Plumbagin Inhibits Cadmium-Induced Interleukin-6/STAT3 Signaling in the Triple-Negative Breast Cancer Cell Line.

Titiwadee Titiwattanakarn, Rapeewan Settacomkul, Thitima Kasemsuk, Pornpun Vivithanaporn
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Abstract

Introduction: Plumbagin has been found to reduce proinflammatory cytokine expression in activated macrophages and carrageenan-induced paw edema. Cadmium triggers the release of interleukin-6 (IL-6), a key mediator of inflammation and carcinogenesis in many cell types. The effects of plumbagin on cadmium-induced inflammation in triple-negative breast cancer cells are unknown.

Method: We investigated the effects of plumbagin on cadmium-induced IL-6 expression and signal transducer and activator of transcription 3 (STAT3) activation in MDA-MB-231, a triple-negative breast cancer cell line, using real-time PCR, ELISA, and Western blotting.

Result: Non-cytotoxic concentrations of cadmium chloride at 1 and 10 μM upregulated the IL-6 mRNA expression after 3 h of exposure and increased the IL-6 release after 24 h. Plumbagin at 4 μM or more was toxic to cells after 24 h. Plumbagin at 1 μM co-treated with cadmium reduced the expression and secretion of IL-6. At 24-h post-exposure, plumbagin decreased the levels of phosphorylated STAT3 induced by cadmium.

Conclusion: Plumbagin inhibits cadmium-induced IL-6/STAT3 signaling in a triple-negative breast cancer cell and further in vivo studies are required to elucidate the potential use of plumbagin on cancer progression.

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Plumbagin 可抑制三阴性乳腺癌细胞系中镉诱导的白细胞介素-6/STAT3 信号转导
研究发现,白桦素可降低活化巨噬细胞中促炎细胞因子的表达,降低卡拉胶诱导的足跖水肿。镉触发白细胞介素-6 (IL-6)的释放,IL-6是许多细胞类型炎症和致癌的关键介质。白丹素对镉诱导的三阴性乳腺癌细胞炎症的影响尚不清楚。方法:采用实时荧光定量PCR、酶联免疫吸附和Western blotting等方法,研究白丹素对镉诱导的乳腺癌MDA-MB-231细胞IL-6表达和STAT3激活的影响。结果:浓度为1 μM和10 μM的氯化镉对细胞无细胞毒性作用,3 h后可上调IL-6 mRNA的表达,24 h后可增加IL-6的释放量。浓度为4 μM及以上的铅巴苷在24 h后对细胞有毒性作用,浓度为1 μM的铅巴苷与镉共处理可降低IL-6的表达和分泌。暴露24小时后,白桦素降低镉诱导的磷酸化STAT3水平。结论:白丹素在三阴性乳腺癌细胞中抑制镉诱导的IL-6/STAT3信号,需要进一步的体内研究来阐明白丹素在癌症进展中的潜在作用。
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来源期刊
CiteScore
2.80
自引率
0.00%
发文量
779
审稿时长
3 months
期刊介绍: Cancer is a very complex disease. While many aspects of carcinoge-nesis and oncogenesis are known, cancer control and prevention at the community level is however still in its infancy. Much more work needs to be done and many more steps need to be taken before effective strategies are developed. The multidisciplinary approaches and efforts to understand and control cancer in an effective and efficient manner, require highly trained scientists in all branches of the cancer sciences, from cellular and molecular aspects to patient care and palliation. The Asia Pacific Organization for Cancer Prevention (APOCP) and its official publication, the Asia Pacific Journal of Cancer Prevention (APJCP), have served the community of cancer scientists very well and intends to continue to serve in this capacity to the best of its abilities. One of the objectives of the APOCP is to provide all relevant and current scientific information on the whole spectrum of cancer sciences. They aim to do this by providing a forum for communication and propagation of original and innovative research findings that have relevance to understanding the etiology, progression, treatment, and survival of patients, through their journal. The APJCP with its distinguished, diverse, and Asia-wide team of editors, reviewers, and readers, ensure the highest standards of research communication within the cancer sciences community across Asia as well as globally. The APJCP publishes original research results under the following categories: -Epidemiology, detection and screening. -Cellular research and bio-markers. -Identification of bio-targets and agents with novel mechanisms of action. -Optimal clinical use of existing anti-cancer agents, including combination therapies. -Radiation and surgery. -Palliative care. -Patient adherence, quality of life, satisfaction. -Health economic evaluations.
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