Jiang Yuan, Dai Jinlu, Yao Zhi, Shelley Greg, Keller Evan T
Department of Urology, University of Michigan, Ann Arbor, Michigan.
Department of Immunology, Tianjin Medical University, Tianjin, China.
Mol Cancer Res. 2017 Jul;15(7):875-883. doi: 10.1158/1541-7786.MCR-16-0447. Epub 2017 Mar 17.
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. .
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。