Glucocorticoid Receptor-Mediated Engineered Cancer Stem Cell-Led Therapy and Inhibition of Recurrence in Colorectal Cancer

IF 4.9 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Molecular Pharmaceutics Pub Date : 2026-10-05 Epub Date: 2026-09-16 DOI:10.1021/acs.molpharmaceut.6c00889
Pritam Das, Tithi Bhattacharyya, Susmitha Vangala, Keerthana Murthati, Soumyadeep Poddar, Anjaneyulu Eanti, Rajkumar Banerjee
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引用次数: 0

Abstract

Dysregulated wnt/β-catenin signaling cascades drive self-renewal, proliferation, differentiation, and therapeutic resistance in cancer stem cells (CSCs), thus contributing to their tumor aggression and poor clinical outcomes. Earlier, we demonstrated that a glucocorticoid receptor (GR)-targeted liposomal formulation carrying dexamethasone (Dex) and the wnt/β-catenin inhibitor FH535 (D1XFH) selectively sensitizes colorectal cancer (CRC) cells and suppresses tumor growth. Herein, we investigate the immuno-therapeutic potential of D1XFH, especially within colorectal CSCs and against tumor recurrence. Our results reveal that D1XFH significantly downregulates CD133 and stemness-associated transcription factors Nanog, Sox2, and Oct4 in CSCs. D1XFH induces selective cytotoxicity by enhancing ROS generation, triggering apoptosis, reducing clonogenic potential, inhibiting cellular migration, and reversing multidrug resistance in CSCs. Co-administration of D1XFH-engineered CSCs and D1XFH into subcutaneous tumor-bearing mice resulted in pronounced tumor regression, accompanied by inhibition of wnt/β-catenin signaling, reversal of EMT, and antitumorigenic immune responses, while improving long-term survival. Additionally, D1XFH treatments post-tumor resection resulted in near-zero tumor recurrence, while zero recurrence was observed even after tumor re-challenge. We observed 250 day long-term survivability with possible resurgence of immune-memory response within tumor-resected, D1XFH-treated mice. Collectively, dual targeting of GR and wnt/β-catenin-driven CSC engineering and immunomodulation is a promising strategy for colorectal cancer therapy.

糖皮质激素受体介导的工程化肿瘤干细胞主导治疗和抑制结直肠癌复发
失调的wnt/β-catenin信号级联驱动癌症干细胞(CSCs)的自我更新、增殖、分化和治疗抗性,从而导致其肿瘤侵袭性和不良的临床结果。先前,我们证明了糖皮质激素受体(GR)靶向脂质体制剂携带地塞米松(Dex)和wnt/β-catenin抑制剂FH535 (D1XFH)选择性致敏结直肠癌(CRC)细胞并抑制肿瘤生长。在此,我们研究了D1XFH的免疫治疗潜力,特别是在结直肠csc和肿瘤复发。我们的研究结果显示,D1XFH在CSCs中显著下调CD133和干细胞相关转录因子Nanog、Sox2和Oct4。D1XFH通过增强ROS生成、触发细胞凋亡、降低克隆生成潜能、抑制细胞迁移和逆转CSCs的多药耐药,诱导选择性细胞毒性。将D1XFH工程的CSCs和D1XFH联合应用于皮下荷瘤小鼠,可导致明显的肿瘤消退,同时抑制wnt/β-catenin信号,逆转EMT和抗肿瘤免疫反应,同时提高长期生存率。此外,D1XFH治疗肿瘤切除后的肿瘤几乎为零复发,即使在肿瘤再次攻击后也观察到零复发。我们在切除肿瘤的d1xfh治疗小鼠中观察了250天的长期存活率,并可能重新出现免疫记忆反应。总之,GR和wnt/β-catenin驱动的CSC工程和免疫调节的双重靶向是一种很有前途的结直肠癌治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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