Alpha mangostin inhibits proliferation, migration, and invasion of human breast cancer cells via STAT3 inhibition

IF 2 Q3 ONCOLOGY
Lakshmi Vineela Nalla , Anil Dharavath , Santosh Kumar Behera , Amit Khairnar
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引用次数: 2

Abstract

Background

Signal Transducer and Activator of Transcription 3 (STAT3) is an identified critical protein associated with the progression of cancer. Alpha mangostin (α-M), a powerful dietary xanthone found to have anti-cancer properties against various cancers. However, the precise mechanism of its anti-cancer activity is not fully understood. Therefore, the current work hypothesized that targeting STAT3 with α-M inhibits the migration, invasion, and proliferation of breast cancer cells. Firstly, we evaluated the binding affinity of α-M/STAT3 complex using molecular dynamic simulations (MDS) and further we determined the likely underlying mechanism of STAT3 through in-vitro experiments. α-M treatment affected the levels of STAT3 phosphorylation, hnRNP-A1, PKM2, and EMT markers. α-M stimulation in breast cancer cells also resulted in suppressed migratory and invasive behaviour. More importantly, the treatment also affected the Ki67 and BrdU positive cells. In summary, we found the anti-migratory and anti-proliferative actions of α-M in breast cancer cells via STAT3 inhibition. Also, the study significantly adds a new nutraceutical for therapeutic intervention of invasive breast cancer.

Abstract Image

α-芒果苷通过抑制STAT3抑制人乳腺癌症细胞的增殖、迁移和侵袭
信号转导和转录激活因子3 (STAT3)是一种与癌症进展相关的关键蛋白。α山竹素(α-M),一种强大的膳食山酮,被发现对各种癌症具有抗癌特性。然而,其抗癌活性的确切机制尚不完全清楚。因此,目前的研究假设用α-M靶向STAT3可以抑制乳腺癌细胞的迁移、侵袭和增殖。首先,我们通过分子动力学模拟(MDS)评估α-M/STAT3复合物的结合亲和力,并进一步通过体外实验确定STAT3可能的潜在机制。α-M处理影响STAT3磷酸化、hnRNP-A1、PKM2和EMT标志物水平。α-M对乳腺癌细胞的刺激也抑制了癌细胞的迁移和侵袭行为。更重要的是,治疗也影响了Ki67和BrdU阳性细胞。综上所述,我们发现α-M通过抑制STAT3在乳腺癌细胞中的抗迁移和抗增殖作用。同时,本研究为浸润性乳腺癌的治疗干预增加了一种新的营养品。
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来源期刊
Advances in cancer biology - metastasis
Advances in cancer biology - metastasis Cancer Research, Oncology
CiteScore
2.40
自引率
0.00%
发文量
0
审稿时长
103 days
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