Hsieh Ya-Ju, Tseng Sung-Pin, Kuo Yu-Hsuan, Cheng Tain-Lu, Chiang Chiao-Yu, Tzeng Yew-Min, Tsai Wan-Chi
Department of Medical Imaging and Radiological Sciences, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Department of Medical Laboratory Science and Biotechnology, Kaohsiung Medical University, Kaohsiung 80708, Taiwan; Department of Laboratory Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Evid Based Complement Alternat Med. 2016;2016:8680372. doi: 10.1155/2016/8680372. Epub 2016 May 8.
Pancreatic cancer is the eighth leading cause of cancer death worldwide. Patients with pancreatic cancer are normally diagnosed at an advanced stage and present poor survival rate. Ovatodiolide (OV), a bioactive macrocyclic diterpenoid isolated from Anisomeles indica, showed cytotoxicity effects in pancreatic cancer cells by inhibiting cell proliferation and inducing apoptosis. Moreover, not only were cell adhesion and invasion markedly suppressed in a dose-dependent manner, but the mRNA expression of matrix metalloproteinase-9 (MMP-9) and focal adhesion kinase (FAK) was also significantly decreased. Western blot analysis indicated that OV potently suppressed the phosphorylation of STAT-3 and its upstream kinase including ERK1/2, P38, and AKT Ser473. Meanwhile, OV inactivated the nuclear factor kappa B (NF-κB) by inhibiting IκB kinase (IKK α/β) activation and the subsequent suppression of inhibitor of kappa B (IκB) phosphorylation. These results demonstrated that OV could potentially inhibit Mia-PaCa2 cancer cells proliferation and induce apoptosis through modulation of NF-κB and STAT3 pathway. Moreover, OV suppressed cell invasiveness and interfered with cell-matrix adhesion in Mia-PaCa2 cancer cells by reducing MMP-9 and FAK transcription through suppressing NF-κB and STAT3 pathway. Taken together, our findings reveal a new therapeutic and antimetastatic potential of ovatodiolide for pancreatic cancer remedy.
胰腺癌是全球第八大致癌死亡原因。胰腺癌患者通常在晚期被诊断出来,生存率较低。卵叶二萜内酯(OV)是从广防风中分离出的一种具有生物活性的大环二萜类化合物,通过抑制细胞增殖和诱导凋亡对胰腺癌细胞显示出细胞毒性作用。此外,细胞黏附和侵袭不仅以剂量依赖的方式显著受到抑制,基质金属蛋白酶-9(MMP-9)和黏着斑激酶(FAK)的mRNA表达也显著降低。蛋白质免疫印迹分析表明,OV能有效抑制STAT-3及其上游激酶(包括ERK1/2、P38和AKT Ser473)的磷酸化。同时,OV通过抑制IκB激酶(IKKα/β)的激活以及随后对κB抑制蛋白(IκB)磷酸化的抑制,使核因子κB(NF-κB)失活。这些结果表明,OV可能通过调节NF-κB和STAT3信号通路来抑制Mia-PaCa2癌细胞的增殖并诱导其凋亡。此外,OV通过抑制NF-κB和STAT3信号通路减少MMP-9和FAK的转录,从而抑制Mia-PaCa2癌细胞的侵袭性并干扰细胞与基质的黏附。综上所述,我们的研究结果揭示了卵叶二萜内酯在胰腺癌治疗方面具有新的治疗和抗转移潜力。