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首页> 外文期刊>International journal of applied mechanics >Mechanism of Anti-Cancer Activity of Curcumin on Androgen-Dependent and Androgen-Independent Prostate Cancer
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Mechanism of Anti-Cancer Activity of Curcumin on Androgen-Dependent and Androgen-Independent Prostate Cancer

机译:姜黄素依赖性和雄激素无关前列腺癌抗癌活性的机制

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摘要

Prostate cancer (PCa) is a heterogeneous disease and ranked as the second leading cause of cancer-related deaths in males worldwide. The global burden of PCa keeps rising regardless of the emerging cutting-edge technologies for treatment and drug designation. There are a number of treatment options which are effectively treating localised and androgen-dependent PCa (ADPC) through hormonal and surgery treatments. However, over time, these cancerous cells progress to androgen-independent PCa (AIPC) which continuously grow despite hormone depletion. At this particular stage, androgen depletion therapy (ADT) is no longer effective as these cancerous cells are rendered hormone-insensitive and capable of growing in the absence of androgen. AIPC is a lethal type of disease which leads to poor prognosis and is a major contributor to PCa death rates. A natural product-derived compound, curcumin has been identified as a pleiotropic compound which capable of influencing and modulating a diverse range of molecular targets and signalling pathways in order to exhibit its medicinal properties. Due to such multi-targeted behaviour, its benefits are paramount in combating a wide range of diseases including inflammation and cancer disease. Curcumin exhibits anti-cancer properties by suppressing cancer cells growth and survival, inflammation, invasion, cell proliferation as well as possesses the ability to induce apoptosis in malignant cells. In this review, we investigate the mechanism of curcumin by modulating multiple signalling pathways such as androgen receptor (AR) signalling, activating protein-1 (AP-1), phosphatidylinositol 3-kinases/the serine/threonine kinase (PI3K/Akt/mTOR), wingless (Wnt)/ss-catenin signalling, and molecular targets including nuclear factor kappa-B (NF-kappa B), B-cell lymphoma 2 (Bcl-2) and cyclin D1 which are implicated in the development and progression of both types of PCa, ADPC and AIPC. In addition, the role of microRNAs and clinical trials on the anti-cancer effects of curcumin in PCa patients were also reviewed.
机译:前列腺癌(PCA)是一种异质疾病,并作为全球男性中癌症相关死亡的第二个主要原因。无论出现的治疗和药物指定,全球PCA负担都会保持上升。存在许多治疗方案,通过激素和手术治疗有效地治疗局部和雄激素依赖性PCA(ADPC)。然而,随着时间的推移,尽管激素耗尽,这些癌细胞对雄激素无关的PCA(AIPC)持续增长。在这种特殊阶段,雄激素耗尽治疗(ADT)不再有效,因为这些癌细胞使激素不敏感并在没有雄激素的情况下生长。 AIPC是一种致命的疾病,导致预后差,是PCA死亡率的主要贡献者。已经鉴定了天然产物衍生的化合物,姜黄素被鉴定为能够影响和调节各种分子靶标和信号通路的抗磷酸化合物,以表现其药用特性。由于这种多目标行为,其益处是对抗各种疾病,包括炎症和癌症疾病的益处至关重要。姜黄素通过抑制癌细胞生长和存活,炎症,侵袭,细胞增殖以及具有诱导恶性细胞凋亡的能力来表现出抗癌性能。在该综述中,我们通过调节雄激素受体(AR)信号传导,活化蛋白-1(AP-1),磷脂酰肌醇3-激酶/丝氨酸/苏氨酸激酶(PI3K / AKT / MTOR)来研究姜黄素的机制),无翅(Wnt)/ ss-catenin信号传导,包括核因子Kappa-B(NF-κB),B细胞淋巴瘤2(BCL-2)和细胞周期蛋白D1的分子靶标,这涉及开发和进展两种类型的PCA,ADPC和AIPC。此外,还审查了MicroRNA和临床试验对PCA患者姜黄素抗癌作用的作用。

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