Zoa Alexis, Yang Yingjie, Huang Wenjin, Yang Jing, Wang Jiangping, Wang Haibo, Dong Minghua, Tian Yuantong
Department of Pharmacology, School of Pharmacy and Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases, Gannan Medical University, Ganzhou, China.
School of Rehabilitation and Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases, Gannan Medical University, Ganzhou, China.
Transl Cancer Res. 2022 Sep;11(9):3080-3091. doi: 10.21037/tcr-22-787.
Hypoxia-inducible factor 1-alpha (HIF-1α) is overexpressed in pancreatic ductal adenocarcinomas (PDACs). However, the prognosis of high expression of HIF-1α in PDACs remains controversial because of lacking a solid support. A meta-analysis may help for a better understanding of the role of HIF-1α in the prognosis of PDACs.
By using a systematic approach, we conducted a meta-analysis from current literature. We performed an advanced search in PubMed, Embase, Cochrane Library and Web of Science databases. Recorded studies were published between September 1, 2001, and February 26, 2021, in English and related to the expression of HIF-1α in PDAC. We pooled and combined hazard ratios (HRs) and 95% confidence intervals (CIs) to show the effect of HIF-1α expression on overall survival (OS). We pooled also risk ratios (RRs) and 95% CIs to assess the correlation between HIF-1α expression and clinicopathological characteristics in PDAC. We evaluated publication bias among included studies through the Begg's test and Egger's test. From "Expression Plots" modules in the Gene Expression Profiling Interactive Analysis (GEPIA) database, we showed the difference of mRNA level for HIF1A between 179 pancreatic adenocarcinomas (PAADs) and 171 normal pancreatic tissues.
This meta-analysis included 11 studies and 764 patients. High expression of HIF-1α was associated with shorter OS compared to low HIF-1α expression in PDAC (HR =1.74, 95% CI: 1.49-2.04, P<0.001). Patients with high expression of HIF-1α tended to have an increased risk of earlier lymph node metastasis (LNM) (RR =1.63, 95% CI: 1.36-1.95, P<0.001), and more advanced clinical stage (RR =1.64, 95% CI: 1.38-1.97, P<0.001) compared to those with low HIF-1α expression. Expression plots from GEPIA database showed HIF1A overexpressed in PDAC tissues compared to normal tissues (LogFC =2, P<0.01).
High HIF-1α expression associated with worse prognosis of PDACs compared to low HIF-1α expression. Since HIF-1α expression is greater in PDAC than normal pancreas, it could serve as a prognostic factor and potential therapeutic target. However, due to the complex role of HIF-1α in physiology and pathology, therapeutic intervention should be considered with caution.
缺氧诱导因子1α(HIF-1α)在胰腺导管腺癌(PDAC)中过表达。然而,由于缺乏确凿的证据支持,HIF-1α在PDAC中高表达对预后的影响仍存在争议。荟萃分析可能有助于更好地理解HIF-1α在PDAC预后中的作用。
我们采用系统的方法,对当前文献进行荟萃分析。我们在PubMed、Embase、Cochrane图书馆和Web of Science数据库中进行了高级检索。纳入的研究发表于2001年9月1日至2021年2月26日之间,语言为英文,且与HIF-1α在PDAC中的表达相关。我们汇总并合并风险比(HR)和95%置信区间(CI),以显示HIF-1α表达对总生存期(OS)的影响。我们还汇总风险比(RR)和95%CI,以评估HIF-1α表达与PDAC临床病理特征之间的相关性。我们通过Begg检验和Egger检验评估纳入研究中的发表偏倚。从基因表达谱交互分析(GEPIA)数据库的“表达图谱”模块中,我们展示了179例胰腺腺癌(PAAD)与171例正常胰腺组织中HIF1A mRNA水平的差异。
该荟萃分析纳入了11项研究,共764例患者。与低HIF-1α表达相比,PDAC中HIF-1α高表达与较短的OS相关(HR =1.74,95%CI:1.49-2.04,P<0.001)。与低HIF-1α表达的患者相比,HIF-1α高表达的患者发生早期淋巴结转移(LNM)的风险增加(RR =1.63,95%CI:1.36-1.95,P<0.001),且临床分期更晚(RR =1.64,95%CI:1.38-1.97,P<0.001)。GEPIA数据库的表达图谱显示,与正常组织相比,PDAC组织中HIF1A过表达(LogFC =2,P<0.01)。
与低HIF-1α表达相比,HIF-1α高表达与PDAC预后较差相关。由于HIF-1α在PDAC中的表达高于正常胰腺,它可作为一个预后因素和潜在的治疗靶点。然而,由于HIF-1α在生理和病理中的作用复杂,治疗干预应谨慎考虑。