2015 Feb;146:132-49. doi: 10.1016/j.pharmthera.2014.10.001. Epub 2014 Oct 12.
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Correlation between the expression of integrins in prostate cancer and clinical outcome in 1284 patients.1284例前列腺癌患者中整合素表达与临床结局的相关性
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Safety, tolerability, and pharmacokinetics of the novel αv-integrin antibody EMD 525797 (DI17E6) in healthy subjects after ascending single intravenous doses.新型αv整合素抗体EMD 525797(DI17E6)在健康受试者中单次静脉递增剂量给药后的安全性、耐受性和药代动力学。
Invest New Drugs. 2014 Apr;32(2):347-54. doi: 10.1007/s10637-013-0038-5. Epub 2013 Nov 19.

阿比妥珠单抗靶向αV类整合素可抑制前列腺癌进展。

Abituzumab Targeting of αV-Class Integrins Inhibits Prostate Cancer Progression.

作者信息

Jiang Yuan, Dai Jinlu, Yao Zhi, Shelley Greg, Keller Evan T

机构信息

Department of Urology, University of Michigan, Ann Arbor, Michigan.

Department of Immunology, Tianjin Medical University, Tianjin, China.

出版信息

Mol Cancer Res. 2017 Jul;15(7):875-883. doi: 10.1158/1541-7786.MCR-16-0447. Epub 2017 Mar 17.

DOI:10.1158/1541-7786.MCR-16-0447
PMID:28314844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5541673/
Abstract

Integrins that contain an integrin αV subunit contribute to multiple functions that promote cancer progression. The goal of this study was to determine whether abituzumab (DI17E6, EMD 525797), a humanized monoclonal antibody (mAb) against integrin αV impacts, prostate cancer progression. To evaluate this, prostate cancer cells were treated with DI17E6 and its effects on proliferation, apoptosis, cell-cycle, adhesion, detachment, migration, invasion and phosphorylation of downstream targets, including FAK, Akt, and ERK, were determined. DI17E6 promoted detachment and inhibited adhesion of prostate cancer cells to several extracellular matrix (ECM) proteins and cells found in the bone microenvironment but had no impact on cell viability, cell-cycle, and caspase-3/7 activity. DI17E6 inhibited migration and invasion of prostate cancer cells. In addition, DI7E6 decreased phosphorylation of FAK, Akt, and ERK. These results indicate that inhibition of integrin αV with DI17E6 inhibits several prometastatic phenotypes of prostate cancer cells and therefore provide a rationale for further evaluation of DI17E6 for diminishing prostate cancer progression. This work identifies that therapeutic targeting of integrins containing an αV integrin unit inhibits cancer progression and thus may be of clinical benefit. .

摘要

含有整合素αV亚基的整合素有助于促进癌症进展的多种功能。本研究的目的是确定抗整合素αV的人源化单克隆抗体(mAb)abituzumab(DI17E6,EMD 525797)是否会影响前列腺癌进展。为了评估这一点,用DI17E6处理前列腺癌细胞,并确定其对增殖、凋亡、细胞周期、黏附、脱离、迁移、侵袭以及下游靶点(包括FAK、Akt和ERK)磷酸化的影响。DI17E6促进前列腺癌细胞脱离,并抑制其与骨微环境中几种细胞外基质(ECM)蛋白和细胞的黏附,但对细胞活力、细胞周期和半胱天冬酶-3/7活性没有影响。DI17E6抑制前列腺癌细胞的迁移和侵袭。此外,DI7E6降低了FAK、Akt和ERK的磷酸化。这些结果表明,用DI17E6抑制整合素αV可抑制前列腺癌细胞的几种促转移表型,因此为进一步评估DI17E6以减少前列腺癌进展提供了理论依据。这项研究表明,对含有αV整合素单元的整合素进行治疗性靶向可抑制癌症进展,因此可能具有临床益处。