CD151基因表达下调可降低雌激素受体阳性乳腺癌细胞的存活率

Gayatri Devi, A. Badana, M. Ch, P. Muralimohan, Shail, Rakhi P. Naik, I. BhaskarReddy, Seema Kumari, R. Malla
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引用次数: 4

摘要

Tetraspnin CD151参与增殖、运动和侵袭。然而,CD151在雌激素受体阳性乳腺癌中的作用尚未报道。在本研究中,我们报道了CD151在ER阳性细胞系及其潜在分子伴侣存活中的作用。将CD151 shRNA表达载体转染MCF-7细胞,采用RT-PCR方法评价其表达效果。MCF-7细胞的增殖、迁移、侵袭、细胞粘附和血管生成能力被CD151特异性shRNA敲除。将细胞周期阻滞在G2/M期,诱导细胞凋亡。敲低CD151可降低c-myc、α3β1整合素、IL-8、Ras、FAK、VEGF的表达。结果表明,CD151基因沉默影响其网络伴侣的表达,与MCF-7细胞存活相关。因此,CD151可能是管腔和基底亚型的潜在靶点。
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Knockdown of CD151 Gene Expression Reduces Survival of Estrogen Receptor Positive Breast Cancer Cells
Tetraspnin CD151 is involved in proliferation, motility, and invasion. Yet, the role of CD151 in estrogen receptor positive breast cancer is not reported. In the present study, the role of CD151 in survival of ER positive cell line and the underlying molecular partners was reported. CD151 shRNA expression vector was transfected into MCF-7 cells and its efficacy was evaluated by RT-PCR. The capacity of proliferation, migration, and invasion, cell adhesion, angiogenesis of MCF-7 cells was diminished by the knockdown of CD151 via CD151 specific shRNA. It arrested the cell cycle at G2/M phase and induced the apoptosis. The expressions of c-myc, α3β1 integrin, IL-8, Ras, FAK and VEGF were reduced by knockdown of CD151. The results conclude that CD151 gene silencing affects the expression of its network partner’s associate with survival of MCF-7 cells. Therefore, CD151 may be a potential target of luminal and basal subtypes.
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