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组合化化疗敏纳米医学方法治疗乳腺癌。

Combinatorial Chemosensitive Nanomedicine Approach for the Treatment of Breast Cancer.

机构信息

Department of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi - 110062, India.

Department of Pharmacy, National University of Singapore, Singapore 117559, Singapore.

出版信息

Curr Mol Med. 2023;23(9):876-888. doi: 10.2174/1566524023666220819122948.

Abstract

Breast cancer is the most commonly diagnosed type of cancer and ranks second among cancer that leads to death. From becoming the foremost reason for global concern, this multifactorial disease is being treated by conventional chemotherapies that are associated with severe side effects, with chemoresistance being the ruling reason. Exemestane, an aromatase inhibitor that has been approved by the US FDA for the treatment of breast cancer in post-menopausal women, acts by inhibiting the aromatase enzyme, in turn, inhibiting the production of estrogen. However, the clinical application of exemestane remains limited due to its poor aqueous solubility and low oral bioavailability. Furthermore, the treatment regimen of exemestane often leads to thinning of bone mineral density. Thymoquinone, a natural compound derived from the oil of the seeds of Nigella sativa Linn, possesses the dual property of being a chemosensitizer and chemotherapeutic agent. In addition, it has been found to exhibit potent bone protection properties, as evidenced by several studies. To mitigate the limitations associated with exemestane and to deliver to the cancerous cells overcoming chemoresistance, the present hypothesis has been put forth, wherein a natural chemosensitizer and chemotherapeutic agent thymoquinone will be incorporated into a lipid nanocarrier along with exemestane for combinatorial delivery to cancer cells. Additionally, thymoquinone being bone protecting will help in ousting the untoward effect of exemestane at the same time delivering it to the required malignant cells, safeguarding the healthy cells, reducing the offsite toxicity, and providing potent synergistic action.

摘要

乳腺癌是最常见的癌症类型,也是癌症死亡的第二大原因。这种多因素疾病已成为全球首要关注的问题,目前采用的常规化疗方法虽然有效,但副作用严重,而且还会导致耐药性。依西美坦是一种芳香酶抑制剂,已被美国 FDA 批准用于治疗绝经后妇女的乳腺癌,它通过抑制芳香酶来抑制雌激素的产生。然而,由于其水溶性差和口服生物利用度低,依西美坦的临床应用仍然受到限制。此外,依西美坦的治疗方案常常导致骨密度降低。姜黄素是从黑种草子油中提取的一种天然化合物,具有化疗增敏剂和化疗药物的双重特性。此外,已有多项研究表明,它具有很强的骨保护作用。为了克服依西美坦的局限性,并为癌细胞提供克服耐药性的治疗方法,本研究提出了一个假设,即将天然化疗增敏剂和化疗药物姜黄素与依西美坦一起包载于脂质纳米载体中,用于联合递送至癌细胞。此外,姜黄素具有保护骨骼的作用,因此可以消除依西美坦的不良作用,同时将其递送至所需的恶性细胞,保护健康细胞,降低场外毒性,并提供有效的协同作用。

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