子宫内膜癌的分子药理干预:综述。

IF 5.1 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-08-27 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S524181
Wei Qin, Yazhou Qi, Qianwen Li, Bei Wang, Jingmiao Wang, Xueke Ge, Yanhong Li, Xinyue Zhang, Kuan Liu
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引用次数: 0

摘要

子宫内膜癌是女性生殖系统常见的恶性肿瘤,由于其分子亚型多样,发病率上升,临床处理复杂。本文综述了EC的分子机制,特别是Bcl-2家族在肿瘤进展中凋亡调节和雌激素受体信号传导中的作用。我们探索针对这些途径的药理学干预,包括BH3模拟物和选择性雌激素受体调节剂,它们显示出希望,但面临阻力和副作用等挑战。此外,我们强调了姜黄素、紫杉醇和灵芝多糖等天然化合物作为辅助治疗的潜力,在临床前研究和早期临床试验中证明了疗效。本综述旨在为EC的个性化治疗策略的发展提供见解,并确定在未来治疗中优化临床结果的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular Pharmacological Interventions for Endometrial Cancer: A Comprehensive Review.

Molecular Pharmacological Interventions for Endometrial Cancer: A Comprehensive Review.

Molecular Pharmacological Interventions for Endometrial Cancer: A Comprehensive Review.

Molecular Pharmacological Interventions for Endometrial Cancer: A Comprehensive Review.

Endometrial cancer, a common malignancy of the female reproductive system, has a rising incidence and complex clinical management due to its diverse molecular subtypes. This review examines the molecular mechanisms underlying EC, particularly the roles of the Bcl-2 family in apoptosis regulation and estrogen receptor signaling in tumor progression. We explore pharmacological interventions targeting these pathways, including BH3 mimetics and selective estrogen receptor modulators, which show promise but face challenges such as resistance and adverse effects. Additionally, we highlight the potential of natural compounds like curcumin, paclitaxel, and Ganoderma lucidum polysaccharides as adjunctive therapies, demonstrating efficacy in preclinical studies and early-phase clinical trials. This review aims to provide insights into the development of personalized therapeutic strategies for EC and to identify opportunities for optimizing clinical outcomes in future treatments.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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