Li Zehan, Xu Shengchao, Chen Lin, Huang Shuqi, Kuerban Xieyida, Li Tianyu
The Department of Surgery, the First Dongguan Affiliated Hospital of Guangdong Medical University, Guangdong, China.
The Department of Surgery, Guangzhou Medical University, Guangdong, China.
Front Oncol. 2023 Feb 9;13:1090860. doi: 10.3389/fonc.2023.1090860. eCollection 2023.
It has been reported that ING3 inhibits the progression of various cancers. However, some studies have shown that it promotes the development of prostate cancer. The purpose of this study was to investigate whether ING3 expression is associated with the prognosis of patients with cancer.
PubMed, Cochrane Database, Embase, Medline, ScienceDirect, Scopus and Web of Science were searched until September 2022. The hazard ratio (HR)/odds ratio (OR) and 95% confidence interval (95% CI) were calculated using Stata 17 software. We used the Newcastle-Ottawa Scale (NOS) to assess the risk of bias.
Seven studies involving 2371 patients with five types of cancer were included. The results showed that high expression of ING3 was negatively associated with a more advanced TNM stage (III-IV vs. I-II) (OR=0.61, 95% CI: 0.43-0.86), lymph node metastasis (OR=0.67, 95% CI: 0.49-0.90) and disease-free survival (HR=0.63, 95% CI: 0.37-0.88). However, ING3 expression was not associated with overall survival (HR=0.77, 95% CI: 0.41-1.12), tumor size (OR=0.67, 95% CI: 0.33-1.37), tumor differentiation (OR=0.86, 95% CI: 0.36-2.09) and gender (OR=1.14, 95% CI: 0.78-1.66).
This study showed that the expression of ING3 was associated with better prognosis, suggesting that ING3 may be a potential biomarker for cancer prognosis.
https://www.crd.york.ac.uk/prospero/, identifier (CRD42022306354).
据报道,ING3可抑制多种癌症的进展。然而,一些研究表明它会促进前列腺癌的发展。本研究的目的是调查ING3表达是否与癌症患者的预后相关。
检索了截至2022年9月的PubMed、Cochrane数据库、Embase、Medline、ScienceDirect、Scopus和Web of Science。使用Stata 17软件计算风险比(HR)/比值比(OR)及95%置信区间(95%CI)。我们采用纽卡斯尔-渥太华量表(NOS)评估偏倚风险。
纳入了7项研究,涉及2371例患有5种癌症的患者。结果显示,ING3高表达与更晚期的TNM分期(III-IV期vs. I-II期)(OR=0.61,95%CI:0.43-0.86)、淋巴结转移(OR=0.67,95%CI:0.49-0.90)及无病生存期(HR=0.63,95%CI:0.37-0.88)呈负相关。然而,ING3表达与总生存期(HR=0.77,95%CI:0.41-1.12)、肿瘤大小(OR=0.67,95%CI:0.33-1.37)、肿瘤分化(OR=0.86,95%CI:0.36-2.09)及性别(OR=1.14,95%CI:0.78-1.66)无关。
本研究表明,ING3表达与较好的预后相关,提示ING3可能是一种潜在的癌症预后生物标志物。