Anticancer bioactive peptide suppresses human gastric cancer growth through modulation of apoptosis and the cell cycle

被引：72

作者：

Su, Liya ^{[1
,2
]}

Xu, Guihua ^{[2
]}

Shen, Jie ^{[2
]}

Tuo, Ya ^{[3
]}

Zhang, Xingguang ^{[4
]}

Jia, Shuqin ^{[2
]}

Chen, Zhong ^{[5
]}

Su, Xiulan ^{[1
,2
]}

机构：

[1] Capital Med Univ, Dept Cell Biol, Beijing, Peoples R China

[2] Inner Mongolia Med Coll, Clin Med Res Ctr, Hohhot, Inner Mongolia, Peoples R China

[3] Inner Mongolia Med Coll, Dept Prevent Med, Hohhot, Inner Mongolia, Peoples R China

[4] Affiliated Hosp, Inner Mongolia Med Coll, Lab Testing Ctr, Hohhot, Inner Mongolia, Peoples R China

[5] Natl Inst Deafness & Other Commun Disorders, Tumor Biol Sect, Head & Neck Surg Branch, NIH, Bethesda, MD USA

来源：

ONCOLOGY REPORTS | 2010年 / 23卷 / 01期

基金：

中国国家自然科学基金;

关键词：

bioactive peptide; gastric cancer; tumor growth; apoptosis; cell cycle; C-MYC; STEM-CELLS; EXPRESSION; BCL-2; CARCINOGENESIS; CARCINOMAS; MEMBRANE; THERAPY; MARKERS; BAX;

D O I：

10.3892/or_00000599

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 [肿瘤学];

摘要：

Anticancer bioactive peptide (ACBP) was extracted from goat spleens with immunization by human gastric cancer extracts. ACBP was biochemically purified and identified as similar to 8,000 Da peptide. Here we report that ACBP significantly inhibited the growth of human gastric cancer line BGC-823 in vitro in a dose-dependent manner. ACBP induced BGC-823 cell apoptosis was observed morphologically both by light microscopy and electronic microscopy; and ACBP-induced apoptosis and G(0)/G(1) cell cycle arrest were quantified by Annexin V-FITC/PI staining and flow cytometry. At the molecular level, ACBP induced p16(Ink4), p21(Waf1), p27(Kipl), and bax tumor suppressor and apoptotic gene expression, as well as inhibited cyclin D1, c-myc, and bcl-2 gene expression that promote tumorigenesis. In vivo, ACBP dramatically inhibited human gastric tumor growth in a xenograft model with no apparent cytotoxicity to host. Our study suggests that ACBP could be a powerful anticancer biological product through induction of cell apoptosis and cell cycle arrest.

引用

页码：3 / 9

页数：7

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