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一项对临床前研究中六种作为潜在乳腺癌抑制剂的生物活性化合物的综述。

A review of six bioactive compounds from preclinical studies as potential breast cancer inhibitors.

作者信息

Rampogu Shailima, Al-Antari Mugahed A, Oh Tae Hwan, Shaik Baji

机构信息

Cachet Big Data Lab, Hyderabad, 500045, Telangana, India.

Department of Artificial Intelligence, College of Software & Convergence Technology, Daeyang AI Center, Sejong University, Seoul, 05006, Republic of Korea.

出版信息

Mol Biol Rep. 2025 Feb 5;52(1):203. doi: 10.1007/s11033-025-10300-0.

Abstract

Breast cancer is one of the predominant causes of mortality in women worldwide. Although therapeutics such as surgery, chemotherapy, hormonal therapy, and radiotherapy have been used, they are associated with adverse effects or multidrug resistance. The use of natural compounds is a promising strategy, owing to their abundance and medicinal value. This review focuses on six natural compounds, namely cinnamaldehyde, diosmin, taxifolin, phloretin, arctigenin, and eugenol, and details their mechanisms of breast cancer inhibition based on in vitro and in vivo studies. These compounds generally promote apoptosis and cell cycle arrest, hinder metastasis and invasion, and decrease tumor growth. This review reinforces the use of natural compounds as therapeutics for breast cancer from their preclinical studies. These compounds might be promising for drug development due to their abundance, high reliability, and safety.

摘要

乳腺癌是全球女性主要的死亡原因之一。尽管已经采用了手术、化疗、激素治疗和放疗等治疗方法,但它们会带来不良反应或多药耐药性。由于天然化合物丰富且具有药用价值,使用天然化合物是一种很有前景的策略。本综述重点关注六种天然化合物,即肉桂醛、地奥司明、花旗松素、根皮素、牛蒡子苷元和丁香酚,并根据体外和体内研究详细阐述它们抑制乳腺癌的机制。这些化合物通常会促进细胞凋亡和细胞周期停滞,阻碍转移和侵袭,并抑制肿瘤生长。本综述通过临床前研究强化了将天然化合物用作乳腺癌治疗药物的观点。由于这些化合物丰富、可靠性高且安全,它们在药物开发方面可能很有前景。

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