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针对乳腺癌亚型中癌症干细胞的新治疗策略的临床前和临床试验。

Preclinical and Clinical Trials of New Treatment Strategies Targeting Cancer Stem Cells in Subtypes of Breast Cancer.

机构信息

Unidad de Innovación en Prevención y Oncología de Precisión, Centro Oncológico, Facultad de Medicina, Universidad Católica del Maule, Talca 3480094, Chile.

In Vivo Tumor Biology Research Facility, Centro Oncológico, Facultad de Medicina, Universidad Católica del Maule, Talca 3480094, Chile.

出版信息

Cells. 2023 Feb 24;12(5):720. doi: 10.3390/cells12050720.

Abstract

Breast cancer (BC) can be classified into various histological subtypes, each associated with different prognoses and treatment options, including surgery, radiation, chemotherapy, and endocrine therapy. Despite advances in this area, many patients still face treatment failure, the risk of metastasis, and disease recurrence, which can ultimately lead to death. Mammary tumors, like other solid tumors, contain a population of small cells known as cancer stem-like cells (CSCs) that have high tumorigenic potential and are involved in cancer initiation, progression, metastasis, tumor recurrence, and resistance to therapy. Therefore, designing therapies specifically targeting at CSCs could help to control the growth of this cell population, leading to increased survival rates for BC patients. In this review, we discuss the characteristics of CSCs, their surface biomarkers, and the active signaling pathways associated with the acquisition of stemness in BC. We also cover preclinical and clinical studies that focus on evaluating new therapy systems targeted at CSCs in BC through various combinations of treatments, targeted delivery systems, and potential new drugs that inhibit the properties that allow these cells to survive and proliferate.

摘要

乳腺癌 (BC) 可以分为多种组织学亚型,每种亚型都与不同的预后和治疗选择相关,包括手术、放疗、化疗和内分泌治疗。尽管在这一领域取得了进展,但许多患者仍面临治疗失败、转移风险和疾病复发的风险,最终导致死亡。乳腺肿瘤与其他实体肿瘤一样,含有一群称为癌症干细胞样细胞 (CSC) 的小细胞,这些细胞具有高肿瘤形成潜力,并参与癌症的起始、进展、转移、肿瘤复发以及对治疗的耐药性。因此,设计专门针对 CSC 的治疗方法可能有助于控制这些细胞群体的生长,从而提高 BC 患者的生存率。在这篇综述中,我们讨论了 CSC 的特征、它们的表面生物标志物以及与 BC 中干性获得相关的活跃信号通路。我们还介绍了专注于通过各种治疗组合、靶向递送系统以及抑制这些细胞生存和增殖能力的潜在新药来评估针对 BC 中 CSC 的新治疗系统的临床前和临床研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/10001180/e0113c84f442/cells-12-00720-g001.jpg

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