Dipartimento di Farmacia-Scienze del Farmaco, Università degli Studi di Bari ALDO MORO, Via Orabona 4, 70125 Bari, Italy.
Molecules. 2021 Jun 19;26(12):3743. doi: 10.3390/molecules26123743.
Sigma-2 (σ) is an endoplasmic receptor identified as the Endoplasmic Reticulum (ER) transmembrane protein TMEM97. Despite its controversial identity, which was only recently solved, this protein has gained scientific interest because of its role in the proliferative status of cells; many tumor cells from different organs overexpress the σ receptor, and many σ ligands display cytotoxic actions in (resistant) cancer cells. These properties have shed light on the σ receptor as a potential druggable target to be bound/activated for the diagnosis or therapy of tumors. Additionally, diverse groups have shown how the σ receptor can be exploited for the targeted delivery of the anticancer drugs to tumors. As the cancer disease is a multifactorial pathology with multiple cell populations, a polypharmacological approach is very often needed. Instead of the simultaneous administration of different classes of drugs, the use of one molecule that interacts with diverse pharmacological targets, namely MultiTarget Directed Ligand (MTDL), is a promising and currently pursued strategy, that may overcome the pharmacokinetic problems associated with the administration of multiple molecules. This review aims to point out the progress regarding the σ ligands in the oncology field, with a focus on MTDLs directed towards σ receptors as promising weapons against (resistant) cancer diseases.
Sigma-2(σ)是一种内质网受体,被鉴定为内质网(ER)跨膜蛋白 TMEM97。尽管其身份颇具争议,直到最近才得到解决,但由于其在细胞增殖状态中的作用,这种蛋白质引起了科学界的兴趣;许多来自不同器官的肿瘤细胞过度表达 σ 受体,许多 σ 配体在(耐药)癌细胞中显示出细胞毒性作用。这些特性使 σ 受体成为一个有潜力的可结合/激活的药物靶点,可用于肿瘤的诊断或治疗。此外,许多研究小组已经展示了如何利用 σ 受体将抗癌药物靶向递送到肿瘤中。由于癌症疾病是一种具有多种细胞群体的多因素病理学,通常需要采用多药理学方法。多药理学方法不是同时给予不同类别的药物,而是使用一种与多种药理学靶点相互作用的分子,即多靶标导向配体(MTDL),这是一种很有前途且正在研究的策略,可能克服与给予多种分子相关的药代动力学问题。本综述旨在指出 σ 配体在肿瘤学领域的进展,重点介绍针对 σ 受体的 MTDL,作为对抗(耐药)癌症疾病的有希望的武器。