College of Creative Studies, Niigata University, 8050 Ikarashi-nino-cho, Nishi-ku, Niigata 950-2181, Japan.
College of Creative Studies, Niigata University, 8050 Ikarashi-nino-cho, Nishi-ku, Niigata 950-2181, Japan.
Pathol Res Pract. 2021 Nov;227:153621. doi: 10.1016/j.prp.2021.153621. Epub 2021 Sep 17.
Numerous studies have examined the prognostic value of ubiquitin-specific protease 7 (USP7) in cancer, but the results remain controversial. Differences in assessment assays (mRNA/protein) used could be a potential confounding factor. Thus, we extracted studies that measured the protein expression and performed a meta-analysis to assess the prognostic role of USP7 expression in cancer and to identify clinicopathological features associated with USP7 expression.
PubMed, Scopus, Web of Science Core Collection, Wiley Online Library, and Google Scholar were searched from inception to July 2020. Pooled hazard ratios were calculated to evaluate the association between USP7 expression and overall survival (OS). In addition, pooled odds ratios were calculated to identify clinicopathological features associated with USP7 expression.
Eight studies in China were included in our meta-analysis, which had a total of 1192 patients and assessed five types of cancer. The pooled results revealed that a high expression of USP7 was associated with poor OS, especially in epithelial ovarian cancer (EOC). Moreover, USP7 expression was increased in patients with tumour-node-metastasis (TNM) stages III-IV, poor pathological grade, and positive lymph node metastasis. For patients with EOC, a high USP7 expression positively correlated with lymph node metastasis.
A high USP7 expression may promote cancer progression and predict unfavourable prognosis of cancer patients, especially those with EOC. Our findings suggest that USP7 inhibitors might be promising therapeutics for cancer patients with such characteristics.
许多研究都探讨了泛素特异性蛋白酶 7(USP7)在癌症中的预后价值,但结果仍存在争议。使用的评估检测方法(mRNA/蛋白)的差异可能是一个潜在的混杂因素。因此,我们提取了测量蛋白表达的研究,并进行了荟萃分析,以评估 USP7 表达在癌症中的预后作用,并确定与 USP7 表达相关的临床病理特征。
从建库到 2020 年 7 月,我们在 PubMed、Scopus、Web of Science Core Collection、Wiley Online Library 和 Google Scholar 上进行了检索。计算合并风险比来评估 USP7 表达与总生存期(OS)之间的关联。此外,还计算了合并优势比来确定与 USP7 表达相关的临床病理特征。
我们的荟萃分析纳入了中国的 8 项研究,共纳入 1192 名患者,评估了 5 种癌症。汇总结果表明,USP7 高表达与 OS 不良相关,尤其是在卵巢上皮癌(EOC)中。此外,USP7 表达在 TNM 分期 III-IV、病理分级差和阳性淋巴结转移的患者中增加。对于 EOC 患者,USP7 高表达与淋巴结转移呈正相关。
USP7 高表达可能促进癌症进展,并预测癌症患者预后不良,尤其是那些患有 EOC 的患者。我们的研究结果表明,USP7 抑制剂可能是具有这些特征的癌症患者的有前途的治疗方法。