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在多发性骨髓瘤患者中,对 RD 治疗的深度血液学反应与 CD138+浆细胞中 IL-17R 的过度表达有关。

Deep hematologic response to RD treatment in patients with multiple myeloma is associated with overexpression of IL-17R in CD138+ plasma cells.

机构信息

Department of General Pathology, Pomeranian Medical University, 70-111, Szczecin, Poland.

Pharmaceutical Facility of Pomeranian Medical University, 71-899, Szczecin, Poland.

出版信息

Sci Rep. 2024 Oct 9;14(1):23559. doi: 10.1038/s41598-024-74558-3.

Abstract

Lenalidomide (LEN) is widely used immunomodulatory drug (IMiD). Nonetheless, despite its efficacy, over time patients become resistant to LEN and relapse. Due to high clinical relevance, drug resistance in MM is being thoroughly investigated. However, less is known about predictors of good response to LEN-based treatment. The aim of this study was to identify molecular pathways associated with good and long response to LEN. The study included newly diagnosed MM patients (NDMM) and MM patients treated with first-line LEN and dexamethasone (RD) who achieved and least very good partial remission (VGPR). RNA was isolated from MM cells and new-generation sequencing was performed. Obtained results were validated with qRT-PCR. A global increase in gene expression was found in the RD group compared to NDMM, suggesting the involvement of epigenetic mechanisms. Moreover, upregulation of genes controlling the interaction within MM niche was detected. Next, genes controlling immune response were upregulated. In particular, the gene encoding the IL-17 receptor was overexpressed in the RD group which is a novel finding. This should be emphasized because IL-17-related signaling can potentially be targeted, providing the rationale for future research. Establishing the molecular background associated with long-lasting and profound response to LEN may improve LEN-based chemotherapy regimens and facilitate the development of adjuvant therapies to enhance its anti-MM activity.

摘要

来那度胺(LEN)是一种广泛应用的免疫调节药物(IMiD)。尽管其疗效显著,但随着时间的推移,患者会对 LEN 产生耐药性并复发。鉴于其重要的临床意义,目前正在对 MM 中的耐药性进行深入研究。然而,对于预测对 LEN 为基础的治疗反应良好的因素,我们知之甚少。本研究旨在确定与 LEN 良好和长期反应相关的分子途径。该研究纳入了新诊断的多发性骨髓瘤(NDMM)患者和接受一线 LEN 和地塞米松(RD)治疗并获得至少非常好的部分缓解(VGPR)的 MM 患者。从 MM 细胞中分离 RNA,并进行新一代测序。使用 qRT-PCR 验证获得的结果。与 NDMM 相比,RD 组中发现了基因表达的整体增加,这表明涉及表观遗传机制。此外,还检测到控制 MM 龛内相互作用的基因上调。接下来,控制免疫反应的基因被上调。特别是,RD 组中编码白细胞介素 17 受体的基因过度表达,这是一个新的发现。这一点值得强调,因为 IL-17 相关信号通路可能成为潜在的治疗靶点,为未来的研究提供了依据。确定与 LEN 持久和深度反应相关的分子背景,可能会改善基于 LEN 的化疗方案,并促进辅助治疗的发展,以增强其抗 MM 活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3a5/11464892/4a8c63310c44/41598_2024_74558_Fig1_HTML.jpg

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