Huang Ying, Li Xihan, Sha Huizi, Zhang Lianru, Bian Xinyu, Han Xiao, Liu Baorui
The Comprehensive Cancer Centre, Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, Nanjing, Jiangsu, P.R. China.
State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, Jiangsu, P.R. China.
Oncol Rep. 2017 Apr;37(4):2063-2070. doi: 10.3892/or.2017.5440. Epub 2017 Feb 10.
KLA (sequence, KLAKLAKKLAKLAK) is a peptide which leads to programmed cell death by disrupting the mitochondrial membrane. However, low penetration in tumors greatly limits its application and efficacy. To develop a KLA-based cancer therapy, KLA-iRGD, a recombinant protein was constructed. It consists of the KLA peptide and iRGD (CRGDKGPDC), a tumor-homing peptide with high penetration into tumor tissue and cells. The conjugated KLA exhibits pro-apoptotic activity to prevent the growth of a tumor once it is inside the cell. Once KLA-iRGD is internalized in cultured tumor cells, via the activation of the receptor neuropilin-1, it spreads extensively throughout the mass of the tumor. The recombinant KLA-iRGD protein showed antitumor activity in vivo in mice and in vitro in tumor cell lines. Repeated treatment with KLA-iRGD greatly prevented tumor growth, resulting in a considerable reduction in tumor volume. According to our data, KLA-iRGD may serve as a potential anticancer agent with limited systemic toxicity and high selectivity for the treatment of MKN45 gastric cancer, which may lead to the enhancement of new targeted anticancer agents.
KLA(序列为KLAKLAKKLAKLAK)是一种通过破坏线粒体膜导致程序性细胞死亡的肽。然而,其在肿瘤中的低渗透性极大地限制了其应用和疗效。为了开发基于KLA的癌症治疗方法,构建了一种重组蛋白KLA-iRGD。它由KLA肽和iRGD(CRGDKGPDC)组成,iRGD是一种能高效渗透进入肿瘤组织和细胞的肿瘤归巢肽。一旦结合的KLA进入细胞内,就会表现出促凋亡活性以阻止肿瘤生长。一旦KLA-iRGD在培养的肿瘤细胞中内化,通过激活神经纤毛蛋白-1受体,它会在整个肿瘤块中广泛扩散。重组KLA-iRGD蛋白在小鼠体内和肿瘤细胞系体外均显示出抗肿瘤活性。用KLA-iRGD重复治疗可极大地抑制肿瘤生长,导致肿瘤体积显著减小。根据我们的数据,KLA-iRGD可能作为一种潜在的抗癌药物,具有有限的全身毒性和对MKN45胃癌的高选择性,这可能会促进新型靶向抗癌药物的研发。