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相思子凝集素是一种对人类乳腺癌具有强大抗增殖和抗血管生成作用的药剂。

Abrus agglutinin is a potent anti-proliferative and anti-angiogenic agent in human breast cancer.

作者信息

Bhutia Sujit K, Behera Birendra, Nandini Das Durgesh, Mukhopadhyay Subhadip, Sinha Niharika, Panda Prashanta Kumar, Naik Prajna Paramita, Patra Samir K, Mandal Mahitosh, Sarkar Siddik, Menezes Mitchell E, Talukdar Sarmistha, Maiti Tapas K, Das Swadesh K, Sarkar Devanand, Fisher Paul B

机构信息

Department of Life Science, National Institute of Technology, Rourkela, India.

Department of Biotechnology, Indian Institute of Technology, Kharagpur, India.

出版信息

Int J Cancer. 2016 Jul 15;139(2):457-66. doi: 10.1002/ijc.30055. Epub 2016 Mar 30.

Abstract

Abrus agglutinin (AGG), a plant lectin isolated from the seeds of Abrus precatorius, has documented antitumor and immunostimulatory effects in murine models. To examine possible antitumor activity against breast cancer, we established human breast tumor xenografts in athymic nude mice and intraperitoneally administered AGG. AGG inhibited tumor growth and angiogenesis as confirmed by monitoring the expression of Ki-67 and CD-31, respectively. In addition, TUNEL positive cells increased in breast tumors treated with AGG suggesting that AGG mediates anti-tumorigenic activity through induction of apoptosis and inhibition of angiogenesis. On a molecular level, AGG caused extrinsic apoptosis through ROS generation that was AKT-dependent in breast cancer cells, without affecting primary mammary epithelial cells, suggesting potential cancer specificity of this natural compound. In addition, using HUVECs, AGG inhibited expression of the pro-angiogenic factor IGFBP-2 in an AKT-dependent manner, reducing angiogenic phenotypes both in vitro and in vivo. Overall, the present results establish that AGG promotes both apoptosis and anti-angiogenic activities in human breast tumor cells, which might be exploited for treatment of breast and other cancers.

摘要

相思子凝集素(AGG)是一种从相思子种子中分离出的植物凝集素,在小鼠模型中已证明具有抗肿瘤和免疫刺激作用。为了研究其对乳腺癌可能的抗肿瘤活性,我们在无胸腺裸鼠中建立了人乳腺肿瘤异种移植模型,并腹腔注射AGG。通过分别监测Ki-67和CD-31的表达证实,AGG抑制肿瘤生长和血管生成。此外,在用AGG处理的乳腺肿瘤中,TUNEL阳性细胞增加,这表明AGG通过诱导凋亡和抑制血管生成介导抗肿瘤活性。在分子水平上,AGG通过活性氧生成导致外源性凋亡,这在乳腺癌细胞中是AKT依赖性的,而不影响原代乳腺上皮细胞,表明这种天然化合物具有潜在的癌症特异性。此外,使用人脐静脉内皮细胞(HUVECs),AGG以AKT依赖性方式抑制促血管生成因子IGFBP-2的表达,在体外和体内均减少血管生成表型。总体而言,目前的结果表明,AGG在人乳腺肿瘤细胞中促进凋亡和抗血管生成活性,这可能被用于治疗乳腺癌和其他癌症。

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