Amin Hina, Wani Naiem Ahmad, Farooq Saleem, Nayak Debasis, Chakraborty Souneek, Shankar Sudha, Rasool Reyaz Ur, Koul Surinder, Goswami Anindya, Rai Rajkishor
Cancer Pharmacology Division, Medicinal Chemistry Division, and Bioorganic Chemistry Division, CSIR-Indian Institute of Integrative Medicine , Canal Road, Jammu Tawi, J&K 180001, India.
ACS Med Chem Lett. 2015 Aug 31;6(10):1071-4. doi: 10.1021/acsmedchemlett.5b00257. eCollection 2015 Oct 8.
The present work describes the anti-invasive effect of conjugate BC06, a novel conjugate of EPA, (2E,4E)-4-(benzo[d][1,3]dioxol-5-ylmethylene) hex-2-enoic acid with β,β-disubstituted-β-amino acid, β(3,3)-Pip-OH (2-(4-aminopiperidin-4-yl)acetic acid), in human pancreatic carcinoma. The conjugate BC06 inhibited invasion and migration of PANC-1 cells in wound healing, matrigel invasion, and gelatin degradation assays. Apart from suppressing PI3K/Akt/NF-kB signaling, which is involved in the up-regulation of matrix metalloproteinases, our study also demonstrated that dose-dependent treatment of BC06 results in the upregulation of TIMP-1 and E-cadherin expression. Further, BC06 was found to be inhibiting the metastatic ability of PANC-1 cells by reducing MMP-2 and MMP-9 expression. These findings suggest that EPA conjugate with β(3,3)-Pip-OH, BC06, may be used as an anti-invasive agent against human pancreatic carcinoma.
本研究描述了共轭物BC06的抗侵袭作用,BC06是一种新型共轭物,由二十碳五烯酸(EPA)、(2E,4E)-4-(苯并[d][1,3]二氧杂环戊烯-5-基亚甲基)己-2-烯酸与β,β-二取代-β-氨基酸β(3,3)-Pip-OH(2-(4-氨基哌啶-4-基)乙酸)组成,用于研究其对人胰腺癌的作用。共轭物BC06在伤口愈合、基质胶侵袭和明胶降解试验中抑制了PANC-1细胞的侵袭和迁移。除了抑制参与基质金属蛋白酶上调的PI3K/Akt/NF-κB信号通路外,我们的研究还表明,BC06的剂量依赖性治疗导致TIMP-1和E-钙黏蛋白表达上调。此外,发现BC06通过降低MMP-2和MMP-9的表达来抑制PANC-1细胞的转移能力。这些发现表明,EPA与β(3,3)-Pip-OH的共轭物BC06可能用作抗人胰腺癌的抗侵袭剂。