Role of Fyn expression in predicting the sensitivity to platinum‑based chemotherapy in patients with ovarian serous carcinoma.

IF 2.5 4区 医学 Q3 ONCOLOGY
Eijiro Uchikura,Takeshi Fukuda,Tomoki Sengiku,Takuya Noda,Yuichiro Awazu,Takuma Wada,Reiko Tasaka,Makoto Yamauchi,Tomoyo Yasui,Toshiyuki Sumi
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引用次数: 0

Abstract

Ovarian serous carcinoma is a gynecological malignancy associated with a high mortality rate, which is commonly diagnosed in the first instance at a late stage and has a propensity to develop resistance to platinum-based chemotherapy. Identifying reliable biomarkers for platinum sensitivity is critical for improving patient outcomes. The present retrospective study included 64 patients with high-grade serous ovarian carcinoma (Federation of Gynecology and Obstetrics stages III or IV). Patients were classified as platinum-sensitive (no relapse within 6 months of the last platinum administration) or platinum-resistant (relapse within 6 months). Immunohistochemical analysis was performed to evaluate Fyn expression in tumor tissues, and Fyn knockdown experiments were performed using the OVSAHO ovarian cancer cell line to assess carboplatin sensitivity. Fyn expression was significantly higher in platinum-resistant patients compared with in platinum-sensitive patients (P<0.01). A weighted Fyn expression score was developed and a cutoff score of 6 was determined to predict platinum sensitivity with a specificity of 65.5% and a sensitivity of 62.9%. Patients with low Fyn expression (score ≤6) exhibited higher platinum sensitivity and longer overall survival (P<0.05). Multivariate analysis identified Fyn expression and postoperative residual tumor size as independent predictors of platinum sensitivity (P=0.033 and P=0.023, respectively). In vitro, Fyn knockdown significantly increased carboplatin sensitivity in ovarian cancer cells (P<0.05). Fyn, a member of the Src family of kinases, serves a crucial role in various cellular functions and has been implicated in chemotherapy resistance. The results demonstrated a notable association between Fyn expression and platinum sensitivity in ovarian serous carcinoma. The findings suggested that Fyn may serve as a predictive biomarker for response to platinum-based chemotherapy, offering the potential for more personalized treatment strategies. To the best of our knowledge, the present study is the first to establish an association between Fyn expression and platinum sensitivity in advanced ovarian serous carcinoma. Prospective studies with larger, multi-center cohorts and comprehensive biomarker analyses are recommended to validate and extend these results, ultimately improving therapeutic strategies and patient prognosis.
Fyn 表达在预测卵巢浆液性癌患者对铂类化疗敏感性中的作用。
卵巢浆液性癌是一种死亡率很高的妇科恶性肿瘤,通常在晚期才被确诊,而且容易对铂类化疗产生耐药性。确定铂敏感性的可靠生物标志物对于改善患者预后至关重要。本回顾性研究纳入了64名高级别浆液性卵巢癌(妇产科联盟III期或IV期)患者。患者被分为铂敏感型(最后一次使用铂后6个月内未复发)和铂耐药型(6个月内复发)。免疫组化分析评估了肿瘤组织中Fyn的表达,并使用OVSAHO卵巢癌细胞系进行了Fyn基因敲除实验,以评估卡铂的敏感性。与铂敏感患者相比,铂耐药患者的 Fyn 表达明显升高(P<0.01)。研究人员制定了一个加权 Fyn 表达评分,并确定以 6 分为临界值来预测铂敏感性,其特异性为 65.5%,敏感性为 62.9%。低Fyn表达(评分≤6)的患者具有更高的铂敏感性和更长的总生存期(P<0.05)。多变量分析发现,Fyn表达和术后残留肿瘤大小是铂敏感性的独立预测因素(分别为P=0.033和P=0.023)。在体外,Fyn基因敲除可显著增加卵巢癌细胞对卡铂的敏感性(P<0.05)。Fyn是Src激酶家族的成员,在多种细胞功能中发挥着重要作用,并与化疗耐药性有关。研究结果表明,Fyn的表达与卵巢浆液性癌对铂类药物的敏感性有明显的关联。研究结果表明,Fyn可作为铂类化疗反应的预测性生物标志物,为更个性化的治疗策略提供了可能性。据我们所知,本研究是首次在晚期卵巢浆液性癌中建立 Fyn 表达与铂敏感性之间的联系。我们建议进行更大规模的多中心队列前瞻性研究和全面的生物标志物分析,以验证和扩展这些结果,最终改善治疗策略和患者预后。
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
Oncology Letters
Oncology Letters ONCOLOGY-
CiteScore
5.70
自引率
0.00%
发文量
412
审稿时长
2.0 months
期刊介绍: Oncology Letters is a monthly, peer-reviewed journal, available in print and online, that focuses on all aspects of clinical oncology, as well as in vitro and in vivo experimental model systems relevant to the mechanisms of disease. The principal aim of Oncology Letters is to provide the prompt publication of original studies of high quality that pertain to clinical oncology, chemotherapy, oncogenes, carcinogenesis, metastasis, epidemiology and viral oncology in the form of original research, reviews and case reports.
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