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蛋白酶激活受体F2R是卵巢癌患者新的诊断/预后及治疗应用的潜在靶点。

Protease-Activated Receptor F2R Is a Potential Target for New Diagnostic/Prognostic and Treatment Applications for Patients with Ovarian Cancer.

作者信息

Khetan Riya, Lokman Noor A, Eldi Preethi, Price Zoe K, Oehler Martin K, Brooks Doug A, Blencowe Anton, Garg Sanjay, Ricciardelli Carmela, Albrecht Hugo

机构信息

Centre of Pharmaceutical Innovation, UniSA Clinical and Health Sciences, University of South Australia, Adelaide, SA 5000, Australia.

Discipline of Obstetrics and Gynaecology, Adelaide Medical School, Robinson Research Institute, University of Adelaide, Adelaide, SA 5000, Australia.

出版信息

Int J Mol Sci. 2025 Sep 2;26(17):8529. doi: 10.3390/ijms26178529.

Abstract

Effective treatment of ovarian cancer is limited by late-stage detection and chemotherapy resistance. There is a clinical need for the discovery of novel molecular targets to enable the development of innovative theranostic approaches. We investigated the coagulation factor II receptor/protease-activated receptor 1 (F2R/PAR1) as a potential diagnostic/prognostic biomarker and therapeutic target for ovarian cancer treatment. Public RNA sequence and DNA microarray data were used to analyze F2R gene expression in ovarian cancers, with protein expression confirmed in tumor samples by flow cytometry, immunofluorescence, and immunohistochemistry (IHC). Functional assays were conducted to study effects of F2R suppression on tumor progression. Our analysis confirmed elevated F2R mRNA and protein expression in ovarian cancers, notably in patients with metastatic and chemotherapy-resistant disease. Kaplan-Meier survival analysis demonstrated an association between high F2R protein detection and reduced progression-free survival. F2R suppression in ovarian cancer cell lines reduced tumor cell motility, invasion, spheroid formation, and metabolism and enhanced carboplatin sensitivity. F2R is a compelling diagnostic/prognostic and therapeutic target that could be used to treat chemotherapy-resistant and metastatic disease. The evaluation of novel F2R targeting strategies, using antibody-conjugated drugs or F2R ligand-decorated drug carriers, could lead to the development of effective therapeutics for patients with ovarian cancer.

摘要

卵巢癌的有效治疗受到晚期检测和化疗耐药性的限制。临床上需要发现新的分子靶点,以推动创新的治疗诊断方法的发展。我们研究了凝血因子II受体/蛋白酶激活受体1(F2R/PAR1)作为卵巢癌治疗的潜在诊断/预后生物标志物和治疗靶点。利用公开的RNA序列和DNA微阵列数据来分析卵巢癌中F2R基因的表达,并通过流式细胞术、免疫荧光和免疫组织化学(IHC)在肿瘤样本中证实蛋白表达。进行功能试验以研究F2R抑制对肿瘤进展的影响。我们的分析证实卵巢癌中F2R mRNA和蛋白表达升高,特别是在转移性和化疗耐药性疾病患者中。Kaplan-Meier生存分析表明,高F2R蛋白检测与无进展生存期缩短之间存在关联。卵巢癌细胞系中F2R的抑制降低了肿瘤细胞的运动性、侵袭性、球体形成和代谢,并增强了卡铂敏感性。F2R是一个有吸引力的诊断/预后和治疗靶点,可用于治疗化疗耐药性和转移性疾病。使用抗体偶联药物或F2R配体修饰的药物载体对新型F2R靶向策略进行评估,可能会为卵巢癌患者开发出有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798f/12428987/e5b39752af70/ijms-26-08529-g001.jpg

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