Neem leaf extract inhibits mammary carcinogenesis by altering cell proliferation, apoptosis, and angiogenesis

被引:36
作者
Arumugam, Arunkumar [1 ]
Agullo, Pamela [1 ]
Boopalan, Thiyagarajan [1 ]
Nandy, Sushmita [1 ]
Lopez, Rebecca [1 ]
Gutierrez, Christina [1 ]
Narayan, Mahesh [2 ]
Rajkumar, Lakshmanaswamy [1 ]
机构
[1] Texas Tech Univ Hlth Sci Ctr, Dept Biomed Sci, Ctr Excellence Canc Res, Paul L Foster Sch Med, El Paso, TX USA
[2] Univ Texas El Paso, Dept Chem, El Paso, TX 79968 USA
关键词
Neem; breast cancer; apoptosis; cell cycle; angiogenesis; BREAST-CANCER CELLS; HORMONAL PROMOTION; CYCLIN D1B; IN-VITRO; EXPRESSION; P53; CHEMOPREVENTION; ANGIOPOIETIN-1; COMPLEMENTARY; AMPLIFICATION;
D O I
10.4161/cbt.26604
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Plant-based medicines are useful in the treatment of cancer. Many breast cancer patients use complementary and alternative medicine in parallel with conventional treatments. Neem is historically well known in Asia and Africa as a versatile medicinal plant with a wide spectrum of biological activities. The experiments reported herein determined whether the administration of an ethanolic fraction of Neem leaf (EFNL) inhibits progression of chemical carcinogen-induced mammary tumorigenesis in rat models. Seven-week-old female Sprague Dawley rats were given a single intraperitoneal injection of N-methyl-N-nitrosourea (MNU). Upon the appearance of palpable mammary tumors, the rats were divided into vehicle-treated control groups and EFNL-treated groups. Treatment with EFNL inhibited MNU-induced mammary tumor progression. EFNL treatment was also highly effective in reducing mammary tumor burden and in suppressing mammary tumor progression even after the cessation of treatment. Further, we found that EFNL treatment effectively upregulated proapoptotic genes and proteins such as p53, B cell lymphoma-2 protein (Bcl-2)-associated X protein (Bax), Bcl-2-associated death promoter protein (Bad) caspases, phosphatase and tensin homolog gene (PTEN), and c-Jun N-terminal kinase (JNK). In contrast, EFNL treatment caused downregulation of anti-apoptotic (Bcl-2), angiogenic proteins (angiopoietin and vascular endothelial growth factor A [VEGF-A]), cell cycle regulatory proteins (cyclin D1, cyclin-dependent kinase 2 [Cdk2], and Cdk4), and pro-survival signals such as NFB, mitogen-activated protein kinase 1 (MAPK1). The data obtained in this study demonstrate that EFNL exert a potent anticancer effect against mammary tumorigenesis by altering key signaling pathways.
引用
收藏
页码:26 / 34
页数:9
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