PI3K/AKT/mTOR Inhibitor Drug Candidates for the Treatment of Hormone Resistant Breast Cancer: A Systematic Review

Lucas Bernardim de Oliveira, Bárbara Mendes Paz Chao, A. Bini, M. Cordeiro, Emerson Carraro
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Abstract

Breast cancer is the second most diagnosed type of cancer in women, with approximately 2.3 million cases reported in 2020. According to estimates by Brazil's National Cancer Institute, there will be approximately 74,000 new cases in the three-year period 2023-2025. It is divided into 4 molecular subtypes, Luminal A, Luminal B (hormone-positive), HER-2 and triple-negative. Regarding treatment, particularly for the luminal subtypes, hormone therapy is fundamental, since they grow from estrogen stimulation. However, processes can occur that lead to therapeutic resistance, such as mutations in the PI3K/AKT/mTOR pathway, which acts in the regulation of various cellular functions. The search for drugs that inhibit this pathway as an alternative treatment may play a key role in overcoming this resistance. This systematic review aimed to study new candidate drugs for inhibiting the PI3K/AKT/mTOR pathway as an alternative treatment in cases of resistance to hormone therapy. The study was conducted in accordance with the PRISMA guidelines, using the PubMed database with the following terms: "breast cancer", "PI3K/AKT/mTOR", "immunotherapy" without restriction of year and language. A total of 36 articles were found and 3 were included in this review. The drug candidates presented promising results in terms of inhibiting the PI3K/AKT/mTOR pathway, as well as some advantages such as a reduction in adverse effects, an increase in the average density of cytotoxic T cells and greater expression of interferon signaling genes, which through their immunoregulatory function lead to an increase in the body's ability to react to tumor cells. Despite this, there is still a need for more studies on the subject, especially in vivo studies that can assess the biosafety and efficacy profile, with the aim of compiling sufficient data to make the introduction of these new drugs in breast cancer therapy a reality.
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治疗激素耐药乳腺癌的 PI3K/AKT/mTOR 抑制剂候选药物:系统综述
乳腺癌是女性诊断出的第二大癌症类型,2020 年报告的病例约为 230 万例。根据巴西国家癌症研究所的估计,2023-2025 年三年内将新增约 74,000 例病例。乳腺癌分为 4 个分子亚型,分别是 A 型、B 型(激素阳性)、HER-2 和三阴性。在治疗方面,尤其是对于管腔亚型,激素治疗是基础,因为它们是在雌激素刺激下生长的。然而,可能会出现导致耐药性的过程,如 PI3K/AKT/mTOR 通路的突变,该通路在调节各种细胞功能方面发挥作用。寻找抑制该通路的药物作为替代治疗方法,可能会在克服耐药性方面发挥关键作用。本系统综述旨在研究抑制 PI3K/AKT/mTOR 通路的新候选药物,作为激素治疗耐药病例的替代治疗方法。研究按照 PRISMA 指南进行,使用 PubMed 数据库中的以下术语:"乳腺癌"、"PI3K/AKT/mTOR"、"免疫疗法",不限年份和语言。共找到 36 篇文章,其中 3 篇被纳入本综述。候选药物在抑制PI3K/AKT/mTOR通路方面取得了可喜的成果,同时还具有一些优势,如减少不良反应、增加细胞毒性T细胞的平均密度、增加干扰素信号基因的表达等,这些基因通过其免疫调节功能提高了机体对肿瘤细胞的反应能力。尽管如此,我们仍然需要对这一主题进行更多的研究,特别是可以评估生物安全性和疗效的体内研究,目的是收集足够的数据,使这些新药在乳腺癌治疗中的应用成为现实。
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