Two-in-One Polymeric NO-Donor Prodrugs Mediate Precision and Synergistic Prostate Cancer Treatment.
Bingbing ZhaoYuqing WanXiang ZhouJunmei ZhangJiaxin ChenJiachen YangYunzhu LiuWei ChenYinan ZhongHongliang QianPublished in: ACS applied materials & interfaces (2023)
Chemotherapy predominates in clinical treatment of prostate cancer (PCa), while irreversible resistance to chemotherapeutics and severe side effects hinder the therapeutic efficacy, especially in castration-resistant PCa (CRPC). Herein, a bombesin (BBN)-decorated two-in-one prodrug (T-NO/E 2 -PMs) incorporating a polymeric nitric oxide (NO) donor and acetal-linked 17β-estradiol (E 2 ) in one backbone is developed, aiming to inhibit androgen receptor (AR) expression, reprogram the tumor microenvironment of CRPC, and enhance estradiol-mediated hypoxic CRPC therapy. Following efficient internalization mediated by BBN, T-NO/E 2 -PMs releases estradiol and NO in response to the unique intracellular environments. Both in vitro and in vivo studies demonstrate that the T-NO/E 2 -PMs nano-prodrug along with NO release potently downregulates AR levels to reverse CRPC and further enhances the chemo-sensitization of estradiol to PCa PC-3 cell apoptosis and the inhibition of metastasis. Collectively, this two-in-one nano-prodrug strategy offers a promising platform for construction of advanced nanomedicine to boost the therapeutic efficacy.
Keyphrases
- cancer therapy
- prostate cancer
- drug delivery
- estrogen receptor
- drug release
- nitric oxide
- radical prostatectomy
- poor prognosis
- cell proliferation
- squamous cell carcinoma
- radiation therapy
- mesenchymal stem cells
- photodynamic therapy
- reactive oxygen species
- case control
- single cell
- replacement therapy
- long non coding rna
- nitric oxide synthase
- bone marrow
- drug induced